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 : 2025-10-15
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A Triethylenethiophosphoramide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triethylenethiophosphoramide, including repackagers and relabelers. The FDA regulates Triethylenethiophosphoramide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triethylenethiophosphoramide 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 Triethylenethiophosphoramide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Triethylenethiophosphoramide supplier is an individual or a company that provides Triethylenethiophosphoramide active pharmaceutical ingredient (API) or Triethylenethiophosphoramide finished formulations upon request. The Triethylenethiophosphoramide suppliers may include Triethylenethiophosphoramide API manufacturers, exporters, distributors and traders.
click here to find a list of Triethylenethiophosphoramide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Triethylenethiophosphoramide Drug Master File in Japan (Triethylenethiophosphoramide JDMF) empowers Triethylenethiophosphoramide 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 Triethylenethiophosphoramide JDMF during the approval evaluation for pharmaceutical products. At the time of Triethylenethiophosphoramide 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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