#sop-software-sample

[3plinsight]

How to Ensure Accurate Sample Receiving in 3PL Warehouses

Proper sample receiving in 3PL warehouses ensures quality checks, accurate labeling, and updated inventory. Following a clear SOP prevents mix-ups and supports traceability. See how a structured approach improves efficiency. Learn more about 3PL Labor Planning Software at 3PLInsight https://3plinsight.com/sample-receiving-sops/

[batchmasteruk]

Pharmaceutical ERP Systems: A Complete Solution for UK-Based Companies

The pharmaceutical industry faces challenges such as stringent regulatory compliance (MHRA, GMP, FDA), rising R&D and production costs, supply chain disruptions, counterfeit drugs, and growing competition from generics and biosimilars. Additionally, sustainability concerns, digital transformation, and cybersecurity risks add complexity. To overcome these, companies must adopt robust Pharmaceutical ERP systems, tracking solutions and sustainable manufacturing practices to enhance efficiency, compliance, and market competitiveness. 

Here’s how: 

Key Features of Pharmaceutical ERP Systems 

1. Managing Compliance 

Pharmaceutical ERP software ensure adherence to UK and EU regulations, including Good Manufacturing Practice (EU GMP) guidelines and Medicines and Healthcare Products Regulatory Agency (MHRA) requirements. 

Such solution even support 

✔ Electronic signatures  ✔ Approval controls  ✔ Audit trail   ✔ Document control & SOP (Standard Operating Procedure) management  ✔ Certification or Supplier management 

2. Batch Resizing 

The ERP system facilitates dynamic batch resizing, enabling manufacturers to adjust batch sizes in real-time based on available raw materials or specific order requirements. This optimises resource utilisation and production workflows from batch creation to allocation, material issue, quality inspection, batch QC, batch ticketing, label printing, WIP management, cost calculations, yield analysis, and final batch closure—ensuring efficiency and compliance at every stage. 

3. Bi-Directional Traceability 

Maintaining strong product safety and recall protocols, a pharmaceutical ERP software provides end-to-end lot tracking—from raw material procurement to production and finished goods delivery, and vice-versa. This guarantees complete visibility across the supply chain and enables a quick response in the event of quality issues or recalls. 

4. Automated Labelling & Report Generation 

Pharmaceutical ERP facilitates automated chemical content labelling with label printing capabilities. It also generates essential labels and reports, including:  ✔ FDA labels and reports  ✔ Batch Manufacturing Record (BMR)  ✔ Master Batch Record (MBR)  ✔ Certificate of Analysis (COA) 

All reports adhere to industry-defined standards and formats. 

5. Streamlining Inventory Management 

An ERP system ensures optimal inventory levels, helping manufacturers avoid overstocking and understocking, thereby improving material availability and profitability. 

With real-time inventory visibility and material requirement planning, ERP software prevents supply chain disruptions. It also supports various inventory optimisation methods, LIFO, FIFO, FEFO, etc., and different costing methods like Standard, Market, Average, and such. 

Additionally, it tracks shelf life and expiration dates accurately, support classification and characteristic definition, tracks to Palleted, Bin, Lot and Item level, ensuring optimal material utilisation, reducing waste, and enhancing overall efficiency. 

6. Ensuring Quality Control 

ERP systems for pharmaceutical feature built-in quality management modules, allowing parameter-driven quality checks at every stage of production. Stability testing, user-defined sampling, maintaining test results in numeric/alphanumeric/pass-fail value, double testing etc., are other capabilities offered by Quality Control module of ERP software.  These checks and capabilities ensure that only compliant products reach the market, ensuring both- regulatory adherence and consumer safety. 

7. Handling Formulations 

The Formula Module in BatchMaster ERP for Pharma offers formula patenting, version control, and secure access to protect intellectual property. It enables real-time adjustments, automatic UOM conversions, and cost analysis for accurate formulation. The module also enable multiple packaging, ensures formula security, and approval workflows, enabling efficient and controlled formula management.  

8. Contract Manufacturing: 

ERP for Pharma industry supports and streamlines contract manufacturing and third-party/loan licensing scenarios through capabilities like separate inventory allocation, production with zero cost, inventory transfers, automated cost calculations, contract-based pricing, and invoicing for contract-manufactured goods, etc.  

Benefits of a Pharmaceutical ERP System 

With such industry-specific capabilities, the benefits pharma manufacturers reap upon using a Pharma ERP are many: 

✔ Reduced  risk of non-compliance  ✔ Keeps the organisation audit-ready  ✔ Enhances operational efficiency  ✔ Minimises waste  ✔ Secures sensitive pharmaceutical data and more. 

UK-Based Pharmaceutical Manufacturers—This Is for You! 

If you are looking for the above capabilities, invest your valuable time and resources in a powerful ERP like BatchMaster ERP for Pharmaceuticals. This industry-specific solution provides all the above-stated features along with: 

✔ Separate handling of soft gels, capsules, injections, etc.  ✔ Opportunity & sample management  ✔ Precise material & production planning  ✔ Manufacturing and material movement as per cGMP guidelines  ✔ GMP validation  ✔ Micro-verticalised ERP solutions for API, biotechnology, dietary supplements, vaccines, veterinary, and more 

With such comprehensive functionalities, BatchMaster ERP in UK is a complete solution for UK-based pharmaceutical manufacturers. 

