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01 Heraeus Precious Metals GmbH & Co. K.G. (1)
01 Thiotepa (1)
01 Germany (1)
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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 MolPort-001-783-551 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-783-551, including repackagers and relabelers. The FDA regulates MolPort-001-783-551 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-783-551 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 MolPort-001-783-551 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-783-551 supplier is an individual or a company that provides MolPort-001-783-551 active pharmaceutical ingredient (API) or MolPort-001-783-551 finished formulations upon request. The MolPort-001-783-551 suppliers may include MolPort-001-783-551 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-783-551 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 MolPort-001-783-551 Drug Master File in Japan (MolPort-001-783-551 JDMF) empowers MolPort-001-783-551 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 MolPort-001-783-551 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-783-551 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 MolPort-001-783-551 suppliers with JDMF on PharmaCompass.
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