Prove legal domestic marketing status and facility regulatory compliance for medical devices, pharmaceuticals, and health exports worldwide.
A Certificate to a Foreign Government (CFG) is an official regulatory document issued by national health authorities (such as the U.S. FDA) certifying that specific medical products, drugs, or biologics are legally marketed in the originating country and that manufacturing facilities meet applicable compliance standards.
Required by overseas ministries of health before granting market authorization and import licenses for healthcare products.
Confirms that products comply with domestic safety regulations and that manufacturing facilities maintain proper establishment registration.
Streamlines customs clearance and eliminates administrative bottlenecks for critical medical and pharmaceutical exports.
CFGs are primarily issued for highly regulated sectors requiring direct government attestation.
Class I, II, and III medical equipment requiring device listing and establishment verification.
Finished drug products, active pharmaceutical ingredients, and therapeutic treatments.
Human cells, tissues, and cellular-based health products bound for global clinical or retail markets.
Regulated cosmetics, food additives, and specialized diagnostic testing kits.
A structured three-step workflow to verify establishment registration and secure your CFG.
Confirm active facility registration, product listing numbers, and adherence to current good manufacturing practices (cGMP).
Submit application paperwork detailing the exact product specifications and destination country to the regulatory authority.
Receive your official Certificate to a Foreign Government ready for submission to foreign health ministries and customs.
Need assistance with acquiring a Certificate to a Foreign Government for your medical or pharmaceutical exports? Connect with our regulatory team.