techsolcorpmarketing-blog

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Medical Information Portal | MedInquirer Self-Service Portal

Medinquirer selfservice portal

Interactive channel to provide accurate medical information for your customers

MedInquirer Self-Service Portal Lets HCPs, Non-HCPs and Physicians to Readily Socialize with Pharma and Get Precise online Medical Information Concerning the Provider's products.

Key Features

Has Got Visitor Qualification for HCPs & Non-HCPs Could be tailored to possess the Pharma firm brand feel & look Lets screen of Configurable Online MI / AE & PC Data Capture Forms info and scientific material provisioned to be accessible on portal could be searched and obtained Lets display of additional articles like Therapeutic locations, Products and also other applications including PAP, Clinical Trials, etc.. Online Requests & AE/PC Submissions mechanically creates a situation in MedInquirer May Also be integrated readily with other Medical Information Systems Consists of distinct accounts for tracking page visits, query admissions and articles utilization Supports Client Online conversation with MI staff Very reactive and also be obtained on notebooks, tablets and Cellular telephones

Solution Benefits

HCPs & Non-HCPs can easily submit an internet Medical Information Request or report an Adverse Event or Merchandise Complaint for a Particular merchandise They can easily Learn More about the business products by hunting and obtaining provisioned FAQs and other Content Right on the portal site

Sponsors

Could leverage a different digital station to enable their clients through LIVE chat discussion and from providing accurate medical advice Build more information regarding their product functionality and customer needs together with all the portal site reports & dashboards.

Read more about .....medical information portal

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Veeva CRM | CRM integration | GxP Compliance | Medical Information

MedInquirer Integration - To facilitate seamless stakeholder collaboration and lean business processes, MedInquirer is designed to enable bi-directional integration paths using validated RESTful APIs. 

All upstream integrations are established with certified APIs of MedInquirer On successful receipt of external data, a new MI Case is directly created within MedInquirer Since the integration is bi-directional, an acknowledgment alert is auto-sent with the status of case creation.

All Adverse Events captured in MedInquirer can be directly transmitted to E2B compliant Drug Safety systems for regulatory reporting PCs in MedInquirer can be transmitted as XML files which can be later processed directly into PQC systems for further analysis & review.

For more information please visit here:  https://www.techsolcorp.com/medinquirer-integration/

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Veeva CRM | CRM integration | GxP Compliance | Medical Information

MedInquirer Integration - To facilitate seamless stakeholder collaboration and lean business processes, MedInquirer is designed to enable bi-directional integration paths using validated RESTful APIs. 

Incoming medical inquiries received by the sales team in Veeva ® CRM can be readily made available in MedInquirer for speedy response fulfillment MedInquirer Vault.

MedComm integration Allows the approved medical information content stored in the Vault to be readily available in MedInquirer for the preparation of response packages. MedInquirer cloud is hosted on a GxP validated AWS Cloud platform. It has security and quality certifications such as ISO 9001, ISO 27001, ISO 27017, and ISO 27018 and the platform is SOC-2 compliant. 

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Signal Management in Pharmacovigilance | Drug Safety Software

Drug Safety Software: Techsol CaseIRT is an advanced solution for Intake, Receipt, and Triaging of Adverse Events and Product Complaints. It works as a staging tool to hold data before it can be transferred to appropriate systems.

Pharmaceutical organizations and CRO or KPO organizations receive a load of inquiries reporting adverse events and product complaints on a regular basis. All the adverse events and product complaints must be reported in a timely manner, but it is also essential to qualify events before reporting. The challenges pharma companies are facing today include:

Capturing information from various sources into one single platform.

Ensuring the validity of each adverse event and product complaint about reporting in a timely manner. Adhere to regulatory compliance across departments, business unit, and geographies. Techsol CaseIRT is an advanced solution for Intake, Receipt, and Triaging of Adverse Events (AEs) and Product complaints (PCs). It works as a staging tool to hold data before it can be transferred to appropriate systems. CaseIRT enables companies to harmonize their data receipt, assessment and tracking globally using one platform, leading to improved regulatory compliance and overall process efficiency. It helps companies to:

Maintain a single platform for capturing inquiries from multiple sources including affiliates, partners, medical information Call Centers, suppliers, and third-party systems. Validate the authenticity and accuracy of each case to be marked for reporting by using in-built validation rules and duplicate search. It uses an integrated rule-based Retrospective Quality Assurance process.

Integrate with various systems to ensure timely reporting of adverse events and product compliant to maintain adherence to the various regulatory compliance. It also provides a global and local Inbox to manage all the incoming data via various channels.

