Our dedicated teams in Marketing and Regulatory affairs departments undertake:
- Direct selling to the user of Bulk-Drugs, intermediates.
- Procuring orders from industry as Indenting Agents for overseas manufacturers of registered / un-registered Bulk-drugs and intermediates.
- Registration for imports into India of API / Finished Formulations / Cosmetics with Drug Controller General of India, Ministry of Health.
- Permission to manufacture new drugs for Marketing / Sales from FDA/DCGI.
- License for import of Drug for testing purpose.
- Registration Certificate for Medical Devices and Import Licenses thereof.
- ACTD/CTD Dossier, Process Validation & Analytical Method Validation.
- Clinical Trial.
C-8, Hari Nagar, New Delhi - 110 064 India
Fax: 91-11-45082611, Email- firstname.lastname@example.org
F-123, 3rd Floor, Anna Nagar East, Chennai - 600 102 India Mob- 91-9962076000
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