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I will assist you with cdsco approvals
Devansh K
About this gig
Getting CDSCO approval isn't complicated if you know what you're doing. Most delays come from wrong classification, incomplete documentation, or poorly handled queries not from the regulation itself.
I assist importers and manufacturers with CDSCO approvals across three product categories:
Drugs and pharmaceuticals
Import license applications for new drugs and formulations, manufacturing license support, and documentation for products requiring CDSCO clearance before entering the Indian market.
Cosmetics
COS-1 import registration under the Cosmetics Rules 2020, including formulation and ingredient compliance review, manufacturer authorization, Power of Attorney drafting, and query response until registration is granted.
Medical devices
MD-14/MD-15 import license applications for Class A, B, C, and D devices including SAMD and SiMD. Covers device classification, technical dossier review, authorized agent setup, and end-to-end query management.
For every project I review the product and documentation before filing so the application goes in complete, not corrected after the first rejection.
Message me with your product details before ordering so I can confirm the exact requirements f
Get to know Devansh K
Devansh K
Regulatory Affairs Consultant, CDSCO, FSSAI ,Medical Device Licensing Expert
- FromIndia
- Member sinceJun 2026
- Avg. response time3 hours
Languages
Hindi, English
Regulatory affairs consultant in India, specializing in CDSCO drug, cosmetic & medical device approvals, FSSAI registration, State FDA licensing, sanitary import permits, and SAMD/SiMD device registrations. 25+ clients served across food, pharma, and device sectors. I handle every project personally, helping you avoid wrong category selection, weak documentation, and stuck regulatory queries.
My Portfolio
Other Regulatory Compliance Consulting Services I Offer
FAQ
Do you guarantee approval?
No consultant can guarantee a regulatory approval — anyone who says otherwise is being dishonest. What I guarantee is a clean, complete, well-documented application that gives you the best shot at approval without avoidable delays.
Which states and device classes do you cover?
CDSCO approvals are central — they apply pan India. I cover all medical device classes A through D including SAMD and SiMD, and all drug and cosmetic categories under CDSCO's purview.
My application is already stuck in queries. Can you help?
Yes. Share the query details and existing documentation and I'll review it and advise on next steps. Message me first to discuss.
Do I need to share confidential formulation data?
Only what is required for the actual application. Everything shared is treated as confidential.
