#RLD supplier

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RLD Supplier | Clinical Trial Supply | RLD Sourcing

Reference Listed Drug Sourcing is not as easy as it sounds. Therefore, it is extremely necessary to have a reliable source who understands all your needs as well as the market. As a trusted/reliable RLD supplier, we legally supply Reference Listed Drugs/ Innovator Drugs/ Comparator Drugs for bioequivalence study / clinical trials from the US, EU, UK, Canada, Australia, Brazil, etc. Kindly Call/WhatsApp: +91 8130290915 or dial TOLL-FREE: 1800-889-1064 to procure your Innovator or RLD supply. Having tie-ups with different innovative companies, IKRIS Pharma Network (IPN) can be completely reliable when it comes to sourcing Reference Listed Drugs (RLDs).

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NewLife Medicals: Your Trusted Global Clinical Research Organization

Riding on the cutting edge of medical science and clinical trials, NewLife Medicals is your reliable partner for all pharmaceutical needs. Bathing in expertise, authority, and trust, our ambitious goal is to reshape the future of healthcare.

But why should you trust NewLife Medicals?

NewLife Medicals: Active Pharmaceutical Ingredient Manufacturers

Active pharmaceutical ingredients (APIs) are the heart of any medicine, responsible for its therapeutic effects. At NewLife Medicals, we are more than just API manufacturers. Quality, affordability, and ultra-precision define our API manufacturing. We utilize state-of-the-art technology and rigorous quality checks to ensure the synthesis of high-quality APIs.

Got an unusual API request? As hard-to-source drugs and limited distribution drugs suppliers, we welcome the challenge!

Clinical Research Organization: NewLife Medicals

Clinical trials form the backbone of drug development – but they can be complex and costly. Simplify and economize your clinical testing experience with our unparalleled clinical research organization. Our seasoned team of research professionals are committed to delivering high-quality, timely, and ethically sound clinical research.

Why settle for less when you can have the best?

Global Innovator Drugs Supplier and Biosimilar Supplier

As an innovator drugs supplier, NewLife Medicals is committed to bringing new, pioneering treatments to the market. Our extensive portfolio of innovator drugs and biosimilar infusions stands as a testament to our pioneering spirit and relentless dedication to progress.

Ever heard of orphan drugs or REMS access? We supply these too!

Finished Dosage Formulations Suppliers

We take our role as finished dosage formulations suppliers seriously. Our manufacturing process leverages the highest industry standards, ensuring consistency and efficacy with every dose. Whether it's tablets, capsules, or syrups, we have your needs covered.

Are you seeking a reliable reference listed drug provider? Look no further!

Ancillary Clinical Supplies and Hospital Lines Supplier

Besides pharmaceuticals, our inventory comprises ancillary clinical supplies and premium hospital lines. These medical accessories and equipment promise to simplify your caregiving experience, improving efficiency and compliance.

Are you with us yet?

Your Trusted Partner in Pharmaceutical Supply Chain

Whether it's comparator sourcing for clinical trials, pharma raw material suppliers, patient supply, or specialty sourcing, NewLife Medicals has got you covered. Our integrated supply chain caters to all your pharmaceutical needs while maintaining the highest quality standards.

Trust in the expertise and authority of NewLife Medicals for all your medical needs. Together, let's make a healthier world!

Meta description: Explore NewLife Medicals – your trusted global clinical research organization, pharmaceutical supplier, and healthcare partner. Dive into our wide range of services today.

[trodelvy]

Trodelvy Injection: A Game-Changer in Cancer Care

Trodelvy contains the active pharmaceutical ingredients sacituzumab govitecan. The medicine is used for the treatment of patients with triple-negative breast cancer (TNBC), HR+/HER2- metastatic breast cancer, and advanced bladder cancer. If you are searching for a genuine Trodelvy supplier from India, then Indian Pharma Network (IPN) can be your most reliable source/platform. IPN is WHO GDP & ISO 9001 2015 Certified Trodelvy Supplier, Wholesaler, Importer, and Exporter from India. Trodelvy which is Manufactured by Gilead Sciences, Inc, is available in a strength of 180 mg/mL. Trodelvy 180 mg is supplied for Tenders/ exports/ imports/ Named patient program/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples for Clinical trials. Indian Pharma Network is the legitimate source of Trodelvy (sacituzumab govitecan-hziy) for injection, all the customers can get in touch with us to buy/order/procure this pharmaceutical product in approved quantity.

