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...