The clinical trial industry is highly regulated with a complex landscape. Contract Research Organizations (CROs) are a big part of any strategic product development life cycle. Sponsoring companies of new drugs, devices or biologics may outsource all or part of their clinical research. These service providers or vendors range from niche to full service capabilities, which a sponsor of a clinical trial(s) would need to define and assess. Procurement of the best fit CRO involves a variety of processes and people.
This webinar evaluated the following:
- Determining internal champions/selection committees
- Strategic Sourcing/Procurement workflow/checklist
- Documentation and Regulations
- Challenges of CRO Outsourcing
- Best Practices to get best value
If you'd like to watch a recording of the webinar, complete the form to get started today.
To download the CRO Selection (RFP) Checklist mentioned in the webinar, click here.
ShareVault’s secure document sharing solution gives medical device, diagnostics, biopharma and many organizations the confidence to simply and securely share sensitive documents with third parties during due diligence, product development, collaborative research and other confidential file sharing activities.
Compared to consumer-grade solutions, ShareVault virtual data rooms offer many features that give you control and document intelligence with the highest level of document-protection and monitoring available. Learn more.