Buy Trodelvy 180 mg Injection at Lowest Price from India

Trodelvy 180 mg for injection is designed to carry cancer-fighting drug to cells that have Trop-2 proteins. Certain tumor cells have high Trop-2 proteins. The medicine trodelvy 180 mg injection is approved for 3 different types of cancer:

Advanced Bladder Cancer

HR+/HER2- Metastatic Breast Cancer

Metastatic Triple Negative Breast cancer Trodelvy injection 180 mg is a type of antibody-drug conjugate (ADC) treatment that is designed to work differently than traditional chemotherapy. It is designed to deliver promising anticancer drug directly into cells with Trop-2 proteins.

Buy Trodelvy in India I Sacituzumab Govitecan 180 MG Vial

Trodelvy (sacituzumab govitecan) is a type of medicinal product known as antibody-drug conjugate, or ADC for short. Unlike typical (traditional) chemotherapy, ADCs consist of three parts: an antibody, an anticancer medicine, and a linker. If you want to buy trodelvy in India for triple-negative breast cancer, HR+/HER2- metastatic breast cancer, and advanced bladder cancer, then Indian Pharma Network (IPN) can be your one-stop solution.

We are famed and esteemed in the pharmaceutical industry for our best quality service, vast industry experience, market credentials, and timely delivery. Our all the tie-ups and sourcing from the reputed brands allow us to offer the best price for Trodelvy 180 mg vial. Trodelvy (sacituzumab govitecan 180 mg vial) is an intravenous (IV) infusion (10mg/kg). Proposed doses are administered once weekly for two weeks (Day 1 and 8) of 21-day treatment cycles. Each treatment cycle is 21 days (3 weeks).

Sacituzumab Govitecan- Trodelvy Price for 180 MG Vial in India

Trodelvy is made of two different drugs joined together: a monoclonal antibody drug (which attaches to Trop -2 receptors, present on the outside of some cancer cells, and a chemotherapy drug (which stops all cells including unhealthy cells from growing and dividing). The monoclonal antibody drug attaches to the unhealthy cells and then releases the chemotherapy medicine directly into the cell. All pharmaceutical products – comparator drugs, adjunctive therapies, RLDs, co-meds and rescue meds, and Exports/Imports drugs – are transported in standard temperature-controlled conditions with active monitoring in order to ensure the integrity of products. Contact us today to get/buy your hard-to-access prescription medicine at the lowest price from India.

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Strategies for Efficient Sourcing and Procurement of RLDs from Belgium

Introduction:

In the dynamic landscape of pharmaceuticals, sourcing and procuring Reference Listed Drugs (RLDs) from Belgium stand as crucial endeavors for companies seeking innovation and quality. Belgium's pharmaceutical industry is renowned for its excellence and cutting-edge research, making it a prime destination for sourcing RLDs. At the forefront of this process is Invimeds, a trusted partner facilitating efficient procurement of RLDs from Belgium. 

In this blog, we will explore key strategies for efficiently sourcing and procuring RLDs from Belgium, leveraging the country's expertise and infrastructure, with a focus on the pivotal role played by Invimeds in facilitating this process.

Belgium's Pharmaceutical Sector

Belgium plays a pivotal role in driving pharmaceutical innovation on a global scale. It stands out as a prominent leader in the industry, boasting nearly 30,000 skilled professionals and contributing over 10% of the country's total exports. The Belgian government and pharmaceutical sector are deeply committed to furthering industry growth, with substantial investments focused on innovation and research and development (R&D). 

Annually, the pharmaceutical industry channels more than €1.5 billion into R&D efforts, representing a significant portion of private investment in Belgium, exceeding the European average by double. These investments support the extensive research required to identify and develop new drugs, establish their safety and efficacy profiles, and obtain regulatory approval. This steadfast commitment to innovation underscores Belgium's position as a key player in shaping the future of the pharmaceutical landscape.

