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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sirolimus manufacturer or Sirolimus supplier.
PharmaCompass also assists you with knowing the Sirolimus API Price utilized in the formulation of products. Sirolimus API Price is not always fixed or binding as the Sirolimus Price is obtained through a variety of data sources. The Sirolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RAP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RAP, including repackagers and relabelers. The FDA regulates RAP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RAP 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 RAP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RAP supplier is an individual or a company that provides RAP active pharmaceutical ingredient (API) or RAP finished formulations upon request. The RAP suppliers may include RAP API manufacturers, exporters, distributors and traders.
click here to find a list of RAP 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 RAP Drug Master File in Japan (RAP JDMF) empowers RAP 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 RAP JDMF during the approval evaluation for pharmaceutical products. At the time of RAP 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 RAP suppliers with JDMF on PharmaCompass.
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