The design and develop-ment of sample manage-ment solutions compliant with PDMA regulations is, to say the very least, a complex undertaking and not one that all software companies find easy to get their arms around. 

With 25 years experience in document and information management, plus a deep involvement with PDMA regulations and regulators from the start, DRS has the credentials to assist life sciences companies with every or any phase of the samples management process.

Through our PDMA OneSource suite of products and solutions, clients have access to all options: production services, information capture, custom software, data storage, as well as full integration into back-end systems.

Our modular approach to software offerings allows

us to find the right mix of
products and services to fit any corporate budget and business need. 

The process is simple -- existing business logic is evaluated, a plan of action is developed, and recommendations for improvement based on our experience in regulated industries, information processes and reporting are presented. 

In addition, our ClientsFirst approach includes presenting the proper tools and services to manage a validated and fully compliant operation which will stand up to the Federal PDMA standards.  

Fully Validated software solutions through our PDMA OneSource suite of products

Modular approach to implementing each component

SaaS models utilized when preparing the business case

PDMA compliant systems and services to complete the offering on site or off site