PDS is a leading global provider of software and solutions dedicated to preclinical research and development. Our intuitive products and outsourced services accelerate the development and regulatory submission of pharmaceutical and biotechnology products.
Regulatory Submission and Management
TranSEND™ is your complete submission solution to get your preclinical data ready for the FDA’s Standard for Exchange of Nonclinical Data (SEND) requirements. From assessment, to implementation, to comprehensive submission guidance, PDS is your all-in-one partner for SEND, even when dealing with legacy data or output from other information systems.
The Turnkey Service for FDA SEND-compliant Submissions
SEND Express™ is your one-stop shop for outsourced Standard for Exchange of Nonclinical Data (SEND) dataset generation and has been used successfully for dozens of trial and registration FDA SEND submissions.