rDNA

Post Approval changes for clinical trials (Form CT-06) for CGTP through SUGAM Online Portal

Posted by: Prabhas Chakraborty November 7, 2025

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7th November, 2025

2025.10.16_ G.S.R. 758(E)_ Inclusion of additional items under CLAA in Drugs Rules 1945

Posted by: Hitesh Gupta November 3, 2025

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3rd November, 2025

Circular to all State/UT Licensing Authorities regarding recent revised GST rate Structure

Posted by: Prabhas Chakraborty October 16, 2025

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16th October, 2025

Processing of Grant of WHO GMP COPP applications in respect of products under consideration for license approval through ONDLS Portal

Posted by: Prabhas Chakraborty October 9, 2025

Acceptance of the IBSC approval for seeking permission to manufacture test items for examination, test and analysis through form CT-10 as per the recommendation of the 314th RCGM meeting, dated 09.07.2025

Posted by: Hitesh Gupta September 11, 2025

What's New 2?

Regulation/Guidelines

Documents Required for Cosmetic Import License in India (Checklist 2026)

The Central Drugs Standard Control Organization (CDSCO) is responsible for issuing Cosmetic Import licenses in India. Importers must apply through the SUGAM portal using Form COS-1 for fresh products. After...

13th April, 2026

Regulation/Guidelines

Regulatory Due Diligence for Medical Devices in India: What Manufacturers Must Know Before Market Entry

Regulatory Due Diligence for Medical Devices in India is essential for manufacturers planning to enter the country’s rapidly growing healthcare market. Proper regulatory assessment ensures compliance with CDSCO guidelines, licensing...

31st March, 2026

Regulation/Guidelines

How to Apply for BIS Certification in India: Process, Documents & Timeline

Businesses planning to apply BIS certification India must understand the regulatory framework governed by the Bureau of Indian Standards. The BIS certification process ensures product quality, safety, and compliance with...

23rd March, 2026

Regulation/Guidelines

Regulatory Pathway for Biologicals in India: Approval Process & Key Requirements

The Regulatory Pathway for Biologicals in India is governed by strict guidelines to ensure the safety, efficacy, and quality of biological products. Manufacturers must follow regulatory frameworks established by CDSCO...

23rd March, 2026

rDNA

rDNA

Post Approval changes for clinical trials (Form CT-06) for CGTP through SUGAM Online Portal

2025.10.16_ G.S.R. 758(E)_ Inclusion of additional items under CLAA in Drugs Rules 1945

Circular to all State/UT Licensing Authorities regarding recent revised GST rate Structure

Processing of Grant of WHO GMP COPP applications in respect of products under consideration for license approval through ONDLS Portal

Acceptance of the IBSC approval for seeking permission to manufacture test items for examination, test and analysis through form CT-10 as per the recommendation of the 314th RCGM meeting, dated 09.07.2025

For Importers To India

Drug

Biologicals

Food Supplements

Medical Device

IVD

Food

Cosmetic

Other

For Manufacturer in India

Drug

Biologicals

Food Supplements

Food

Medical Device

IVD

Cosmetic

Other