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
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PharmaCompass offers a list of Adenosine Triphosphate 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 Adenosine Triphosphate manufacturer or Adenosine Triphosphate supplier for your needs.
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PharmaCompass also assists you with knowing the Adenosine Triphosphate API Price utilized in the formulation of products. Adenosine Triphosphate API Price is not always fixed or binding as the Adenosine Triphosphate Price is obtained through a variety of data sources. The Adenosine Triphosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 065A467 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 065A467, including repackagers and relabelers. The FDA regulates 065A467 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 065A467 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 065A467 supplier is an individual or a company that provides 065A467 active pharmaceutical ingredient (API) or 065A467 finished formulations upon request. The 065A467 suppliers may include 065A467 API manufacturers, exporters, distributors and traders.
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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 065A467 Drug Master File in Japan (065A467 JDMF) empowers 065A467 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 065A467 JDMF during the approval evaluation for pharmaceutical products. At the time of 065A467 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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