#IRT systems for clinical trails

[ddiclinical]

IRT has created its footprint in the field of clinical research and has evolved drastically in such a way that it has bought a major difference in perspective of clinical trials over the decades. It faceted itself into the streams from only randomizing the subject and assigning them to a treatment group to managing the overall supplies required throughout the study through supply management.

[vistaarai2020]

IRT has created its footprint in the field of clinical research and has evolved drastically in such a way that it has bought a major difference in perspective of clinical trials over the decades. It faceted itself into the streams from only randomizing the subject and assigning them to a treatment group to managing the overall supplies required throughout the study through supply management.

[pharmaphorumuk]

IRT Europe Summit

New clinical trial regulations are requiring sponsors to keep tighter oversight than ever before – from audit trails to tracking system changes – resulting in high costs and trial delays. IRT Europe explores implementation best practices and how interactive response technologies can be utilised to improve supply chain planning and optimise clinical trials. Take this opportunity to share and discuss current industry needs, the latest tools and solutions for forecasting and the various regulatory requirements for IRT, among many other critical topics. Register at www.cbinet.com/IRTEU.

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from Pharmaphorum https://pharmaphorum.com/events/irt-europe-summit/

[techsolcorpmarketing-blog]

Case IRT – Intake, Receipt and Triage

Techsol CaseIRT is an advanced solution for intake, Receipt and Triaging of AEs (Adverse Events) and PCs (Product Complaints). CaseIRT enables companies to harmonize their data receipt, assessment and tracking globally using one platform, leading to improved regulatory compliance and overall process efficiency. CaseIRT enables: Inbound and Receipt from affiliates, partners, medical information contact centers, suppliers and various other intake systems and third party systemsCase Triage and transmission of AEs in to safety database such as Argus Safety, ArisG via E2B/HL7 compliant adapter and PCs in to Product complaint database system such as Trackwise.In-built validation rules and duplicate searchQuality control gates at various work flow stages. Integrated rule based Retrospective Quality Assurance processGlobal and local Inbox to manage all the incoming data via various channelsIntegrated reporting and Business Intelligence capabilities. Ready to use various project management and data listings reportsFully compliant with FDA 21 CFR Part 11 regulations and provides comprehensive audit trail capabilities for all the changesHighly configurable and zero footprint web based platformAvailable 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 Techsol Services:

Our CaseIRT 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 designSystem integration services using accelerators to deliver implementation, validation, upgrade, project management, data/systems migration, end user trainingFully managed regulatory compliant cloud hostingBuild adapters as per your custom source data systems for both upstream and downstream (such as safety and product complaint) systemsService desk and application supportDesign and development of custom reportsAll our early phase clinic automation services utilize our Optimized Global Service Delivery Model designed to make you fully compliant with regulatory requirements and industry standards.