CDSCO Consultant
The Central Drugs Standards Control Organisation, in short CDSCO, is a regulatory body that issues certificates for medical device import and manufacturing, cosmetics import and manufacturing, medicine import and manufacturing, ADC NOC, dual-use NOC, blood bank registration, ethics committee registration, BA/BE, etc. Connect with India most reputed advisor and consultant, Agile Regulatory, to know…
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CDSCO Registration
The registration provided by the Central Drugs Standard Control Organisation for manufacturing, import, distribution and sale of drugs, cosm…
View detailsCDSCO Import License
The process of importing a medical device, drug or cosmetic product in India is not only a customs clearance process but also a regulatory p…
View detailsCosmetics Import License
If you are planning to import cosmetic products into India, it is mandatory to obtain Cosmetics Import Registration. Agile Regulatory provid…
View detailsMedical Device Import License
Medical Device Import Registration (FORM MD-14, FOR MD-15) has been issued by the Central Drugs Standard Control Organization (CDSCO) to an…
View detailsMedical Devices Registration in India
CDSCO Medical Device Registration has been required for Manufacturers, importers, wholesalers, and distributors of Medical Devices and diagn…
View detailsMedical Device Manufacturing License
A Medical Device Manufacturer Registration Certificate has been issued by CDSCO (Central Drugs Standard Control Organization) to domestic ma…
View detailsDrug Manufacturing License Registration
It is mandatory to obtain a drug manufacturing license for companies planning to manufacture drug products in India. The process involves su…
View detailsCDSCO Certification in India for Medical Device, Drugs, and Cosmetics (2026 Update)
If you’re planning to sell medical devices, drugs, or cosmetics in India, you’ll need CDSCO certification. It’s the govern…
View detailsThe Filing Process
The same four stages, every certificate
- 01
Free Consultation
We map your product or business against the regulators that apply to it, and flag what's realistic before any paperwork begins.
- 02
Documentation
Our advisors prepare and cross-check every form, test report and certificate the filing requires.
- 03
Application Filing
We submit through the correct portal or authority, and track the file until the regulator responds.
- 04
Certificate Granted
You receive the certificate or license, plus a renewal timeline so it never lapses unnoticed.