Blogs
Medical Devices-USA/Europe Regulatory…
USA (FDA)
Peripheral Percutaneous Transluminal Angioplasty (PTA) and Specialty Catheters – Premark…
Regulatory Reporting Software –…
The pharmaceutical manufacturing industry has been rapidly evolving. The manufacturers of d…
Pharma/Biotech – Asia, ROW Regu…
ASIA
Malaysia
Declaration of Worldwide Registration Status for Generic Medicines in QUEST Syste…
Medical Devices-Asia and ROW Regulato…
ASIA
INDIA (CDSCO)
Circular for Licensing of Class C & D medical devices
According to th…
MDR Regulations – Impact on Med…
The EU Medical Device Regulation (MDR) has been in effect since May 26, 2021 and has had a …
Pharma/Biotech – USA, Europe Re…
USA
FDA Issues Guidance on ISO Data Standards for Medicinal Products
As part of its efforts to …
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