01 1C S Bio Co.
02 1Peptisyntha, Inc.
01 2Oxytocin
01 1Germany
02 1U.S.A
Registration Number : 222MF10157
Registrant's Address : 20901 Higgins Court Torrance, California USA 90501-1722
Initial Date of Registration : 2010-05-24
Latest Date of Registration : 2010-05-24
Registration Number : 226MF10086
Registrant's Address : ２０ Ｋｅｌｌｙ Ｃｏｕｒｔ，Ｍｅｎｌｏ Ｐａｒｋ，ＣＡ...
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2023-09-20
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PharmaCompass offers a list of Oxytocin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Oxytocin manufacturer or Oxytocin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxytocin manufacturer or Oxytocin supplier.
A Posterior pituitary extract manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Posterior pituitary extract, including repackagers and relabelers. The FDA regulates Posterior pituitary extract manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Posterior pituitary extract 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 Posterior pituitary extract manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Posterior pituitary extract supplier is an individual or a company that provides Posterior pituitary extract active pharmaceutical ingredient (API) or Posterior pituitary extract finished formulations upon request. The Posterior pituitary extract suppliers may include Posterior pituitary extract API manufacturers, exporters, distributors and traders.
click here to find a list of Posterior pituitary extract suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Posterior pituitary extract Drug Master File in Japan (Posterior pituitary extract JDMF) empowers Posterior pituitary extract 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 Posterior pituitary extract JDMF during the approval evaluation for pharmaceutical products. At the time of Posterior pituitary extract 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 Posterior pituitary extract suppliers with JDMF on PharmaCompass.
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