Validant is proud to sponsor the MedTech Summit on EU MDR & IVDR this June 17 – 21 in Brussels. Topics include regulatory and clinical strategies, PMS & vigilance, legal, combination products, sterilisation and emerging market requirements. Join Validant EU Regulatory Consultant, Ginger Swassing, as she presents on EU MDR and IVDR frequently asked questions related to Quality Systems and Technical Documentation. Use our exclusive discount VIP code CQ7132VLD for 25% off your ticket.
With Validant, I have the opportunity to work with pharmaceutical companies worldwide that are working to positively impact patient health. My skills from 37 years in industry in Quality System Implementation and Quality Remediation are directly applicable to help our clients.
John M. | Validant Managing Partner since 2016
Validant offers win-win solutions for clients and consultants, continually building and maintaining lasting relationships. Their experts in business development and recruiting ensure that subject matter expertise and skill set is matched for the client and the best consultants are placed on the project.
Janet W. | Validant Consultant since 2013
In the spring of 2015, my firm had a significant FDA audit with serious findings concerning sterility assurance and data integrity. We had utilized Validant for a previous engagement successfully. Before the audit concluded, I was already in contact with the Validant team for assistance. I was very impressed by how quickly they orchestrated data integrity audits at all of our 20+ other sites. We then turned to them for assistance with our third-party oversight of our manufacturing operation and quality control laboratories.