Webinar: Understanding EU MDR Post-Market Surveillance Challenges and Requirements

Regulatory Compliance Associates and AMPLEXOR Life Sciences have joined forces to bring you this webinar about Understanding EU MDR‘s Post-Market Surveillance Challenges hosted by our own Stephen Coulter. The main focus of the webinar is to cover the best practices relating to implementing a compliant EU MDR PMS platform. We will have 2 sessions on February 27th, one at 5:00 am MST and one at 11:00 am MST. To register Online Follow the link below.

I'm Interested in Learning More About RCA

News

Regulatory Pathways for Medical Device and Pharmaceutical Filings and cGMP Compliance Considerations...
Read More

News

Regulatory Pathways for Medical Device and Pharmaceutical Filings and cGMP Compliance Considerations...
Read More

News

Regulatory Pathways for Medical Device and Pharmaceutical Filings and cGMP Compliance Considerations...
Read More
PharmTech PDA Podcast – 2019 PDA Quality Week...
Read More
Calling All Active PDA Members – Vote Now in PDA’s 2020 Officers and Board of...
Read More