InviMeds as a RLD Supplier

Belgium's pharmaceutical sector is characterized by a strong emphasis on research and development, coupled with robust regulatory frameworks. Invimeds, a key player in the pharmaceutical industry, strategically partners with reputable firms in Belgium.

Through global collaborations with certified suppliers from the USA, EU, Korea, Latam, and Japan, Invimeds ensures a seamless supply chain for reference-listed drugs (RLDs) worldwide. Upholding EU-GDP standards, Invimeds prioritizes transparent communication and strategic planning to swiftly address any distribution challenges. 

These partnerships grant Invimeds access to a diverse portfolio of high-quality RLDs, ensuring availability across various therapeutic areas while adhering to stringent quality and regulatory standards. Invimeds ensures the integrity of the procurement process. Our services include single and multiple batch sourcing, tailored to specific quantities and expiration dates.

Ensuring Authenticity and Integrity of RLDs

Maintaining impeccable quality standards is paramount in pharmaceutical procurement, particularly when dealing with Reference Listed Drugs (RLDs). Invimeds as an RLD supplier in Belgium, places the utmost emphasis on quality assurance throughout the procurement journey. 

Employing meticulous selection criteria and rigorous quality control measures, Invimeds ensures that RLDs acquired from Belgium adhere to the most stringent standards of safety, efficacy, and authenticity. This unwavering commitment instills confidence in pharmaceutical companies regarding the reliability and integrity of the RLDs sourced through Invimeds.

Invimeds goes above and beyond to guarantee the authenticity and quality of the RLDs it procures. We offer comprehensive certifications, encompassing Certificates of Analysis (COA), Batch Reports, and Certificate of Origin (COO), showcasing adherence to WHO EU guidelines, FDA, and EMA regulations. By adhering to these regulatory benchmarks and providing transparent documentation, Invimeds reaffirms its dedication to delivering only the highest-quality RLDs to our valued clients.

InviMeds Transportation Excellence

At Invimeds, we specialize in logistics and shipping, ensuring the safe and efficient transportation of pharmaceuticals. Committed to product safety, we strictly adhere to global regulations and offer comprehensive licensing support for regulatory compliance. Our state-of-the-art warehousing facilities prioritize medication safety with advanced temperature controls, robust security measures, and 24/7 monitoring through data loggers. 

From inventory management to secure handling, we emphasize efficiency while maintaining stringent quality standards. Additionally, we establish thorough Quality Agreements and Service Level Commitments to promote transparency and uphold industry standards.

Ensuring Prompt Delivery and Reliable Service

At Invimeds, timeliness is paramount. We prioritize efficiency from procurement to delivery, ensuring prompt processing and dispatch of orders. Our dedicated logistics team coordinates with clients every step of the way, guaranteeing seamless communication and timely updates. Recognizing the criticality of timely delivery in the pharmaceutical industry, we go the extra mile to meet our client's timelines. Invimeds is committed to excellence in timeliness, ensuring that every aspect of our service exceeds expectations.

Conclusion:

The efficient sourcing of RLD from Belgium requires a multifaceted approach that encompasses leveraging the country's pharmaceutical excellence. Invimeds, with its unwavering commitment to quality and patient care, serves as a trusted partner in this process, facilitating seamless transactions and reliable access to essential medications. 

By collaborating with Invimeds, pharmaceutical companies can navigate the complexities of RLD sourcing and procurement with confidence and efficiency, ultimately advancing their goals in drug development and patient care. If you're seeking a trusted partner for RLD sourcing from Belgium, look no further than Invimeds. Contact us today to embark on a journey of unparalleled reliability and success in pharmaceutical procurement.

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Global Excellence in Delivery Device Testing

Introduction

There is a need for a fully-informed laboratory in combination device validation services. The ideal is a laboratory that understands both the pharmaceutical and medical device requirements; from extractables and leachables, through bioavailability, to dose accuracy and ease of use. A good pre-clinical partner/test facility, such as Medical Engineering Technologies Ltd. (MET, www.met.uk.com) can provide regulatory guidance and Design Validation Testing (DVT) to help assist in getting a product to the marketplace.

The process of generating performance and safety data should be planned to ensure efficient project management and to help reduce costs.

