Скачать или смотреть SUGAM Portal Step-by-Step | 15 Essential FAQs for Pharmaceutical Import & Registration

Thinking about importing or registering pharmaceutical products in India? In this video, CliniExperts takes you through 15 must-know FAQs about the SUGAM Portal, the official CDSCO e-governance platform for drug import and registration.
Regulatory Expert at CliniExperts, shares insights from over 15 years of experience helping Indian importers and global manufacturers secure faster, smoother, and fully compliant approvals.
What you’ll learn in this video:

✅ How the SUGAM Portal works for pharmaceutical registration and import licensing

Expert answers to the 15 most common CDSCO FAQs - including Forms 41, 10, 10A, fees, timelines, and common mistakes to avoid
How CliniExperts can reduce your approval timeline by up to 30%

Video includes:
FAQ 1: Drug import regulations in India
FAQ 2: What is the SUGAM Portal?
FAQ 3: Who can apply for a Registration Certificate or Import Licence?
FAQ 4: Understanding Form 41
FAQ 5: Difference between Form 10 and Form 10A
FAQ 6: Documents required for Form 41
FAQ 7: Registration & import fees
FAQ 8: Multiple drugs on one certificate
FAQ 9: Is pre-inspection mandatory?
FAQ 10: Approval timelines
FAQ 11: Common SUGAM mistakes
FAQ 12: Tracking your application
FAQ 13: Re-registration process
FAQ 14: Responding to CDSCO queries
FAQ 15: Why choose CliniExperts?
Why watch?

Whether you’re an Indian importer or a foreign manufacturer entering the Indian market, this video gives you a step-by-step understanding of the SUGAM Portal process, backed by real regulatory expertise.
Need expert help?

Visit: https://cliniexperts.com to book a consultation and get your CDSCO submissions right the first time.
CliniExperts -A pharma regulatory consultants. Regulatory support services for Medical Device/IVD, FSSAI, Drugs, Biologicals.
Call +91 7672005050