SSCP for Devices: Challenges and Approach
As per EU MDR, for class III and implantable devices (other than ...
6 Best Practices to Navigate and Sustain Regulatory Labeling Compliance
It has always been a difficult task to be compliant with the chan...
RAPS – 2019 Regulatory Convergence Round-up by MakroCare
Recently concluded RAPS- 2019 regulatory convergence at Philadelp...
Deadline Extended for DMF Type III eCTD Submissions by FDA
This being the third time in a row, the United States Food and Dr...
Regulatory CMC Changes for Pharmaceutical Products
All the biopharmaceutical companies must follow respective nation...
Post-Market Surveillance Planning and Challenges under EU MDR
PMS is a collection of processes and activities used to monitor t...