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AccelClinical | Clinical data management | EDC systems for clinical trials

AccelClinical is a fully-managed, cloud-based integrated clinical data management solution offered by Techsol using Oracle Clinical, Oracle Remote Data Capture (RDC) and Oracle Thesaurus Management System (TMS) applications.

Using AccelClinical, emerging biopharma companies, device manufacturers, and service providers can easily manage Case Report Form (CRF) design, study data collection, discrepancy management, medical coding and study data reporting across Phase 1 to Phase IV clinical trials.

Our unified solution allows customers to conduct both paper-based and electronic data capture (EDC) clinical trials seamlessly with built-in edit checks for facilitating faster data cleansing and generating high-quality data sets for statistical analysis.

For more information please visit here: https://www.techsolcorp.com/accelclinical/

[techsolcorpmarketing-blog]

Signal Management in Pharmacovigilance | Drug Safety Software

Drug Safety Software: Techsol CaseIRT is an advanced solution for Intake, Receipt, and Triaging of Adverse Events and Product Complaints. It works as a staging tool to hold data before it can be transferred to appropriate systems.

Pharmaceutical organizations and CRO or KPO organizations receive a load of inquiries reporting adverse events and product complaints on a regular basis. All the adverse events and product complaints must be reported in a timely manner, but it is also essential to qualify events before reporting.

For more information please visit here: https://www.techsolcorp.com/safety-and-signal-management/

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Clinical Trial Disclosure | EDC Systems for Clinical Trials

Clinical trial submission software: TrialMaster is an intuitive electronic data capture system that helps organizations achieve faster trial completion. It is designed to automate the submission of clinical trials & their results data to EudraCT and other registries. To know more about EDC in clinical trials, visit us.

For more information please visit here: https://www.techsolcorp.com/clinical-trialdisclosure/

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TrialMaster Solution | Electronic data capture in clinical trials

TrialMaster is an intuitive electronic data capture system that helps organizations achieve faster trial completion, improved efficiency, and reduced costs. Techsol, in partnership with Omnicomm Systems, provides its clients the TrialMaster solution. TrialMaster is an intuitive electronic data capture system that helps organizations achieve faster trial completion, improved efficiency, and reduced costs.

For more information please visit here: https://www.techsolcorp.com/trialmaster/

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Clinical Trial Disclosure | EDC Systems for Clinical Trials

Clinical trial submission software: TrialMaster is an intuitive electronic data capture system that helps organizations achieve faster trial completion. It is designed to automate the submission of clinical trials & their results data to EudraCT and other registries. To know more about EDC in clinical trials.

TrialDisclose is a software product that is designed to automate the submission of clinical trials and their results data to clinicaltrials.gov, EudraCT and other registries. It enables compliance, data consistency and re-use of trial disclosure data across multiple registries.

For more information please visit here: https://www.techsolcorp.com/clinical-trialdisclosure/

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Medical Information management | Clinical Trial Software

TechSolCorp is a single platform for the medical industry needs like clinical development, life sciences solutions, business optimization and more.

For more information please visit here: https://www.techsolcorp.com/

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Medical Information management | Clinical Trial Software

TechSolCorp is a single platform for the medical industry needs like clinical development, life sciences solutions, business optimization and more.

For more information please visit here: https://www.techsolcorp.com/

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TrialOne Solution | Electronic Data Capture - Techsol

At Techsol, we offer fully-managed regulatory compliant cloud hosting for Omnicomm TrialOne solution. We use accelerators to deliver implementation and validation services to all our clients.

For more information please visit here: https://www.techsolcorp.com/trialone/

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Medical Information management | Clinical Trial Software

TechSolCorp is a single platform for the medical industry needs like clinical development, life sciences solutions, business optimization and more.

For more information please visit here: https://www.techsolcorp.com/

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Medical Information management | Clinical Trial Software

TechSolCorp is the single platform for the medical industry needs like clinical development, life sciences solutions, business optimization and more. Techsol provides complete support for your early phase trial automation requirements. We offer fully-managed regulatory compliant cloud hosting for Omnicom TrialOne solution. We use accelerators to deliver implementation and validation services to all our clients.

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Clinical TrialDisclose

TrialDisclose is a software product that is designed to automate the submission of clinical trials and their results data to clinicaltrials.gov, EudraCT and other registries. It enables compliance, data consistency and re-use of trial disclosure data across multiple registries.

