Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works POLPHARMA S. A.
02 1Excella GmbH & Co. K.G.
01 2Baclofen
01 1Luxembourg
02 1Poland
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 230MF10014
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2018-01-30
Latest Date of Registration : 2019-03-19
Registration Number : 220MF10253
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2008-12-12
Latest Date of Registration : 2008-12-12
39
PharmaCompass offers a list of Baclofen API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Baclofen manufacturer or Baclofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Baclofen manufacturer or Baclofen supplier.
PharmaCompass also assists you with knowing the Baclofen API Price utilized in the formulation of products. Baclofen API Price is not always fixed or binding as the Baclofen Price is obtained through a variety of data sources. The Baclofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lioresal, Liofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lioresal, Liofen, including repackagers and relabelers. The FDA regulates Lioresal, Liofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lioresal, Liofen 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 Lioresal, Liofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lioresal, Liofen supplier is an individual or a company that provides Lioresal, Liofen active pharmaceutical ingredient (API) or Lioresal, Liofen finished formulations upon request. The Lioresal, Liofen suppliers may include Lioresal, Liofen API manufacturers, exporters, distributors and traders.
click here to find a list of Lioresal, Liofen 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 Lioresal, Liofen Drug Master File in Japan (Lioresal, Liofen JDMF) empowers Lioresal, Liofen 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 Lioresal, Liofen JDMF during the approval evaluation for pharmaceutical products. At the time of Lioresal, Liofen 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 Lioresal, Liofen suppliers with JDMF on PharmaCompass.
