SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 1Ace Japan Co., Ltd.
03 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia Probucol
02 1Japanese Pharmacopoeia probucol
03 1Probucol
01 2Japan
02 1Taiwan
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 229MF10022
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2017-01-31
Latest Date of Registration : 2017-01-31
Japanese Pharmacopoeia Probucol
Registration Number : 305MF10113
Registrant's Address : 5850-1 Higashine-ko, Higashine City, Yamagata Prefecture
Initial Date of Registration : 2023-10-04
Latest Date of Registration : 2023-10-04
Japanese Pharmacopoeia Probucol
Registration Number : 222MF10231
Registrant's Address : 2-27-1 Shinkawa, Chuo-ku, Tokyo
Initial Date of Registration : 2010-09-24
Latest Date of Registration : 2010-09-24
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PharmaCompass offers a list of Probucol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Probucol manufacturer or Probucol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Probucol manufacturer or Probucol supplier.
A Panavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Panavir, including repackagers and relabelers. The FDA regulates Panavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Panavir 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 Panavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Panavir supplier is an individual or a company that provides Panavir active pharmaceutical ingredient (API) or Panavir finished formulations upon request. The Panavir suppliers may include Panavir API manufacturers, exporters, distributors and traders.
click here to find a list of Panavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Panavir Drug Master File in Japan (Panavir JDMF) empowers Panavir 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 Panavir JDMF during the approval evaluation for pharmaceutical products. At the time of Panavir 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 Panavir suppliers with JDMF on PharmaCompass.
We have 3 companies offering Panavir
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