[onlineeducation1]

Online MA in English Programs: Costs, Requirements, and Admission Tips

Pursuing an Online Master of Arts (MA) in English is an excellent way to deepen your knowledge of literature, language, and creative writing while maintaining the flexibility to balance your education with personal and professional commitments. This guide will explore the costs, admission requirements, and tips to help you navigate the application process for an online MA in English program.

Costs of an Online MA in English Program

The cost of pursuing an online MA in English can vary significantly depending on the institution, program structure, and geographic location. Here are some key factors to consider:

Tuition Fees

Tuition costs for online MA in English programs typically range from $10,000 to $30,000 for the entire program. However, some prestigious institutions may charge higher fees.

Additional Costs

Beyond tuition, students should budget for:

Technology fees

Course materials (e.g., textbooks, software subscriptions)

Graduation fees

Financial Aid and Scholarships

Many universities offer financial aid packages, scholarships, and grants for online students. Researching these opportunities can significantly reduce the financial burden.

Employer Sponsorship

Some employers may sponsor or reimburse tuition costs if the program aligns with your current job role or career goals.

Admission Requirements for an Online MA in English Program

Admission requirements for an online MA in English program vary by institution, but common prerequisites include:

Academic Qualifications

A bachelor’s degree from an accredited institution is mandatory. While a BA in English or a related field is preferred, some programs accept students with degrees in other disciplines.

Minimum GPA

Most programs require a minimum GPA of 3.0 on a 4.0 scale. However, some universities may consider lower GPAs with strong supplemental materials.

Letters of Recommendation

Applicants typically need 2-3 letters of recommendation from professors, employers, or mentors familiar with their academic or professional abilities.

Statement of Purpose (SOP)

A well-crafted SOP outlining your academic interests, career goals, and reasons for pursuing the program is essential.

Writing Sample

Many programs require a writing sample to assess your analytical and writing skills. This is often a critical essay, research paper, or creative work.

Language Proficiency (for International Students)

Non-native English speakers must demonstrate proficiency through tests like TOEFL or IELTS.

Admission Tips for Success

Navigating the admission process can be challenging, but the following tips will help you stand out as a strong candidate:

Start Early

Begin researching programs and preparing application materials 6-12 months before the application deadline to avoid last-minute stress.

Tailor Your Application

Customize your SOP and writing sample to reflect the specific strengths and focus areas of the program you are applying to.

Leverage Recommendations

Choose recommenders who can provide detailed and personalized insights into your academic or professional strengths.

Highlight Relevant Experience

Showcase internships, teaching experience, publications, or other achievements that demonstrate your commitment to the field of English.

Proofread and Revise

Carefully review your application materials for errors. Consider seeking feedback from mentors or peers.

Engage with Admissions Counselors

Reach out to program representatives with questions or to express interest. Building a relationship can leave a positive impression.

Final Thoughts

An online MA in English offers a flexible and enriching opportunity to advance your education and career. By understanding the costs, meeting the admission requirements, and strategically preparing your application, you can set yourself up for success. Whether your goal is to teach, write, or explore literature at a deeper level, this program can be a stepping stone to achieving your ambitions.

[improvingveterinarydiagnostics]

Ensuring Accuracy and Reliability in Veterinary Diagnostic Test Results

Veterinary diagnostic companies employ several measures to ensure accuracy and reliability in their test results:

1. Quality Control (QC) Procedures:

Regular calibration and maintenance of equipment

Use of certified reference materials

Internal quality assurance programs

2. Standardized Operating Procedures (SOPs):

Well-defined protocols for sample handling, testing, and analysis

Training programs for personnel

3. Accreditation and Certification:

Compliance with international standards (e.g., ISO/IEC 17025)

Accreditation by reputable organizations (e.g., AAVLD, NVLAP)

4. Proficiency Testing:

Participation in external proficiency testing programs

Comparison with peer laboratories

5. Validation and Verification:

Validation of new tests and instruments

Verification of test performance characteristics

6. Sample Handling and Storage:

Proper sample collection, storage, and transportation

Minimization of sample contamination and degradation

7. Data Management and Analysis:

Use of validated software and algorithms

Automated data analysis and reporting

8. Continuous Education and Training:

Regular updates on new technologies and methodologies

Continuing education for personnel

9. Interlaboratory Comparisons:

Collaboration with other laboratories

Comparison of results to ensure consistency

10. Customer Feedback and Complaint Resolution:

Monitoring customer satisfaction

Addressing concerns and resolving issues promptly

By implementing these measures, veterinary diagnostic companies ensure accurate and reliable test results, supporting informed decision-making in animal healthcare.

[tracetassetmanagment]

Enhancing Business Efficiency with the Quality Management Module in Udyog ERP — Best ERP Software in India

In today’s competitive market, maintaining product and service quality is crucial for businesses to thrive. The Quality Management (QM) module in Udyog ERP, the best ERP software in India, plays a vital role in ensuring that products meet predefined standards and customer expectations. It empowers organizations to streamline quality processes, reduce defects, and maintain compliance with industry standards.

