Form I

Retention of Loan Manufacturing License for Class A and B Medical Devices in India – MD 4 & MD 6

Posted by: Neha Gupta June 14, 2023

Retention of Manufacturing License for Class C and D Medical Devices in India – MD 7 & MD 9

Posted by: Jitendar Chauhan June 14, 2023

BIS certification for domestic manufacturer in India – Form V

Posted by: Jitendar Chauhan May 15, 2023

7
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15th May, 2023

BIS CRS for Foreign manufacturer for electronic and IT Products in India – Grant letter & Form I

Posted by: Jitendar Chauhan May 10, 2023

BIS certification for foreign manufacturer in India – Form V

Posted by: Jitendar Chauhan May 10, 2023

7
Comments Off on BIS certification for foreign manufacturer in India – Form V
10th May, 2023

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

Form I

Form I

Retention of Loan Manufacturing License for Class A and B Medical Devices in India – MD 4 & MD 6

Retention of Manufacturing License for Class C and D Medical Devices in India – MD 7 & MD 9

BIS certification for domestic manufacturer in India – Form V

BIS CRS for Foreign manufacturer for electronic and IT Products in India – Grant letter & Form I

BIS certification for foreign manufacturer in India – Form V

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