Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 2Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
02 1CONCORD BIOTECH LIMITED.
03 1Novo Nordisk Production Ireland Limited
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 303MF10065
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2021-04-13
Latest Date of Registration : 2024-10-02
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Rapamycin (for manufacturing purposes only)
Registration Number : 224MF10198
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2012-09-13
Latest Date of Registration : 2024-10-02
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PharmaCompass offers a list of Sirolimus 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 Sirolimus manufacturer or Sirolimus supplier for your needs.
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A DSSTox_CID_3582 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3582, including repackagers and relabelers. The FDA regulates DSSTox_CID_3582 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3582 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_CID_3582 supplier is an individual or a company that provides DSSTox_CID_3582 active pharmaceutical ingredient (API) or DSSTox_CID_3582 finished formulations upon request. The DSSTox_CID_3582 suppliers may include DSSTox_CID_3582 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3582 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 DSSTox_CID_3582 Drug Master File in Japan (DSSTox_CID_3582 JDMF) empowers DSSTox_CID_3582 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 DSSTox_CID_3582 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_3582 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 DSSTox_CID_3582 suppliers with JDMF on PharmaCompass.
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