01 1Kaiping Genuine Biochemical Pharmaceutical Co. , Ltd.
01 1Adenosine Triphosphate Disodium
01 1China
Adenosine Triphosphate Disodium
Registration Number : 304MF10073
Registrant's Address : No. 1 Xinke Road, Biaohai Industrial Park, Shatang Town, Kaiping City, Guangdong
Initial Date of Registration : 2022-05-18
Latest Date of Registration : 2022-05-18
A Adenosine Triphosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adenosine Triphosphate, including repackagers and relabelers. The FDA regulates Adenosine Triphosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adenosine Triphosphate 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 Adenosine Triphosphate supplier is an individual or a company that provides Adenosine Triphosphate active pharmaceutical ingredient (API) or Adenosine Triphosphate finished formulations upon request. The Adenosine Triphosphate suppliers may include Adenosine Triphosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Adenosine Triphosphate 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 Adenosine Triphosphate Drug Master File in Japan (Adenosine Triphosphate JDMF) empowers Adenosine Triphosphate 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 Adenosine Triphosphate JDMF during the approval evaluation for pharmaceutical products. At the time of Adenosine Triphosphate 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 Adenosine Triphosphate suppliers with JDMF on PharmaCompass.
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