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01 Kaiping Genuine Biochemical Pharmaceutical Co. , Ltd. (1)
01 Adenosine Triphosphate Disodium (1)
01 China (1)
64
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Adenosine Triphosphate manufacturer or Adenosine Triphosphate supplier.
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 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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