Design Validation Planning

The pre-requisites to developing a design validation programme are:

Competitor submissions review

Design inputs / targeted product performance

European and/or FDA Guidance review

Risk analysis

ISO /EN /ASTM/ ICH/ pharmacopeia standards review

(If this is a first foray into combination devices) A gap analysis of the Quality Managements System (QMS) and production processes and qualifications in place.

A review of existing product standards and Guidance, along with detailed risk analysis, is essential to defining test programmes. This approach ensures that all the necessary testing has been carried out, and can also reduce any unnecessary testing. Additionally, the key performance requirements must be identified in a product review; this includes design inputs and a literature review. To assist you in saving time and money, MET has developed standard study plans for a large range of devices.

These reviews and risk analyses can then be used to develop the test programme and design test protocols.

Developing a Protocol

The testing regimes in a DVT could include:

Assessment of hazards identified in the risk analysis

Bioavailability studies

Biocompatibility studies

Drug / container interaction analysis

Extractables and leachables studies, toxicological risk analysis

Human factors studies

Performance and dose accuracy assessments

Reference Listed Drug (RLD) comparison

Standard / FDA Guidance compliance testing

Gantt charts and a more descriptive plan, provided by your partner laboratory, keep you informed. These plans can include test cost, time requirements, sample numbers, and an indication of whether a test is essential (or just helpful).

MET testing plans shown below use a transdermal patch as an example and give an idea of the types of testing, sample sizes and time requirements that would need to be considered. These tables are not comprehensive.

Transdermal biocompatibility and chemical safety:

Transdermal  performance tests:

Transdermal distribution testing:

Design Validation Testing (DVT)

All planned tests will require agreed test protocols. These are developed by your test facility, with your approval.

The testing stage might be preceded by a Gauge Repeatability and Reliability (GR&R) study, to provide evidence that the test protocol is robust and that there can be confidence in the DVT results.

The use of a laboratory with ISO/IEC 17025 accreditation will ensure that there is a good, fully audited, QMS and that equipment is qualified and calibrated, whilst processes are subjected to internal audits. It is entirely possible that not all the tests will be specifically accredited. As long as these are carried out to an agreed protocol under the ISO/IEC 17025 QMS, there can be confidence in the results.

Reporting

Test reports can be succinct or extensive. For regulatory submissions, a Certificate of Analysis will be too brief whilst as 100 page report will not be helpful.

The report should include at least:

The test protocol (this can be an appendix)

The rationale for analyses included and excluded

Any deviations from test protocol

Details of equipment and technicians

Details of the product/s tested (batches, dates, description, etc…)

Test results

Summary

Summary

When developing a combination device, a pharmaceutical company must decide whether to carry out testing in-house or externally. There is no compulsion for independent testing, as long as a company’s own laboratory is fully equipped, has all the control systems in place, and will act without bias.

The advantages of using an experienced, well informed external laboratory are:

Clear independence

No capital costs

Efficiency of project management, testing and reporting

Good advice from a knowledgeable source.

Things to look for when selecting a laboratory are:

A good QMS and good quality control

Informed and helpful staff

Rapid, accurate responses to queries

Openness of access

A comprehensive range of services, in order to reduce multiple sourcing and adding several companies to your supplier list.

Medical Engineering Technologies (MET) has staff that have developed plans for many projects and a wide variety of devices. These have been successfully implemented within an ISO/IEC 17025 QMS, helping clients achieve a smooth entry into the market (www.met.uk.com).

The post Global Excellence in Delivery Device Testing appeared first on MassDevice.

from MassDevice http://bit.ly/2BW4WyO

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Top Reference Listed Drug (RLD) Supplier in India

Are you seeking for the most simple approach to order reference materials for clinical studies/trials and analytical purposes? Ikris Pharma Network (IPN), the best Reference Listed Drug supplier, can assist in obtaining the necessary samples and related medical product details in a timely and efficient manner. To learn more about our reference products or services, please contact us at 1-800-889-1064 or call or WhatsApp +91 8130290915. Ikris Pharma Network (IPN) provides entire service from sourcing to delivery for all reference products (Reference Listed Drugs - RLDs, Comparator Drugs).

