CSBio provides high-quality custom peptides, cGMP peptides, automated peptide synthesizers & other instrumentation to biotech industry.
01 1C.S. Bio Co.
02 1Peptisyntha, Inc.
01 2Oxytocin
01 1Germany
02 1U.S.A
CSBio provides high-quality custom peptides, cGMP peptides, automated peptide synthesizers & other instrumentation to biotech industry.
Registration Number : 226MF10086
Registrant's Address : 20 Kelly Court, Menlo Park, CA 94025 USA
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2023-09-20
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
A Oxytocin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytocin Acetate, including repackagers and relabelers. The FDA regulates Oxytocin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytocin Acetate 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 Oxytocin Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytocin Acetate supplier is an individual or a company that provides Oxytocin Acetate active pharmaceutical ingredient (API) or Oxytocin Acetate finished formulations upon request. The Oxytocin Acetate suppliers may include Oxytocin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytocin Acetate 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 Oxytocin Acetate Drug Master File in Japan (Oxytocin Acetate JDMF) empowers Oxytocin Acetate 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 Oxytocin Acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Oxytocin Acetate 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 Oxytocin Acetate suppliers with JDMF on PharmaCompass.
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