As a Premiere Services Partner, USDM has been helping Veeva customers reduce their implementation and validation time since 2015, with over 200 Veeva projects successfully completed. Visit our booth at Veeva’s R&D and Quality Summit in Boston.
UPCOMING WEBINAR: Please join our panel of experts, including Francisco Vicenty, Program Manager, Case for Quality, FDA, to discuss any changes and implications impacting medical devices, pharma, and biotech organizations.
Our Emerging Leadership Team will be attending #BIO2022 and we invite you to meet with them to discuss how we help startups establish their overall IT strategy and rapidly execute a compliant IT framework.
ON-DEMAND WEBINAR: Learn how USDM customized various workflows, demonstrated a framework for continuous compliance, and responded to detailed questions about regulatory requirements for each of the featured customers.