Navigate global pharmaceutical trade with confidence. Source APIs, generics, and medical devices from certified manufacturers — with full regulatory compliance guidance for every destination market.
8
Products covered
7+
Sourcing countries
8
Certifications
4
Destination markets
$1.4T+ annual trade
Annual trade volume
WHO Good Manufacturing Practice
Baseline international GMP standard; mandatory for WHO prequalification and many national authorities.
VerifyEU Good Manufacturing Practice (EMA)
Required for pharmaceutical products marketed in the European Union. EMA oversight.
VerifyUS FDA 21 CFR cGMP Approval
FDA site inspection and registration for US market pharmaceutical manufacturing.
VerifyISO 13485 Medical Device QMS
Quality management system standard specific to medical device manufacturing.
VerifyPharmaceutical Inspection Co-operation Scheme
International GMP harmonization; PIC/S member country GMP certificates widely recognized.
VerifyHalal Pharmaceutical Certification
Required for pharmaceutical and supplement exports to Gulf and Muslim-majority markets.
VerifyCE Marking for In Vitro Diagnostics
EU conformity marking for in vitro diagnostic medical devices under IVDR 2017/746.
VerifyICH Q7 Good Manufacturing Practice for APIs
International standard for active pharmaceutical ingredient manufacturing.
Verify