Our full-service regulatory affairs team specializes in providing services and support to meet the regulatory needs of small to mid-sized pharmaceutical, biotechnology, and device companies. Our flexible sourcing model augments existing skill sets for today’s smaller life science companies, ensuring regulatory compliance.Do you have a regulatory question or
You will be contacted
within 48 hours
Built entirely in the cloud, rsDM is a SaaS-based solution with no installation or download required. Fully 21 CFR Part 11 compliant, rsDM's cloud-based model changes the way our industry handles document management. It's easy and requires no IT support - perfect for today's smaller, more virtual life sciences companies.Discover cloud based document management today.
VRS offers focused Regulatory strategy, services and technologies specifically designed to meet the needs of growing biopharma companies in developing and registering new therapies in major markets.
VRS provides an industry leading, comprehensive solution, combining top tier Regulatory strategy experts with simple, cloud-based document management technology that supports collaborative authoring, review and approval processes. With practical experience combined with regulatory processes and accountability for results, we are focused on getting clients “across the finish line.”