Moving to the Cloud can be an easy choice for regulated Life Science companies. USDM's Cloud VAP offers a subscription compliance model.
The USDM Life Sciences Clinical Practice is a global service provider offering strategic services and solutions for both in-house and outsourced pharmaceutical and medical device development in all phases and therapeutic areas. Our clients are offered a full menu of services and solutions to foster quality and compliant clinical trials startup, conduct, closure and submission.
Our Clinical Practice specializes in GCP Compliance and Quality Assurance, Quality Systems, Data Management, Biostatistics and Programming, Drug Safety and Pharmacovigilance, as well as Medical Writing.
We have the operational flexibility to provide development services on a stand-alone basis or as part of an integrated “full service” solution. We offer services that can be customized to each of our client’s specific needs and manage our projects in a way that guarantees a streamline, quality and timely delivery.
The USDM Life Sciences Clinical Practice has maintained, and continues to grow, alliances with key clinical system providers. We facilitate and manage projects that span the entire clinical trial lifecycle for companies of any size.
In a nutshell, the USDM Life Sciences Clinical Practice provides our clients (from start-up Biotech to large Pharma/Device) with the latest technology, processes and strategies to assist with efficiency, quality and compliance in any scenario and offers our clients a cost-effective, proactive and unified partnership in goal achievement.
You can read more about our services and solutions by visiting the links to the right. Please contact us directly if you have questions or need more information.