01 1Qingdao Kangyuan Pharmaceutical Co. , Ltd.
02 3Shanghai Tianwei Biopharmaceutical Co., Ltd.
03 3Watahan Trading Co., Ltd.
01 1Chorionic gonadotropin
02 2Day stations
03 1Human Chorionic Gonadotropin
04 1Outsider regulations purified pituitary gonadotropin
05 1Pituitary gonadotropin (manufactured only)
06 1Purification pituitary gonadotropin (manufactured only)
01 4China
02 3Japan
Registration Number : 306MF10041
Registrant's Address : Yinghai Industrial Park, Jiaozhou City 266300, Qingdao, Shandong Province, China
Initial Date of Registration : 2024-03-13
Latest Date of Registration : 2024-03-13
Japanese Pharmacopoeia "Human Chorionic Gonadotropin"
Registration Number : 219MF10213
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2007-06-25
Latest Date of Registration : 2017-06-21
Japanese Pharmacopoeia "Human Pituitary Gonadotropin"
Registration Number : 218MF10925
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2006-11-21
Latest Date of Registration : 2017-06-21
Purified pituitary gonadotropin
Registration Number : 220MF10135
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2008-05-29
Latest Date of Registration : 2015-10-21
Pituitary gonadotropin (for manufacturing purposes only)
Registration Number : 217MF11262
Registrant's Address : 1-4 Yotsuya, Shinjuku-ku, Tokyo
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2017-10-30
Purified pituitary gonadotropin (for manufacturing purposes only)
Registration Number : 217MF11263
Registrant's Address : 1-4 Yotsuya, Shinjuku-ku, Tokyo
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2022-01-13
Placental gonadotropin "Mitsuba"
Registration Number : 217MF11261
Registrant's Address : 1-4 Yotsuya, Shinjuku-ku, Tokyo
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2017-06-29
53
PharmaCompass offers a list of Human Chorionic Gonadotropin 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 Human Chorionic Gonadotropin manufacturer or Human Chorionic Gonadotropin supplier for your needs.
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PharmaCompass also assists you with knowing the Human Chorionic Gonadotropin API Price utilized in the formulation of products. Human Chorionic Gonadotropin API Price is not always fixed or binding as the Human Chorionic Gonadotropin Price is obtained through a variety of data sources. The Human Chorionic Gonadotropin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A beta subunit HCG (123-145) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of beta subunit HCG (123-145), including repackagers and relabelers. The FDA regulates beta subunit HCG (123-145) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. beta subunit HCG (123-145) 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 beta subunit HCG (123-145) supplier is an individual or a company that provides beta subunit HCG (123-145) active pharmaceutical ingredient (API) or beta subunit HCG (123-145) finished formulations upon request. The beta subunit HCG (123-145) suppliers may include beta subunit HCG (123-145) API manufacturers, exporters, distributors and traders.
click here to find a list of beta subunit HCG (123-145) 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 beta subunit HCG (123-145) Drug Master File in Japan (beta subunit HCG (123-145) JDMF) empowers beta subunit HCG (123-145) 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 beta subunit HCG (123-145) JDMF during the approval evaluation for pharmaceutical products. At the time of beta subunit HCG (123-145) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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