Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim S. A.
02 1Pharmaceutical Works POLPHARMA S. A.
03 1Glenmark Life Sciences Limited
04 1Honor Lab Limited
05 1Ryoto Fine Co., Ltd.
06 1SMS Pharmaceuticals Limited
07 1Tianish Laboratories Private Limited
08 1Topharman Shandong Co. ,Ltd
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Registration Number : 230MF10089
Registrant's Address : Joan Buscala, 10 E-08173 Sant Cugat del Valles, Barcelona, Spain
Initial Date of Registration : 2018-07-20
Latest Date of Registration : 2018-07-20
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 302MF10011
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2020-01-24
Latest Date of Registration : 2024-06-06
A Tadalafil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tadalafil, including repackagers and relabelers. The FDA regulates Tadalafil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tadalafil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tadalafil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tadalafil supplier is an individual or a company that provides Tadalafil active pharmaceutical ingredient (API) or Tadalafil finished formulations upon request. The Tadalafil suppliers may include Tadalafil API manufacturers, exporters, distributors and traders.
click here to find a list of Tadalafil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Tadalafil Drug Master File in Japan (Tadalafil JDMF) empowers Tadalafil API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Tadalafil JDMF during the approval evaluation for pharmaceutical products. At the time of Tadalafil JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Tadalafil suppliers with JDMF on PharmaCompass.
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