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DGFT_Compliance_services_in_India_-_Corpseed.webp
DGFT Compliance services in India
by Parul Bohral on 2025-05-06

The Directorate General of Foreign Trade (DGFT) is an agency working under the Ministry of Commerce and Industry, Government of India. It is the chief authority responsible for implementing the country's foreign trade policy.

Drug_and_Cosmetic_Rules_Corpseed.webp
Drugs and Cosmetics (Compounding of Offences) Rules, 2025: Bridging Regulation and Business Continuity
by Mahek Sancheti on 2025-04-28

The Drugs and Cosmetics (Combination of Offences) Rules, 2025, the accused can apply to the Compounding Authority, offering a monetary penalty to resolve the issue. The authority reviews the case, consults with relevant bodies and may grant exemption from prosecution if conditions are met.

FSSAI_Registration_for_Swiggy_Corpseed.webp
FSSAI Registration for Swiggy: A Complete Guide for Food Business Operators
by Parul Bohral on 2025-04-17

The Food Safety and Standards Authority of India (FSSAI) is a government body established under the Food Safety and Standards Act, 2006.

CDSCO_MD16_Form_Corpseed.webp
The Impact of CDSCO MD-16 Form on India's Medical Device Industry
by Mahek Sancheti on 2025-04-10

The CDSCO MD 16 form is an application used to seek a license for the import of medical devices into India for purposes such as clinical  trials, product testing, demonstration, or training.

Everything_You_Need_to_Know_About_CDSCO_COS-1_and_COS-2_Corpseed.webp
Everything You Need to Know About CDSCO COS-1 and COS-2: The Essential Guide for Importers & Manufacturers in India
by Parul Bohral on 2025-04-09

In India, the directive of cosmetic products is supervised by the Central Drug Standard Control Organization (CDSCO), which ensures that all cosmetics fulfill the required safety, quality, and efficiency principles before they reach the market.

CDSCO_MD7_Corpseed.webp
The Role of CDSCO MD7 in Ensuring the Safety and Quality of Medical Devices in India
by Mahek Sancheti on 2025-04-09

The CDSCO MD7 is a specific form designed to apply for manufacturing licenses for medical devices classified under Class C and Class D for retail or wholesale distribution.