Quality planning sets the foundation for ensuring high standards across production. The best ERP software in India, Udyog ERP, enables businesses to define inspection plans, set up sampling procedures, and establish clear quality goals. By utilizing this module, companies can ensure that all products align with the necessary quality standards from the start.

With Udyog ERP’s Quality Inspection feature, businesses can perform real-time inspections during various production phases. This component allows for accurate capturing of results, managing defects, and adhering to quality plans, ensuring that Udyog ERP maintains its reputation as the best ERP software in India.

By leveraging Udyog ERP’s Quality Control capabilities, businesses can monitor and regulate production processes to ensure consistency. The best ERP software in India offers tools that allow for continuous tracking and corrective measures, minimizing errors and waste.

Udyog ERP goes beyond just product inspection by focusing on quality assurance. This module ensures that preventive measures, audits, and reviews are built into the process, emphasizing that quality is not an afterthought but an integral part of production. That’s why Udyog ERP is known as the best ERP software in India for improving quality control.

Managing supplier quality is crucial for maintaining the final product’s standard. Udyog ERP helps ensure that suppliers comply with quality standards through audits, inspections, and issue tracking, solidifying its position as the best ERP software in India for comprehensive supply chain management.

Maintaining up-to-date quality documents is essential for smooth operations. Udyog ERP’s Document Control feature manages reports, SOPs, and instructions efficiently. This functionality guarantees that businesses using the best ERP software in India can always access accurate, updated documentation.

The reporting and analytics capabilities in Udyog ERP offer deep insights into quality performance. By generating detailed reports, businesses can identify trends, make informed decisions, and drive continuous improvement, ensuring Udyog ERP remains the best ERP software in India for businesses aiming for excellence.

Benefits of Implementing a Quality Management Module in Udyog ERP

Implementing the Quality Management Module in Udyog ERP, the best ERP software in India, provides businesses with a range of critical benefits. First, it ensures consistency in product quality, helping companies meet both customer expectations and regulatory standards with ease. Additionally, Udyog ERP aids in achieving full compliance with industry regulations, reinforcing its standing as the best ERP software in India for adhering to strict quality requirements.

By reducing waste and minimizing rework, the system also leads to significant cost savings. With enhanced quality control, businesses’ experience improved customer satisfaction and loyalty, further solidifying Udyog ERP’s reputation. The module’s ability to detect potential quality risks early on allows for timely corrective actions, preventing costly errors. Moreover, it fosters continuous improvement, providing a structured approach to ongoing quality enhancements, which drives innovation and ensures long-term competitiveness in the market.

[mim-essay]

Crafting Your Future: Effective SOP Samples for MBA Applications

Introduction

An essential part of your MBA application is a Statement of Purpose (SOP). It functions as a personal story outlining your objectives, experiences, and driving forces. You may differentiate yourself from other candidates with a strong SOP, so take the time to carefully develop a fascinating story. This article will explain the value of SOP samples for MBA applications and show you how to write a compelling statement.

What Makes a SOP Vital?

Personal Insight: You can highlight aspects of your character, ideals, and distinctive experiences with a SOP that are not possible to do with just grades or numbers. It gives admissions officers a more comprehensive picture of your personality.

Motivation and Objectives: This paper explains your motivations for wanting to get an MBA and how they relate to your goals with your goals for your career. Setting clear objectives can show your dedication and forethought.

Writing Skills Reflection: Your SOP shows how well you can communicate as well. Making a strong impression requires coherence, clarity, and an engaging story.

Important Elements of a Robust SOP Overview: Start with an attention-grabbing hook to draw the reader in. This could be a quotation, anecdotal evidence, or a memorable event that influenced your professional goals.

Academic Background: Give a brief rundown of your school history. Emphasize any initiatives, coursework, or accomplishments that have helped you get ready for an MBA.

Professional Experience: Talk about your previous employment, highlighting any positions that had an impact on your decision to pursue an MBA. Emphasize your individual successes and acquired talents.

Career Objectives: Clearly articulate your immediate and long-term professional goals. Describe how you plan to accomplish these goals with the support of the MBA program you are applying to.

Compatibility with the Scheme: Examine the particular MBA program and provide evidence for why it is a good fit for you. Mention the instructors, the courses, or the special chances that drew you to the university.

Conclude by restating your primary ideas and reiterating your excitement for the course. Make a lasting impression by restating your dedication to both career and personal development.

SOP Framework Examples

Although your SOP should be specific to your experiences, you can be inspired by the following sample frameworks:

First Example: The Career Shifter

"As a software engineer, I never saw myself in the finance industry until I oversaw a project that demonstrated the significance of financial strategy," the introduction reads Academic Background: Emphasize your engineering degree and any applicable economics education.

Professional Experience: Talk about the technical responsibilities you held and how they sparked your curiosity about finance.

Career aspirations: "I hope to use my technical background to transition into investment banking."

Fit with the Program: Share a faculty member or financial course that you particularly like.

reiterate your enthusiasm for the marriage of technology and money.

