PDS – Committed to Compliance
PDS was founded in 2005, initially providing Patient Information services. Over the course of the following decade we have grown steadily, whilst expanding our portfolio. Today we offer our clients a complementary range of professional pharmacovigilance and regulatory services. We are a forward thinking company and a significant step in our development came in 2012, when we introduced xEVMPD services to our portfolio. Following thousands of successful submissions for our clients, we are now recognised as a leader in this field as we move into the era of IDMP.
As a partner of choice for numerous high profile life-sciences companies, (including some of the world’s Top 5 pharma), we continue to build on our reputation for being a trusted outsource partner, committed to delivering detailed responsive solutions through strategic thinking, depth of professional ability and a commitment to the highest quality standards.
We are highly TEAM driven and focused on adding value to our clients business, meaning we aim to be much more than just another service provider who reacts; instead we proactively support our clients with sound professional advice and through highlighting potential roadblocks before they arrive, to help ensure they remain compliant at all times.
Clinical trial design, management & consulting, Medical writing