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 1TAPI Czech Industries s. r. o.
03 1Astellas Pharma Inc.
04 1CERES F&D Inc.
05 1CKD Bio Corporation
06 1CONCORD BIOTECH LIMITED.
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01 1Prograf
02 2Tacrolimus
03 1Tacrolimus hydrate
04 1Tacrolimus hydrate "Teva"
05 1Tacrolimus hydrate (production only)
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01 1India
02 1Israel
03 1Japan
04 2South Korea
05 1Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 224MF10125
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2012-07-13
Latest Date of Registration : 2013-05-20
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 222MF10265
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2010-12-08
Latest Date of Registration : 2015-12-11
Registration Number : 217MF11288
Registrant's Address : 2-5-1 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2007-09-10
Registration Number : 302MF10106
Registrant's Address : 100, Bio Valley 2-ro, Jecheon-si, Chungcheongbuk-do, 27159, Republic of Korea
Initial Date of Registration : 2020-09-01
Latest Date of Registration : 2020-09-01
Registration Number : 306MF10114
Registrant's Address : 8, Chungjeong-ro, Seodaemun-gu, Seoul, Republic of Korea
Initial Date of Registration : 2024-08-22
Latest Date of Registration : 2024-08-22
Tacrolimus hydrate (for manufacturing only)
Registration Number : 222MF10197
Registrant's Address : 1482-1486, Trasad Road, Dholka, Dist. Ahmedabad-382225, Gujarat, INDIA
Initial Date of Registration : 2010-07-13
Latest Date of Registration : 2010-07-13
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A Ambap5429 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ambap5429, including repackagers and relabelers. The FDA regulates Ambap5429 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ambap5429 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 Ambap5429 supplier is an individual or a company that provides Ambap5429 active pharmaceutical ingredient (API) or Ambap5429 finished formulations upon request. The Ambap5429 suppliers may include Ambap5429 API manufacturers, exporters, distributors and traders.
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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 Ambap5429 Drug Master File in Japan (Ambap5429 JDMF) empowers Ambap5429 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 Ambap5429 JDMF during the approval evaluation for pharmaceutical products. At the time of Ambap5429 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 Ambap5429 suppliers with JDMF on PharmaCompass.
We have 6 companies offering Ambap5429
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