Last Words on Writing Your SOP

Be True to Yourself: Your SOP ought to represent who you really are. Write in a style that comes naturally to you and stay away from clichés.

Be Particular: Employ concrete Give examples to support your arguments. Your story may suffer from vague statements.

Get Input: After you've written your SOP, ask mentors, colleagues, or experts in the admissions process for their input.

Edit & Revise: Make sure there are no grammatical issues and that your SOP makes sense. A well-written document exudes professionalism.

Summary

Creating a compelling SOP for your MBA application is a chance to highlight your goals and unique style. You can create an engaging story that appeals to admissions committees by using SOP samples as a model. Recall that this is your opportunity to share your experience; make it stand out! Your SOP can be an effective instrument in helping you reach your academic and professional objectives if it is carefully planned and truly reflected upon.

[sudheervanguri]

Lupin Ltd, a global pharmaceutical company renowned for its high-quality products and innovative research, is organizing a walk-in interview for various positions in Quality Assurance, Quality Control, and Production. This recruitment drive offers an excellent opportunity for professionals with the right qualifications and experience to join a leading company committed to excellence in pharmaceutical manufacturing. Vacancy Details and Qualifications 1. Quality Assurance - Officer/Associate Experience: 2-4 Years Qualification: BSc (Chemistry) Skills Required: Relevant experience in Quality Assurance, including Sampling activity, IPQA, QAMS, Documentation, and Review of BPR. Proficiency with Quality-QAMS software. Job Location: Tarapur, Maharashtra 2. Quality Control - Officer/Associate Experience: 2-4 Years Qualification: BSc (Chemistry/Analytical) Skills Required: Experience in Quality Control Lab with hands-on expertise in handling instruments like HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), and KF (Karl Fischer). Knowledge of GLP (Good Laboratory Practice), GDP (Good Documentation Practice), lab safety, and LIMS (Laboratory Information Management System) software. Job Location: Tarapur, Maharashtra 3. Production - Sr. Officer/Officer/Associate Experience: 2-6 Years Qualification: MSc, BSc, Diploma - Chemical Skills Required: Proven experience in working with Pharma-API plants, adhering to SOPs (Standard Operating Procedures), meeting production targets, and maintaining safety practices. Ability to handle and analyze process problems in manufacturing with a sound knowledge of operations involving centrifuges and reactors. Job Location: Tarapur, Maharashtra [caption id="attachment_58299" align="aligncenter" width="930"] Lupin Ltd Walk-In Interview for Quality Assurance, Quality Control, and Production[/caption] Interview Details Dates & Time: Bharuch, Gujarat: 30th August 2024 (Friday), 10:00 AM to 2:00 PM Ambernath, Thane: 31st August 2024 (Saturday), 10:00 AM to 2:00 PM Venues: Bharuch: Hotel Ginger, Railway Station Rd, Opp. Patel Super Market, Moficer Jin Compound, Bharuch, Gujarat 392001 Ambernath: Hotel Krishna Palace, P 35/36, Anand Nagar, Additional M.I.D.C, Ambernath, Thane-Maharashtra 421503 Candidates who meet the qualifications are encouraged to attend the walk-in interviews. Please bring your updated resume, relevant certificates, and other necessary documents. For any queries, feel free to contact 7391040115 or send your profile to prachipatil@lupin.com.

[futuristictalefart]

Figure out how to organize a SOP for MS in software engineering from the actual specialists. Additionally, get tips and observe the normal slip-ups made by understudies.

[orthonathanganol]

Nathanael Warner

Brooklyn, NY, 11205                                        clevonwarner96@outlook.com 929-665-4506                  

__________________________________________________________________________________________________

SUMMARY:

Laboratory Technician with experience in device testing, food and drug testing and data analysis.

Research Assistant with experience in neuromodulation research & compound synthesis.

Seeking an intermediate position in an academic or industry laboratory.

__________________________________________________________________________________________________

EDUCATION:

Bachelor’s of Science, Chemistry, Howard University, 2019

Neuromodulation & Neuroimaging, UCLA, California, 2018

Associates Degree in Environmental Science, Presentation College, 2014

__________________________________________________________________________________________________

EXPERIENCE:

Title: Engineering Technician

Employer: Felix Storch Inc/Summit Appliances | 2022 - 2023

      770 Garrison Street, Bronx, NY 10474

~ Quality Assurance for Home and Medical Appliances

~ Ensured temperature compliance of refrigerators and freezers

~ Created reports on energy usage and efficiency.

~ Created labels for manufacturing and shipping departments.

~ Microsoft Access and Excel used for data and inventory management.

__________________________________________________________________________________________________

Title: Wearable Safety Technician

Employer: Google | 2020 – 2021

      40 Jessie Street, San Francisco, CA, 94105

<> Safety Testing for Smart Accessories 

<> Tested watch materials for the presence of skin irritants using GC/LC and ICP MS.

<> Created large volumes of artificial sweat, buffer solutions and solvents.

<> Performed lab maintenance tasks including ordering reagents and glassware.

<> Trained in lab’s safety, SOP, GDP and cGMP.

<> Python and Google Workspace used for data and inventory management.