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Top Exporter of API & Intermediates For The Pharmaceutical Industry

The top supplier for API and Intermediates for the pharmaceutical industry. High-quality products, reliable service, and competitive pricing. Contact us now.

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Save valuable time with certificate lab integrations

With EssentiaApp you don’t need to worry about inserting the certificate details, scanning the certificate or trying to find a way to share it with potential customers. It’s all done automatically for you.

Save valuable time with certificate lab integrations

With EssentiaApp you don’t need to worry about inserting the certificate details, scanning the certificate or trying to find a way to share it with potential customers. It’s all done automatically for you.

Real-time inventory management

Real Time Inventory management from any device: computer, tablet and smartphone. This helps you to control your entire inventory from any place, any digital device all across the world.

Manage your business on the go

Whether you are traveling to an exhibition or visiting customers, with EssentiaApp you can search your inventory, issue & email a price quotation or create an invoice on the spot.

Never stop marketing your inventory

EssentiaApp automatically syncs your inventory with all leading diamond marketplaces, letting you focus on other aspects of your business while actively marketing your inventory.

Stay on top of your business with documentation management

EssentiaApp lets you issue, print and share documents with your company letter head in just a few clicks. All documents are saved in your history, which means you can always view, edit or re-print these anytime and from anywhere.

About Accadia

Accadia Software Technologies Limited was established in 2003 by AdiShva, and AdiEilon with the specific goal of providing management solutions for the diamond, colored gemstone and jewelry industries.

Accadia gained over 20 years experience in the diamond software industry and is currently serving the largest customer base for diamond management software in the world with offices in Ramat Gan (ISR), Antwerp (BEL) and representatives in New York (USA), London (UK) and Johannesburg (SA).

Features:

•             Insert data into the inventory list either manually, or via Excel

•             Retrieve certificates data and PDFs directly from labs

•             Online status and location management of single stones

•             Export filtered stock list to Excel and PDF in various formats

•             Automatic upload stock to all major ecommerce platforms

•             Upload and publish your diamonds inventory in your website

•             Create, and manage customers’ accounts

•             Issue price quotations, memos and sale invoices to customers

•             Create and manage suppliers (vendors) accounts

•             Issue consignments and purchase notes from vendors

•             Basic financial management of accounts receivable (coming soon)

•             Basic financial management of accounts payable (coming soon)

•             Optimized for teams of following number of concurrent users

For more details on our products and services, please feel free to visit us at diamond management, diamond system & diamond software

[invimedsblog]

Streamlining Supply Chains: How Invimeds Facilitates RLD Procurement from Germany for Pharma Industry

In the fast-paced world of pharmaceuticals, efficiency, and reliability in the procurement of Reference Listed Drugs (RLDs) are crucial. Invimeds emerges as a trusted ally for the industry, particularly in Germany, for pharmaceutical manufacturing. Let's explore how Invimeds simplifies the RLD procurement process, ensuring compliance, quality, and seamless operations.

Certified Partnerships: Invimeds operates with a validated network of suppliers, adhering to stringent EU-GDP guidelines. This ensures that every step of the procurement process meets regulatory standards, safeguarding the authenticity and quality of RLD sourcing from Germany.

Regulatory Compliance: Navigating the complex regulatory landscape is simplified with Invimeds. Our team of experts ensures adherence to all necessary permits and approvals, guaranteeing legal importation and distribution of controlled substances. Transparency is paramount, with comprehensive documentation, including Certificates of Analysis (COA), Batch Reports, and Certificates of Origin (COO), provided for every transaction.

Temperature Monitoring: Maintaining the integrity of RLDs during transit is paramount for pharmaceutical companies, and Invimeds takes this responsibility seriously. We employ advanced data loggers to monitor temperature fluctuations in real time, ensuring that medications remain within the specified temperature range throughout transportation. 

This meticulous temperature control, coupled with our state-of-the-art warehouse hubs across Europe, the USA, South Korea, and Australia, safeguards the efficacy of RLDs. Pharmaceutical companies can rest assured knowing that their products are in good hands with Invimeds, providing them confidence in their supply chain management.

Tailored Solutions: Every pharmaceutical company has unique needs and challenges. Invimeds understands this diversity and offers customized solutions for RLD procurement. Whether it's sourcing specific RLDs, managing bulk orders, or addressing regulatory complexities, our personalized assistance guides clients through the procurement process with ease.

