Partnering Solutions
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A Definitive Guide To The Site Enablement Maturity Assessment
11/14/2023
Clinical research sites play a crucial role in data collection, patient interactions, and protocol procedures. Utilize this methodology for uncovering site enablement capability maturity.
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Virtual Investigator Meetings By Advarra
6/10/2021
Advarra’s unmatched, comprehensive suite of training services helps sponsors and CROs ensure efficient and compliant training at their sites. Powered by Longboat, Advarra can create custom protocol training and deliver training to site staff via a sleek, intuitive 21 CFR Part 11 compliant platform.
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APAC Biopharma: Bridge The Gap To The US FDA
2/8/2024
Uncover how these regulatory and partner/outsource services are invaluable for biopharma innovators in navigating the U.S. FDA regulatory process.
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Manage Contracts And Legal Documents With Ease
7/6/2022
Handle all aspects of contract and template development, from alternative language and budget parameter development to patient reimbursement with ease.
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Advancing Development And Approval Of Rare/Ultra-Rare Disease Therapies
5/8/2024
VeriStat empowers rare disease therapy with science-driven strategies and trusted expertise, supporting over 350 rare disease projects and preparing 40+ marketing applications in the past 5 years.
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Running Successful Clinical Programs Using A FSP Model
3/27/2023
Specialized, demand-driven resourcing from Veristat ensures a clinical team’s focus remains where it should be: meeting study milestones and accelerating time to market.
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Improve eCOA Data Collection And Clinical Trial Efficiency
4/18/2023
Ameliorate your eCOA data collection and clinical trial efficiency with Kayentis and ClinOne's combined solution, covering eCOA, virtual visits, consent management, patient engagement, and more.
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Site Contracts & Payments
3/20/2023
Discover how ThoughtSphere’s SPACE solution can cultivate these important partnerships by accelerating payment cycles, reducing financial errors, and enhancing relationships through collaboration, transparency, and more.
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An Introductory Guide To Clinical EU Qualified Person (QP) Services
10/3/2022
PCI's team of qualified persons assume responsibility for all stages of the process, safeguarding patients including the audit of the supply chain for GMP compliance in addition to certification of products for use in clinical trials.
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Advarra Regulatory Consulting
6/10/2021
Our regulatory consultants take action and move your research forward. If you’re looking for help in the development of innovative life science and digital health products, then Advarra® is the answer.