Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
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01 1CHUNGHWA CHEMICAL SYNTHESIS & BIOTECH CO. , LTD.
02 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
03 1Ohara Pharmaceutical Co., Ltd.
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01 3Trandolapril
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01 1Japan
02 2Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 225MF10083
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2013-04-23
Latest Date of Registration : 2020-03-23
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 218MF10666
Registrant's Address : 1, Tung-Hsing, Street, Shu-Lin 238, Taipei Hsien, Taiwan, Republic of China
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
Registration Number : 217MF11216
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-12-01
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PharmaCompass offers a list of Trandolapril 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 Trandolapril manufacturer or Trandolapril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trandolapril manufacturer or Trandolapril supplier.
PharmaCompass also assists you with knowing the Trandolapril API Price utilized in the formulation of products. Trandolapril API Price is not always fixed or binding as the Trandolapril Price is obtained through a variety of data sources. The Trandolapril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Odrik manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Odrik, including repackagers and relabelers. The FDA regulates Odrik manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Odrik 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 Odrik manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Odrik supplier is an individual or a company that provides Odrik active pharmaceutical ingredient (API) or Odrik finished formulations upon request. The Odrik suppliers may include Odrik API manufacturers, exporters, distributors and traders.
click here to find a list of Odrik 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 Odrik Drug Master File in Japan (Odrik JDMF) empowers Odrik 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 Odrik JDMF during the approval evaluation for pharmaceutical products. At the time of Odrik 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 Odrik suppliers with JDMF on PharmaCompass.
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