Tag: ROW Regulatory News

Pharma/Biotech – Asia, ROW Regulatory News, July 2023 Vol. 2

July 26, 2023
Biopharma

ASIA Singapore Guidance on therapeutic product registration in Singapore This guidance document describes the procedures and requirements for submitting an application to register a therapeutic...

Asia Regulatory News, BioTech, New Molecular Entities, Pharma, Regulatory Updates, ROW Regulatory News, Swissmedic, Therapautic Product

Medical Devices-Asia and ROW Regulatory News-July 2023

July 25, 2023
Medical Device

ASIA SINGAPORE (HSA) HSA’s SRA status for In-vitro Diagnostic Medical Devices (IVD) An SRA is a national health products regulatory authority considered by the WHO to apply stringent...

Asia Regulatory News, IVD, Medical Devices, Regulatory News, ROW Regulatory News

Pharma/Biotech – Asia, ROW Regulatory News, June 2023 Vol. 2

June 21, 2023
Biopharma

ASIA India India starts mandatory tests of exported cough syrups after child deaths India will require manufacturers of cough syrups to acquire a Certificate of Analysis (CoA) from a designated...

Asia Regulatory News, BioTech, Pharma, Regulatory Updates, ROW Regulatory News

Medical Devices-Asia and ROW Regulatory News-June 2023

June 20, 2023
Medical Device

ASIA INDIA (CDSCO) 2023.06.02_MDR_Final G.S.R. 409(E)_Amendment in Rule 18 and 19 for notifying State MDTL The State Government may, by notification, establish State Medical Devices Testing...

Asia Regulatory News, Implantable Medical Devices, In-vitro Diagnostic, IVD, Medical Devices, Regulatory News, ROW Regulatory News

Pharma/Biotech – Asia, ROW Regulatory News, April 2023 Vol. 2

April 20, 2023
Biopharma

ASIA Malaysia Declaration of Worldwide Registration Status for Generic Medicines in QUEST System All new applications for Generic Medicines (Prescription-Full) shall declare...

ANVISA, Asia Regulatory News, BioTech, Chemistry, eCTD, Manufacturing and Control (CMC), Pharma, Regulatory Updates, ROW Regulatory News

Medical Devices-Asia and ROW Regulatory News – April 2023

April 18, 2023
Medical Device

ASIA INDIA (CDSCO) Circular for Licensing of Class C & D medical devices According to the Circular It is pertinent to mention that as per Medical Devices rules (MDR) 2017 manufacturing...

Asia Regulatory News, Medical Devices, Regulatory News, ROW Regulatory News, SaMD, Software as a Medical Device