Medical Devices – USA/Europe Regulatory Updates Roundup, Mar 2022
EUROPE (EU), USA (FDA)
EUROPE (EU) SIQ Ljubljana became a notified...
Medical Devices – Asia Regulatory Updates Roundup, Mar 2022
INDIA (CDSCO)| PAKISTAN (DRAP) | PHILIPPINES (FDA) | CHINA (NMPA) ...
A Guide for Medical Device Organizations in Clinical Evaluation Report (CER) Submission
Launching a new medical device in the market always need a Clinica...
8 key Questions & Responses on Clinical Investigation under EU MDR
1: Difference between the performance, clinical performance and cl...
Medical Devices – USA/Europe Regulatory Updates round up Dec-2021
EUROPE| US FDA | United Kingdom | CANADA (HC) |ARGENTINA
EUROPE Co...
Medical Devices – Asia Regulatory Updates Roundup Dec 2021
India (CDSCO) | Vietnam (MOH)| SINGAPORE (HSA, SINGCERT) | Austral...