In conclusion, Invimeds is dedicated to revolutionizing supply chain management with its cutting-edge RLD solutions. By placing a strong emphasis on quality, compliance, and efficiency, Invimeds empowers pharmaceutical companies to streamline their operations and deliver life-saving medications to patients around the globe. 

If you're in search of an RLD supplier in Germany, look no further than Invimeds. With our extensive network in Germany, we specialize in procuring RLDs for pharmaceutical research, development, and trials. Our commitment to excellence ensures that you receive reliable and high-quality RLDs tailored to your specific needs. Reach out to Invimeds today and experience the difference in supply chain optimization.

[ikrispharmaa]

Ikris Pharma Network | International pharmaceutical wholesaler

Ikris Pharma Network founded in 2014 and is based in Noida, India. We are one of the most reliable pharmaceutical companies for generic and branded medication (AstraZeneca, Pfizer, Sun Pharma etc.) supplies globally, making it a key player in the industry.

Ikris Pharma Network has a vast and wide range of 5000+ generic and branded drugs’ distribution services globally and is one of the top notch generic medicine suppliers. As a branded and generic medicine supplier, we specifically deal in all types of medicines i.e. tablet, capsules, liquid, topical, suppositories, drops, inhalers, injections, implants or patches etc.

Ikris Pharma Network offers to its clients (hospitals, dispensaries, patients, pharmacies) up to date pricing and inventory levels, order status. With Ikris Pharma Network, clients have access to direct reach to 5,000+ branded & generic medicine & health care products, and their pricing related deets and Simplified, intuitive, branded & generic drug ordering. 

In the industry of healthcare, we acknowledge that the one size usually does not fit all. And whether we're delivering pharmaceuticals or biopharmaceuticals, such as vaccines, we're completely aware that our patients depend on prompt as well as punctual delivery of their pharmaceutical products. We understand that our patients place trust in us to deliver for them. With Ikris Pharma Network, you can count on us to deliver for you.

Our efficiently optimised transportation and logistics services, large-scale global network, absolutely strict adherence to national and international compliance, and topmost or supreme end-to-end visibility allows/enables our clients’ supply chains with agility, balance, and speed to industry. 

Our experienced team is working relentlessly around the clock to ensure your precious and often life-saving shipments get to where they need to be - securely, at the appropriate and standard temperature, and on time.

From branded to Indian generic medicines, from RLD to Named Patient Program, Ikris Pharma Network delivers reliability for each customer across the industry. Have peace of mind in order to know that we have been delivering reliable solutions for our life science customers at the global level.

With proficient professionals, sophisticated processes, and impeccable reliability, it is our aspiration and liability to keep up to ensure our clients’ supply chains and businesses both succeed and thrive. 

We have assisted more than 50,000+ patients to date. We offer Validated and Customized solutions for cold chain products including vaccines We have Exported Indian Generic drugs to over 150+ nations including Romania, Brazil, China, South Africa, Italy, UK, Russia, Poland, Mexico, Latvia, etc.

[ikrispharmaa]

Ikris Pharma Network founded in 2014 and is based in Noida, India. We are one of the most reliable pharmaceutical companies for generic and branded medication (AstraZeneca, Pfizer, Sun Pharma etc.) supplies globally, making it a key player in the industry.

Ikris Pharma Network has a vast and wide range of 5000+ generic and branded drugs’ distribution services globally and is one of the top notch generic medicine suppliers. As a branded and generic medicine supplier, we specifically deal in all types of medicines i.e. tablet, capsules, liquid, topical, suppositories, drops, inhalers, injections, implants or patches etc.

Ikris Pharma Network offers to its clients (hospitals, dispensaries, patients, pharmacies) up to date pricing and inventory levels, order status. With Ikris Pharma Network, clients have access to direct reach to 5,000+ branded & generic medicine & health care products, and their pricing related deets and Simplified, intuitive, branded & generic drug ordering. 

In the industry of healthcare, we acknowledge that the one size usually does not fit all. And whether we're delivering pharmaceuticals or biopharmaceuticals, such as vaccines, we're completely aware that our patients depend on prompt as well as punctual delivery of their pharmaceutical products. We understand that our patients place trust in us to deliver for them. With Ikris Pharma Network, you can count on us to deliver for you.