Clinical Trial Disclose is a cloud based platform for comprehensive and compliant global clinical trial disclosure, helping regulatory affairs professionals to efficiently plan and execute their disclosure activities:

Supports the end to end process of data collection, review, registry specific validations and generating requisite electronic files for upload to the registry.

Supports Compliance with Global Serialization & Pedigree Regulatory Mandates.

Completely eliminates error-prone manual methods with automated processes and content re-use to dramatically improve productivity and accuracy.

Enables you to meet evolving changing regulatory disclosure requirements with USA, EU and other global agencies.

Enables unsurpassed efficiency, consistency and predictability.

Remain fully compliant with current and evolving clinical trial disclosure regulations.

Ready to deploy integration adapters with source data systems like Electronic data capture, CTMS, SAS data sets and spreadsheets.

How it is Delivered:

Our professional services team consists of domain experts who possess full knowledge of clinical trial disclosure requirements related to FDA, EudraCT shall help manage the overall TrialDisclose solution deployment activities. Our services include:

Solution design activities including business/functional requirement analysis, solution strategy, solution design.

System integration services using accelerators to deliver implementation, validation, upgrade, project management, data/systems migration, end user training.

Fully managed regulatory compliant cloud hosting.

Analysis of source systems, implement and build custom adapters to automate source data import in to Trial Disclose solution.

Remote service desk and application support.

99.9% availability

24/7Service Desk

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Techsol’s

MedInquirer is a next generation, comprehensive, end to end medical information management system that will optimize global compliance, customer satisfaction.

MedInquirer value:

Best in class regulatory compliant platform

24X7 technical supportRobust global service delivery

Continuous product innovationLong term commitment to your success

MedInquirer enables companies achieve:

Optimized patient careGreater process efficiencies

Optimized global complianceMeasurable value and insights

Outstanding overall consumer satisfaction

MedInquirer Benefits:

Rapid and high quality inquiry management – all types MI, AE and PCEffective and easy provisioning of medical information. Simplified and efficient content management

Conduct global and local affiliate inquiry management that scales easily to millions of inquiries

Improve quality, compliance and efficiency through safety and product complaint management integration and automation

Provide Measurable Insights by providing robust reports and simplified analytics

Mobile app to enable simplified inquiry capture

Robust web based zero footprint integrated platform

Complimented by Techsol’s continuous innovation, commitment and 24X7 technical support

Available on Techsol Life Sciences Vertical Cloud in SaaS model and for perpetual subscription to be hosted at your cloud infrastructure

Selective customers can partner in design and innovation through our Strategic Development Partner (SDP) program

MedInquirer feature/functionality overview:

Multichannel  intake of medical information inquiries, AEs and product complaints via multiple company e-Mailboxes, voice mail, Web portal, mobile app and CRM applications

Highly configurable and intuitive user interface that can be standardized across the channels to ensure consistent data intake

Inbuilt Computer Telephony Integration module allows faster capture of information and quickly retrieve customer details

Linking of related inquiries and responses

Easy linking of respective MSL/sales rep to the enquiry.Zero foot print platform accessible on all web browsers

Configurable and intuitive formsValidated adapters that allows two way integrating with Drug Safety Systems and Product Complaint systems

Choice of manual or automated transmissions to downstream systems

Standards based out-of-the-box E2B/HL7 validated two way integration adapter with leading industry Drug Safety Databases

Ready connectors with industry leading Product Complaint Management SystemsIn-built validation rules and duplicate search

Quality control gates at various work flow stages. Integrated rule based Retrospective Quality Assurance process

Global and local Inbox to manage all the incoming data via various channels

Integrated reporting and Business Intelligence capabilities. Ready to use various project management and data listings reports

Fully compliant with FDA 21 CFR Part 11 regulations and provides comprehensive audit trail capabilities for all the changes

Highly configurable and zero footprint web based platformTechsol Validation and Implementation ServicesMedInquirer platform is complimented with our expert professional and validation services to enable a full solution and addressing your case inbound and triage challenges. Our experts help you with:

Solution design activities including business/functional requirement analysis, solution strategy, solution design

System integration services using accelerators to deliver implementation, validation,  upgrade, project management and end user training

Data migrations and Systems migration

Fully managed regulatory compliant cloud hosting

Build adapters as per your custom source data systems for both upstream and downstream (such as safety and product complaint) systemsService desk and application support

Design and development of custom reports

All our early phase clinic automation service utilize our Optimized Global Service Delivery Model designed to make you fully compliant with regulatory requirements and industry standards.