Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
02 2TAPI Hungary Industries Ltd.
03 2Biocon Limited
04 2Guangdong Blue Treasure Pharmaceuticals Co. , Ltd.
05 1Kyowa Hakko Bio Co., Ltd.
06 2Shanghai Tianwei Biopharmaceutical Co., Ltd.
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 218MF10474
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2006-04-27
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 307MF10010
Registrant's Address : 13 Pallagi u(´)t, Debrecen, 4042-Hungary
Initial Date of Registration : 2025-01-09
Latest Date of Registration : 2025-01-09
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 218MF10727
Registrant's Address : 13 Pallagi u(´)t, Debrecen, 4042-Hungary
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2015-12-15
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PharmaCompass offers a list of Pravastatin 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 Pravastatin manufacturer or Pravastatin supplier for your needs.
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PharmaCompass also assists you with knowing the Pravastatin API Price utilized in the formulation of products. Pravastatin API Price is not always fixed or binding as the Pravastatin Price is obtained through a variety of data sources. The Pravastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aplactin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aplactin, including repackagers and relabelers. The FDA regulates Aplactin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aplactin 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 Aplactin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aplactin supplier is an individual or a company that provides Aplactin active pharmaceutical ingredient (API) or Aplactin finished formulations upon request. The Aplactin suppliers may include Aplactin API manufacturers, exporters, distributors and traders.
click here to find a list of Aplactin 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 Aplactin Drug Master File in Japan (Aplactin JDMF) empowers Aplactin 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 Aplactin JDMF during the approval evaluation for pharmaceutical products. At the time of Aplactin 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 Aplactin suppliers with JDMF on PharmaCompass.
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