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Country of origin : India

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urofollitropin

Injection 75 IU, 150 IU, 300 IU, 900 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #23023

Established in 2008, the manufacturer excels as a CTD dossier owner and manufacturer, distributing its pharmaceutical products across multiple countries. Renowned as a GMP manufacturer, it employs state-of-the-art production lines specifically designed to meet stringent quality standards, essential for a CTD dossier owner and manufacturer. This underscores their commitment to excellence and safety in drug manufacturing, ensuring they maintain their status as a leading CTD dossier owner and manufacturer.

 

 

 

 

Manufacturer usually replies in 3 days

urofollitropin

Vials, lyophilized 300 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #10170
A pharmaceutical manufacturer providing export-oriented development and commercial supply of pharmaceutical products across a complete range of finished dosage forms, including tablets, capsules, softgels, injectables, ointments, dry syrups, and sachet presentations. The organisation positions itself as a licensing-and-supply partner with integrated manufacturing expertise and a growing international portfolio, and it reports holding multiple regulatory approvals from major global authorities (including MHRA, TGA, ANVISA and GCC regulators) alongside WHO-GMP compliance for its manufacturing operations, supporting consistent quality and reliability of pharmaceutical products for overseas partners.

Manufacturer usually replies in 29 days

urofollitropin

Vials, lyophilized 75 IU, 150 IU

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #10170
A pharmaceutical manufacturer providing export-oriented development and commercial supply of pharmaceutical products across a complete range of finished dosage forms, including tablets, capsules, softgels, injectables, ointments, dry syrups, and sachet presentations. The organisation positions itself as a licensing-and-supply partner with integrated manufacturing expertise and a growing international portfolio, and it reports holding multiple regulatory approvals from major global authorities (including MHRA, TGA, ANVISA and GCC regulators) alongside WHO-GMP compliance for its manufacturing operations, supporting consistent quality and reliability of pharmaceutical products for overseas partners.

Manufacturer usually replies in 29 days

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