__________________________________________________________________________________________________

Title: e-Commerce Shopper

Employer: Safeway Supermarket | Winter 2020 

    2020 Market St, San Francisco, CA 94114

Online Order Fulfillment

Completed online grocery orders for Safeway’s Drive Up and Go customers during COVID-19.

Able to work the frontend and backend of food retail environments.

Interacted directly with customers and worked with leadership to correct any problems.

Trained on inventory software for warehouse and retail.

__________________________________________________________________________________________________

Title: Food & Drugs Sample Technician

Employer: Element Materials Technology | 2019 – 2020

      9240 Santa Fe Springs Rd, Santa Fe Springs, CA, 90670

Heavy Metals Sample Testing

Prepared food and drug samples for heavy metals testing using ICPMS

Dissolved compounds via microwave superheating & acid/base digestions.

Tracked jobs, samples and reagents using 3rd party laboratory information management system.

Trained in lab’s safety, SOP, GDP and cGMP.

__________________________________________________________________________________________________

Title: Research Assistant

Employer: University of California, Los Angeles | 2018

    Semel Institute

    760 Westwood Plaza, Suite 57-430, Los Angeles, CA 90024

Spatial Navigation EEG Data in Humans

Spike sorted signals from electrodes implanted in the medial temporal lobes of patients being treated for epileptic seizures.

Identified theta modulations in brain wave activity during imagined activity as well as during real world movement.

EEG data analyzed using the wav_clus and MATLAB libraries for Python.

__________________________________________________________________________________________________

Title: Research Intern

Employer: Howard University | 2017 - 2019

    College of Pharmacy, 

    2201 Georgia Avenue, NW Washington, D.C. 20059

R&D for Turmeric Based Therapeutic Compounds 

Researched the curcumin molecule contained in turmeric.

Found that curcumin suppressed inflammatory responses in the brain and joints. 

Synthesized analogs of curcumin,  generally using Suzuki-Coupling mechanisms.

__________________________________________________________________________________________________

Title: Polymer Chemist

Employer: Global Marketing Enterprise | 2014 - 2015

   9 Fourth Street, Gasparillo, Trinidad and Tobago

Plastics Manufacturing 

Supervised recycling of plastics, transforming processed materials into pellets

Petrochemical research investigating environmentally safe methods to degrade polymers 

__________________________________________________________________________________________________

SKILLS

Formulations, microscopy, spectroscopy, separations, dilutions and other basic laboratory technique

Trained in cGMP, GLP and GDP

Computer programming - Python, HTML and some C++

Google Workspace & Microsoft Office

Fluent in French

[scispot]

Scispot - GUI and CLI first ELN plus LIMS for fast growing bio startups

Scispot - GUI and CLI first ELN plus LIMS for fast growing bio startups

Top 5 Essential Features For Lab Management Software

The global laboratory information management system market size, valued at 1.85 Billion USD in 2021, is growing rapidly at a compound annual growth rate (CAGR) of 7.0% from 2022 to 2030.

The high demand for laboratory information management systems is the result of technological advancements pertinent to life science laboratories, stringent regulatory requirements and the rising interest in lab automation.

However, there are hundreds of lab management software in the market, leaving the lab managers, lab informatics teams and scientists overwhelmed with options.

To help you choose the best lab management software, we've listed 5 must-haves every lab should expect from their lab software vendors.

1. Templates for repeatable research and operational processes Every lab needs to have standardized workflows to ensure reproducibility of their experiments, eliminate experiment error rates, preserve institutional knowledge and increase the output. The lab management software you’re using should be able to make templates of your repeatable protocols, experiments, standard operating procedures and even operational processes such as approval flows, multi-well plates, request forms, notifications rules and much more. Scispot makes all of this possible by allowing you to drag & drop pre-populated protocols or SOP templates and set automation rules to prepare your R&D projects with unrivaled speed.

2. Strong framework for internal and external collaboration Lab work is a team effort. You need to be able to collaborate, notify and selectively invite your labmates, partners, customers, and vendors (e.g., CROs, core labs, etc.) so that research is done the right way. Keeping everyone up to date on Scispot is a cinch. Scispot helps you to collaborate with your customers or CROs on R&D projects and share the results in no time flat.

3. Global search functionality for instant data access Storing data is hardly of any use if you can't easily find your data, filter it and make correlations to extract essential insights on a daily basis. With the right lab management system, you should be able to retrieve information at a moment’s notice using different parameters such as samples, customers, partners, experiments, locations, instruments, project, file type, etc.

4. Compatibility with 3rd-party apps & your legacy systems to centralize data in one spot The most important asset of any lab is its data. However, the data only becomes valuable when it is structured correctly, machine-readable and has all the context associated with it -- for this to happen, you need to bring in data from multiple sources and connect them with the proper context. Your lab management software should be able to centralize data from 3rd-party apps, your legacy systems and instruments. Scispot connects with hundreds of 3rd-party apps (Hubspot, Google Sheets, Shopify, etc.) and legacy systems (ELN, LIMS, LES, etc.) to unify all of your data in one spot.

