01 1Dojin Pharmaceutical Chemical Co., Ltd.
02 1Sicor de Me(´)xico,S. A. de C. V.
01 1Deployed Don propionate "Teva"
02 1Deprodone propionic acid
01 1Japan
02 1Mexico
Registration Number : 217MF10385
Registrant's Address : Fukushima Prefecture, Fukushima City, Segami Town, Higashi Nakagawara 8-1
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2011-12-09
Registration Number : 218MF10927
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2006-11-21
A 3-5-Diiodothyropropionic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 3-5-Diiodothyropropionic Acid, including repackagers and relabelers. The FDA regulates 3-5-Diiodothyropropionic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 3-5-Diiodothyropropionic Acid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 3-5-Diiodothyropropionic Acid supplier is an individual or a company that provides 3-5-Diiodothyropropionic Acid active pharmaceutical ingredient (API) or 3-5-Diiodothyropropionic Acid finished formulations upon request. The 3-5-Diiodothyropropionic Acid suppliers may include 3-5-Diiodothyropropionic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of 3-5-Diiodothyropropionic Acid 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 3-5-Diiodothyropropionic Acid Drug Master File in Japan (3-5-Diiodothyropropionic Acid JDMF) empowers 3-5-Diiodothyropropionic Acid 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 3-5-Diiodothyropropionic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of 3-5-Diiodothyropropionic Acid 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 3-5-Diiodothyropropionic Acid suppliers with JDMF on PharmaCompass.
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