May 2018 GUDID Release - 3 Necessary and Immediate Action Steps

by Stefanie Wichansky on Apr 25, 2018 12:30:00 PM

Major Regulatory Changes for Own-Brand Label (OBL) Manufacturers 

by Stefanie Wichansky on Apr 5, 2018 1:00:00 PM

Is your Company Ready for GDPR?

by Stefanie Wichansky on Apr 3, 2018 12:16:00 PM

EU MDR - 6 Significant Impacts on Clinical Evidence

by Stefanie Wichansky on Mar 27, 2018 1:02:00 PM

EU MDR - Significant Impacts on Post-Market Surveillance

by Stefanie Wichansky on Mar 21, 2018 10:06:00 AM

The New EU MDR – A Call to Action for Manufacturers

by Mark Neal on Feb 16, 2018 11:00:00 AM

At PRP,  we believe that staying connected to Pharmaceutical and Medical Device experts is paramount to gathering the key information necessary to...

MDSAP Is Here, What Medical Device Manufacturers Need to Know

by Stefanie Wichansky on Feb 16, 2018 10:30:00 AM

The Medical Device Single Audit Program (MDSAP) allows for medical device manufacturers to undergo a single regulatory audit that covers the...