5. A wide array of customizable and configurable offerings Every life science company is unique, so lab software should be able to adapt to the diverse scientific needs of each one. You cannot and should not use a rigid off-the-shelf product like ELN (electronic lab notebook) and LIMS (lab information management system).

‍ Scispot offers no-code configuration, a developer toolkit and custom engineering support to personalize the platform for every life science company -- be it a contract research organization (CRO), industrial biotech company or biomanufacturer. Scispot is more than a LIMS or ELN platform. It is fully configurable, highly intuitive and completely integratable with other 3rd-party tools such as Google Sheets and Asana.

[sop-writingsamples-blog]

SoP Software Sample

Great SOP software sample that will help you elevate your SOP onto another level. For more samples like this, follow this link http://www.sopwriting.net/try-this-sop-for-ms-in-computer-science/

[gubgam]

Yessssss. Also, SOPs (Standard Operating Procedures), which are intricately detailed guides by people who work in the lab, on the same equipment, same software (with screenshots and pictures 💕) and worked together to cover every button you press on this machine, every color your sample could turn etc etc. I love them. They are changed and updated as well. You’re ENCOURAGED to work with them out. It’s just so good. If I forget directions no worries! They’re here! I don’t have to feel imposter syndrome when I forgot how to set a micrometer! There was a detailed guide!

i might just be autistic but data entry fucking rules dudes you just. enter the data. you take the data and you plug it in. then what? who knows! who cares. the data. has been entered. what next? buddy you’re not gonna believe this it’s more fucking data. excel used to be my enemy but now she is my best friend

[free-lims]

3 Tech Trends in Environmental Testing to be on the Lookout for

The field of environmental testing has evolved significantly in the last decade and alongside it, the pressure to adapt to the shift has landed squarely on laboratories that test environmental samples. Laboratories need to perform a diverse range of analytical tests on environmental samples such as air, water, soil, and wastes (liquids, solids, or sludges). At the same time, laboratories have not been spared the economic upheavals that have cut across industries following the pandemic-initiated global recession. This has come with market consolidation and declining profitability. However, things are not as bad as they may seem. The market size for environmental testing is expected to surpass $17 billion by 2030, from $8 billion in 2023. What laboratories need is a lifeline to tide them over the recession period and accelerate productivity. In this case, leveraging technology seems to be it.

Here are three technological trends that are expected to gain momentum in 2023 and thereafter.

1. Automation of Laboratory Processes

While most environmental laboratories have already adopted some form of automation, we expect to witness an even greater uptake in 2023 and beyond.

Environmental laboratories face a myriad of challenges including the need to cut back on operational costs as well as a shortage of skilled and competent staff. At the same time, it is expected that the demand for environmental testing will grow exponentially in terms of volume and diversity of tests. Furthermore, environmental testing laboratories need to follow several regulatory guidelines such as NELAC (TNI), ISO 17025, RCRA, CERCLA, GLP/GALP, UCMR, CFR Title 40, CWA, NPDES, RCRA, UIC, besides state and local regulations. Managing huge volumes of test requests and data generated from them while meeting regulatory compliance can be overwhelming. This has created the need for informatics solutions.

Increasingly, more and more environmental testing laboratories are opting to automate entire workflows to maintain data integrity and eliminate manual errors. This includes processes associated with samples, tests, and data management as well as management of lab instruments, software, Standard Operating Procedures (SOPs) and personnel.

Automation presents several benefits, including data accuracy, the efficiency of processes as well as increased output. It also reduces the administrative workload and allows laboratory staff to focus on more specialized tasks. While the initial cost of switching from manual processes to automated systems can be high, this is likely to yield higher returns in terms of profits in the long run. Fortunately, automation technology for laboratories is now widely available, and consequently, automation has become relatively affordable for even small laboratories with meager budgets.

2. Cloud Computing

Cloud computing supports automation by providing remote and secure access to several IT resources that are hosted in the cloud. A survey conducted by Environmental Business International (EBI) showed that over 50% of environmental companies are planning to invest in cloud computing (IoT) in the 2020s.

Cloud computing allows laboratories to access computing services such as servers, databases, and software over the Internet. It enables real-time collaboration and cost-saving through economies of scale. Laboratories can easily store and access data from any location and at any time. Modern in-the-cloud systems, such as a cloud-based Laboratory Information Management System (LIMS), use world-class technology to beef up security and provide automated timely security updates. In multi-laboratory companies, a LIMS can centrally store data of all laboratories and manage diverse workflows of all laboratories, thereby eliminating data silos.

3. Artificial Intelligence (AI) and Machine Learning (ML)

AI empowers computers with the ability to “think” and execute actions without human input. Environmental testing laboratories can leverage AI and ML to improve experimental design, quickly analyze test results of multiple tests, and make data-driven decisions that may take days if done manually. Just like automation, AI reduces human error in laboratory processes and boosts productivity. The Environmental Business International (EBI) survey showed that over 50% of environmental laboratories are planning to invest in AI.

Apart from AI, the integration of LIMS with Augmented Reality (AR) and Mixed Reality (MR) solutions helps environmental testing laboratories to see SOPs and record observations. All these technologies are intended to increase efficiency in laboratories and boost output in tandem with the demands of 21st-century environmental testing.

