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01 1EUROAPI Hungary Ltd.
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01 1Dinoprost
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01 1France
Registration Number : 221MF10190
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2009-08-18
Latest Date of Registration : 2009-08-18
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PharmaCompass offers a list of Dinoprost 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 Dinoprost manufacturer or Dinoprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dinoprost manufacturer or Dinoprost supplier.
PharmaCompass also assists you with knowing the Dinoprost API Price utilized in the formulation of products. Dinoprost API Price is not always fixed or binding as the Dinoprost Price is obtained through a variety of data sources. The Dinoprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A alpha, PGF2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of alpha, PGF2, including repackagers and relabelers. The FDA regulates alpha, PGF2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. alpha, PGF2 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 alpha, PGF2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A alpha, PGF2 supplier is an individual or a company that provides alpha, PGF2 active pharmaceutical ingredient (API) or alpha, PGF2 finished formulations upon request. The alpha, PGF2 suppliers may include alpha, PGF2 API manufacturers, exporters, distributors and traders.
click here to find a list of alpha, PGF2 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 alpha, PGF2 Drug Master File in Japan (alpha, PGF2 JDMF) empowers alpha, PGF2 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 alpha, PGF2 JDMF during the approval evaluation for pharmaceutical products. At the time of alpha, PGF2 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 alpha, PGF2 suppliers with JDMF on PharmaCompass.