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protamine sulfate

Solution for injection/infusion 10 mg/ml - 5ml

Dossier type
EU CTD
Dossier status
Under development
Country of origin
European Union
GMP approvals
France
Available for
Licensing with supply, Distribution only
Manufacturer #13897
This company is a leading developer, producer, and distributor of pharmaceuticals and medical consumables, with a focus on prescription medications (Rx) for the EU market. They specialize in in-licensing and out-licensing Rx molecules, addressing market shortages and unmet needs. Their key therapy areas include those requiring specialized solutions due to licensing complexities or limited availability. Their product portfolio encompasses both pharmaceuticals and medical devices, including multi-layer decontamination antibacterial sticky mats used in operating theatres, ICUs, and laboratories worldwide. The company boasts GMP certifications and holds patents for their products, ensuring high quality and regulatory compliance. They have a strong distribution network spanning over 60 countries and a proven track record of success since 2004.

protamine sulfate

Vials, injection 10 mg/ml - 5 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Turkey
GMP approvals
EU GMP
Comments
Dossier is not suitable for submission in the regulated markets like EU and UK
Manufacturer #2722
It originally entered the pharmaceutical industry in 1987, when it introduced blood derivative products to Europe and became the exclusive distributor for prominent European brands. Oncology, hematology, dermatology, radiology, rheumatology, immunology, and OTC products are the seven main therapeutic fields.

Manufacturer usually replies in 7 days

protamine sulfate

Vials, injection 50 mg/5 ml

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
EU GMP
Manufacturer #2303
A pharmaceutical manufacturer with over 25 years of experience that develops and produces fixed-dose and single-entity generic and specialty pharmaceutical products. The company offers an extensive range of injectable dosage forms, including parenterals, and also manufactures oral solids. Its facilities operate under recognised international quality certifications such as EU-GMP, ANVISA, PIC/S and TGA approvals, supporting reliable large-scale production of pharmaceutical products for global export while emphasizing efficacy, affordability and consistent quality.

Manufacturer usually replies in 20 days

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