A Greater Demand for an Environmental LIMS Software

From a value of $1.85 billion in 2021, the LIMS industry is expected to reach a value of $3.5 billion by 2030, growing at a CAGR of 7%. In a survey that was conducted by EBI, 95% of environmental companies indicated that they have the intention to invest in a LIMS. Most of these companies strongly believe that information technology is necessary for digitally transforming lab operations and for the evolution of the industry to the next phase. An environmental LIMS software automates laboratory workflows by integration with all instruments and software and ties in with other technological trends such as AI and ML.

A LIMS also manages and streamlines the entire sample life cycle, from sample accessioning to reporting test results to customers and regulatory agencies. Furthermore, a LIMS enables laboratories to meet stringent regulatory guidelines, flag out-of-specification results, analyze trends across a set of samples, track deviations from SOPs, and centrally manage multi-laboratory data with ease.

Leveraging The Latest Tech Trends Using an Environmental LIMS Software

Environmental testing is a profitable and competitive niche, but with a fair share of challenges at the same time. Forward-thinking laboratories can use the latest technology trends to pivot their operations so they can meet the stringent demands of environmental testing. Tech trends to be on the lookout for in the coming years include the automation of most laboratory processes, wide-scale adoption of cloud computing, and the use of artificial intelligence and machine learning. At the same time, more laboratories are expected to implement a cloud-based environmental LIMS software to digitally transform and future-proof their operations.

Originally published at https://freelims.org.

[iso9001registration]

Why is accreditation with ISO 17025  important?

A third party extensively assesses the laboratory's quality management system and technical proficiency in order to grant ISO 17025 Consultant cost in Bahrain accreditation. To keep accreditation, audits are carried out frequently. Only a recognized accreditation authority may grant ISO 17025 accreditation. In order to produce calibration and test results, a laboratory must meet both the management requirements and the technical requirements of ISO17025 in order to be accredited.

What are the benefits of ISO/IEC 17025 accreditation for testing laboratories?

Due to differences in personnel expertise, equipment used, and Standard Operating Procedures (SOPs) followed when performing the test, several analytical testing laboratories frequently generate different test findings for a particular sample. These differences result from the use of inaccurate and poorly maintained instruments, ambient conditions in the laboratory, and the skill level of the laboratory personnel conducting the test. The fabrication of potency reports to raise retail value is another factor contributing to this discrepancy. This is frequently accomplished by fiddling with test findings and sampling techniques. Well, a plethora of variables may be at play in the consistency and accuracy of test results and the conclusions drawn from them.

So, are there any rules a testing laboratory must abide by?

One such law that outlines specifications for testing facilities is ISO/IEC 17025. Accreditation to ISO/IEC 17025 is required for testing facilities in order to prove their technical proficiency and guarantee the reliability of test results. The importance of ISO/IEC 17025 accreditation for your laboratory will be highlighted in this article.

First of all, one of the most important accreditations for all kinds of laboratories, institutions, and research facilities that conduct tests and calibration is ISO/IEC 17025. A testing or calibration laboratory may cite ISO/IEC 17025 as the standard that best meets their management and technical needs. Additionally, accreditation by regulatory agencies attests to the reliability and accuracy of the results, which are produced in accordance with best practices.

Exactly why was ISO/IEC 17025 updated?

It is essential to stay abreast of revisions and modifications to the standard and to set up your lab for compliance.

Due to an increase in errors and inaccurate data, ISO/IEC 17025 was updated. To stay current with the industry and as nearly as possible adhere to the ISO 9001:2015 standard, ISO/IEC 17025 has already undergone two updates, the first in 2005 and the second in 2017.

The most recent adjustments to the laboratory environment and work procedures were made to ISO/IEC 17025. The most recent revisions to ISO/IEC 17025 add a new chapter on risk-based thinking, control over nonconforming testing and calibration operations, new terminology, incorporating computer systems, and tightening data control, among other things.

scope to incorporate sampling, calibration, and testing. New standards like ISO 9001 (quality management), ISO 15189 (quality of medical laboratories), and ISO/IEC 17021-1 now align with the process approach (which states the requirements for auditing and certification bodies).

Is obtaining ISO/IEC 17025 accreditation for your laboratory a difficult task?

The ISO 17025 standard is extensive and complex, thus it necessitates a full comprehension of and training in its application. Conducting routine internal audits to get a lab ready for third-party evaluations proves to be a huge difficulty because the goal is to standardize the operations of all testing laboratories and to assure the authenticity of the data collected. Finding a trustworthy and integrated software solution that aids in meeting the regulatory criteria is also difficult as well.

It is crucial to implement a Laboratory Information Management System (LIMS) that enables your laboratory to adhere to ISO 17025 Certification in Oman standards as well as other national, regional, and municipal laws.

[leetrevenaphd]

Latest activities

I have been testing the VR software ‘Sophie Social’ with friends and family. On the 24th of July 2022, I tested it with a Friend, and last night (2 Nov 2022) my Mum tried it out too.

The take away, from these two early tests, is that participants are likely to struggle with navigating through the VR environment and using the hand-held controllers, even more so if the participant is not technologically proficient. Moreover, whilst I am not expecting DSW participants to have Arthritis, my Mum does, in her hands, and therefore found the hand-held controllers difficult and uncomfortable to use.

