Pharma Ingredients & CDMO · United Arab Emirates
Importing APIs, excipients, intermediates and contract manufacture from India to the United Arab Emirates
Active pharmaceutical ingredients, excipients and pharmaceutical intermediates sold as bulk material against a specification, plus CDMO and CMO contract-manufacturing capability sold as access to a site and a process. Finished dosage forms bound for the United States are explicitly excluded: a finished drug product needs an ANDA or NDA holder of record, state-level wholesale distributor licensing and DSCSA serialization at the unit level, none of which Indiasay holds or arranges. What a buyer qualifies here is the substance and the site, not a brand.
HS classification
HS Chapter 29 (organic chemicals) for most bulk actives, intermediates and synthetic excipients; HS Chapter 28 for some inorganic actives. HS 3003/3004 (formulated, dosed medicaments) does not apply to anything in this category — see the exclusion below.
Documentation for United Arab Emirates
- MOHAP (Ministry of Health and Prevention) registration of the active/raw material for import — a separate registration track from finished-drug-product approval
- GMP certificate from the country of origin's regulator, legalised for use in the UAE
- Import permit issued per shipment against the MOHAP registration
MOHAP registers the raw material; it does not evaluate or approve whatever finished product a UAE buyer intends to make from it — that is a separate filing the buyer's own regulatory team carries.
Certifications that matter
Order volume and shipping
Courier for regulatory/development-quantity samples; air freight for early qualification lots; ocean freight (drums, fibre drums, IBC totes) for commercial-scale API and excipient volumes. CDMO/CMO capability has no shipping mode of its own — output ships under whichever mode its finished output requires.
Indiasay listings are built to be orderable from a single sample unit — MOQ and lead time are set per product, not per category, so test before committing to volume.
Listings
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Request accessPharma Ingredients & CDMO — United Arab Emirates FAQ
What HS code does APIs, excipients, intermediates and contract manufacture fall under when exporting from India?+
APIs, excipients, intermediates and contract manufacture typically falls under: HS Chapter 29 (organic chemicals) for most bulk actives, intermediates and synthetic excipients; HS Chapter 28 for some inorganic actives. HS 3003/3004 (formulated, dosed medicaments) does not apply to anything in this category — see the exclusion below..
What documentation is required to import APIs, excipients, intermediates and contract manufacture from India into the United Arab Emirates?+
Importing APIs, excipients, intermediates and contract manufacture into the United Arab Emirates requires: MOHAP (Ministry of Health and Prevention) registration of the active/raw material for import — a separate registration track from finished-drug-product approval; GMP certificate from the country of origin's regulator, legalised for use in the UAE; Import permit issued per shipment against the MOHAP registration.
What certifications matter when importing APIs, excipients, intermediates and contract manufacture from India to the United Arab Emirates?+
The certifications that matter are: MOHAP raw-material registration, Certificate of Analysis per batch, GMP certificate, country of origin.
Is APIs, excipients, intermediates and contract manufacture regulated as a food, a drug, or something else in the United Arab Emirates?+
MOHAP registers the raw material; it does not evaluate or approve whatever finished product a UAE buyer intends to make from it — that is a separate filing the buyer's own regulatory team carries.
How is APIs, excipients, intermediates and contract manufacture shipped from India?+
Courier for regulatory/development-quantity samples; air freight for early qualification lots; ocean freight (drums, fibre drums, IBC totes) for commercial-scale API and excipient volumes. CDMO/CMO capability has no shipping mode of its own — output ships under whichever mode its finished output requires.
Can I order a sample of APIs, excipients, intermediates and contract manufacture before committing to a full container?+
Indiasay listings are built to be orderable from a single sample unit or a small mixed set from USD 200, at the supplier's wholesale rate — MOQ and lead time are set per product, not per category, so a buyer can test before committing to pallet or container volume.