We provide complete regulatory services for medical device importers, manufacturers, and suppliers. Our team is experienced in handling quick regulatory submissions and approvals.

New Drug Approval Manufacturing Licence (Form 25/28) Import & Registration Certificate Product Permission Stability & Technical Documentation Support

Blood Centre Establishment Licence Blood Storage Centre Approval Renewal & Compliance Documentation NABH / Regulatory Support

MD-5 – Manufacturing Licence MD-14 – Import Licence MD-9 – Wholesale Licence MD-26 – Loan Licence Device Registration & Regulatory Submissions

r-DNA Products Approval Vaccine Approval Process CDSCO Biologicals Division Submissions Import & Testing NOC Post-Approval Changes

Import Registration Certificate (IRC) Manufacturing Licence (Form 32/33) Label Review & Compliance New Cosmetic Product Registration

Import Licence (Drugs & Devices) Export NOC / CoPP Assistance Registration of Foreign Manufacturers Clearance Support & Documentation

Clinical Trial NOC (Phase I–IV) Ethics Committee Registration Protocol Review & Submission SAE Reporting & Regulatory Compliance

BA/BE Centre Approval CDSCO Permission for Studies Protocol Review & Submission Study Report Regulatory Filing
Together we can help you achieve your goals. Consult
with our corporate business consultants to get the right
solutions for your business. Get help with your funding
and investments, find the right strategies for your growth plan and watch your business expand.