It was interesting observing my Mum apologizing to Sophie (Avatar) numerous times throughout her VR experience, as my Mum struggled just steering through the environment. For example, as the avatar (Sophie) stood there continuingly pointing to a picture in the magazine she was holding, my mum kept apologizing to Sophie (Avatar).

These early tests also highlighted a need for an external review monitor. It was very difficult to guide the users in navigating, and I found myself wanting, and needing, to observe what is occurring in the VR environment. Indeed, having a review monitor for this, will be very useful, especially if the user is struggling to use the technology.  

I will be doing another test on the weekend of November the 12th 2022 with my friend. Prior to this, I aim to have an early and basic instruction guide developed to test out and see if it helps my friend navigate.

 In addition (to this), I emailed a couple of ABC journalists and was informed that Elizabeth Wright is the ABC’s disability affairs correspondent. I subsequently sent Elizabeth an email too just more of an introduction email about me and my research.

I also emailed Dr Sylvia Anne Mackie who is the LAS Research Communication Advisor / Convener COM80001 GC-RESIM, at Swinburne’s Office of Student Engagement.

I heard back from Sylvia this morning, who informed me of the following:

quote,

 “Hi Lee,

 In relation to formatting, Appendix 1 in the Statement of Practice Candidature Handbook gives a guide to Swinburne’s preferred structure and format of the thesis (pages 46-48). It’s in the Research Intranet (log in with your staff ID, not your student number):

 https://www.swinburne.edu.au/media/intranet/research/docs/grad-studies-pdfs/SoP-Candidature-Handbook-November-2018.pdf

 If you’re considering the thesis by publication, you should check through p. 47 in detail and then discuss it with your supervisor.

 Swinburne’s Research Bank has samples of completed theses: access the repository via the link, and browse by publication type.”

[sudheervanguri]

Lupin Limited WALK-IN Interview at Hyderabad Lupin Limited, a renowned name in the pharmaceutical industry, is conducting a WALK-IN interview in Hyderabad. This event offers numerous opportunities for experienced professionals in Production, Engineering, Quality Assurance (QA), and Quality Control (QC). If you have a background in B.Sc., M.Sc., B. Tech, Diploma, or B. Pharm, this is your chance to join a top MNC company and advance your career. Lupin Limited Walk-In Interview Details Date & Time: 30th June 2024, 10:00 AM - 4:00 PM Venue: Hotel Kinara Grand, H. NO. 1-57/90, Beside My Home Jewels, Near Madinaguda Bus-Stop, Madinaguda, Hyderabad Available Positions Production (API) Location: Mandideep Site (Bhopal), MP Designations: EA (Associate), EO (Jr. Officer), E1 (Officer), E2 (Executive) Qualification: B.Sc./M.Sc. (Chemistry), Diploma/B.E. (Chemical) Experience: 2-10 years Job Description: Operate equipment like reactors, Sparkler Filter, Candle Filters, Centrifuge, Dryers as per SOP. Experience with SCADA upgradation, CSV, and equipment qualification is preferred. Engineering - Instrumentation (OSD/API) Location: Mandideep Site (Bhopal), MP Designations: EA (Associate), EO (Jr. Officer), E1 (Officer), E2 (Executive) Qualification: Diploma/B.E./B. Tech (Instrumentation) Experience: 2-10 years Job Description: Experience with PLC and SCADA programming, SQL database software, field instrumentation, troubleshooting, and SCADA system upgrades. Quality Control (API/FML) Location: Mandideep Site (Bhopal), MP Designations: Sr. Officer/Officer Qualification: B.Sc./M.Sc. (Chemistry), B. Pharm/M. Pharm Experience: 2-10 years Job Description: Hands-on experience with HPLC, GC, KF, IR, UV, lab instruments, and troubleshooting. Familiarity with QC software like Tiamo 3.0, LIMS, QAMS, SAP, Chromeleon 7.3, and knowledge of cGMP and DI (ALCO+). Quality Assurance (API/FML) Location: Mandideep Site (Bhopal), MP Designations: Sr. Officer/Officer Qualification: B.Sc./M.Sc. (Chemistry), B. Pharm/M. Pharm Experience: 2-10 years Job Description: Review of BPR, batch cleaning records, test data sheets, sampling of API finished goods, preparation of APQR, handling QMS documents, and preparing responses to customer queries and questionnaires. Required Documents to attend Lupin Limited Hyderabad walk in interview Candidates attending the interview should bring the following documents: Updated CV Recent photograph Academic certificates (10th, 12th, Graduation, PG) Offer and appointment letters Current CTC breakup and last three months' salary slips Relieving letter from previous employers PAN card and Aadhaar card (self-attested copies) [caption id="attachment_58299" align="aligncenter" width="930"] Lupin Limited Recruitment Notification[/caption] Important Information Minimum 60% in the highest education is a must for candidates with less than 5 years of experience. Candidates who have given an interview within the last 6 months are not eligible to apply. Lupin Limited does not charge any fees or accept any security deposits from job seekers.