European Medical Device Regulation

Never miss these while writing the “Common Technical Document (CTD) for Pharmaceutical”

Never miss these while writing the “Common Technical Document (CTD) for Pharmaceutical”

Scientific Regulatory writing is a complex process due to its dossier size, data complexity, and submission deadlines and it requires...

Challenges in the CRO Industry: Selecting a CRO for your Research Trials

Challenges in the CRO Industry: Selecting a CRO for your Research Trials

Clinical Research Organization for Healthcare provides clinical-study and clinical-trial support for drugs and medical devices, wherein many pharmaceuticals, biotechnology, and...

New MEDICAL DEVICE REGULATION(MDR): Top 5 Challenges

New MEDICAL DEVICE REGULATION(MDR): Top 5 Challenges

Within the medical devices industry, professionals have long been exercising acquiescence with regards to the new European Medical Device Regulation...