Our efficiently optimised transportation and logistics services, large-scale global network, absolutely strict adherence to national and international compliance, and topmost or supreme end-to-end visibility allows/enables our clients’ supply chains with agility, balance, and speed to industry. 

Our experienced team is working relentlessly around the clock to ensure your precious and often life-saving shipments get to where they need to be - securely, at the appropriate and standard temperature, and on time.

From branded to Indian generic medicines, from RLD to Named Patient Program, Ikris Pharma Network delivers reliability for each customer across the industry. Have peace of mind in order to know that we have been delivering reliable solutions for our life science customers at the global level.

With proficient professionals, sophisticated processes, and impeccable reliability, it is our aspiration and liability to keep up to ensure our clients’ supply chains and businesses both succeed and thrive. 

We have assisted more than 50,000+ patients to date. We offer Validated and Customized solutions for cold chain products including vaccines We have Exported Indian Generic drugs to over 150+ nations including Romania, Brazil, China, South Africa, Italy, UK, Russia, Poland, Mexico, Latvia, etc.

[ikrispharmaa]

Access to Vital Medications: Role of Ikris Pharma in Clinical Supply Chain

In the intricate world of pharmaceuticals, Ikris Pharma stands out as a leading player in the realm of reference-listed drug suppliers and clinical supply chain management. Let's understand what sets us apart and how it plays a crucial role in ensuring the availability of essential medications for clinical trials and healthcare settings.

Reference Listed Drugs & Its Sourcing: Reference-listed drugs serve as the standard against which generic drugs are compared for safety and efficacy. Ikris Pharma excels in sourcing these essential medications, ensuring that clinical trials have access to the necessary reference drugs for accurate evaluation. By maintaining a robust network of trusted suppliers and adhering to stringent quality standards, the company facilitates seamless access to reference-listed drugs (RLDs) for research and development purposes.

Clinical Supply Chain Management: Managing the clinical supply chain is a complex endeavor that needs meticulous planning and execution. We specialize in navigating this complex process, offering comprehensive solutions for the procurement, storage, and distribution of therapeutic drugs for clinical trials. With a focus on efficiency and reliability, we streamline the supply chain, ensuring that investigational drugs reach clinical trial sites in a timely and compliant manner.

Comparator Drug Sourcing: Comparator drugs play a crucial role in clinical trials by serving as a reference for evaluating the safety and efficacy of investigational drugs. Ikris is a trusted partner in sourcing comparator drugs, leveraging its extensive network and expertise to procure these essential medications. Whether sourcing commercially available products or coordinating with manufacturers for custom formulations, we ensure that clinical trials have access to the comparator drugs required for accurate and meaningful research outcomes.

Ensuring Compliance and Quality: In the realm of clinical research, compliance and quality are foremost. With a focus on sourcing all the essential medications from reputable suppliers and manufacturers, Ikris Pharma Network ensures the integrity and authenticity of every product it delivers. The company adheres to stringent regulatory standards and industry best practices to ensure the integrity and reliability of the medicines supplied. Through rigorous quality assurance processes and adherence to Good Distribution Practices (GDP), Ikris upholds the highest standards of excellence in every aspect of its operations.

Driving Innovation and Advancement: As clinical research continues to evolve, the demand for reliable and efficient supply chain solutions grows. As a leading reference-listed drug supplier, Ikris Pharma remains at the forefront of innovation, continually seeking new ways to enhance its services and support the advancement of medical research. By providing seamless access to reference-listed drugs, managing the clinical supply chain with precision, and sourcing comparator drugs with expertise, the firm plays a valuable role in the progress of the field of clinical research.

In conclusion, Ikris Pharma stands as a trusted partner in the clinical supply chain. We offer unparalleled expertise in sourcing reference-listed drugs and comparator drugs for clinical trials. With a commitment to compliance, quality, and innovation, we remain dedicated to supporting the advancement of medical research and improving patient outcomes.

Feel free to reach out to us today via email at info@ikrispharmanetwork.com to learn more about our services or if you have any queries. We're here to help.