01 1Heraeus Precious Metals GmbH & Co. K.G.
01 1Thiotepa
01 1Germany
Registration Number : 229MF10141
Registrant's Address : Heraeusstr. 12-14;63450 Hanau;Germany
Initial Date of Registration : 2017-07-25
Latest Date of Registration : 2025-05-21
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PharmaCompass offers a list of Thiotepa 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 Thiotepa manufacturer or Thiotepa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Thiotepa manufacturer or Thiotepa supplier.
PharmaCompass also assists you with knowing the Thiotepa API Price utilized in the formulation of products. Thiotepa API Price is not always fixed or binding as the Thiotepa Price is obtained through a variety of data sources. The Thiotepa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C07641 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07641, including repackagers and relabelers. The FDA regulates C07641 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07641 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 C07641 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C07641 supplier is an individual or a company that provides C07641 active pharmaceutical ingredient (API) or C07641 finished formulations upon request. The C07641 suppliers may include C07641 API manufacturers, exporters, distributors and traders.
click here to find a list of C07641 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 C07641 Drug Master File in Japan (C07641 JDMF) empowers C07641 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 C07641 JDMF during the approval evaluation for pharmaceutical products. At the time of C07641 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 C07641 suppliers with JDMF on PharmaCompass.
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