Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA S. L.
02 1Chengdu Easton Biopharmaceuticals Co. , Ltd.
03 1Arevipharma GmbH
04 2Daito Co., Ltd.
05 1MERCK&CIE KG
06 1Merck & Cie KmG
07 1Permachem Asia Co., Ltd.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 218MF10893
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2019-09-11
Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.
Registration Number : 230MF10053
Registrant's Address : No. 8, Xiyuan Avenue, Hi-Tech District, Chengdu, 611731, China.
Initial Date of Registration : 2018-04-17
Latest Date of Registration : 2018-04-17
37
PharmaCompass offers a list of Bisoprolol Fumarate 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 Bisoprolol Fumarate manufacturer or Bisoprolol Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bisoprolol Fumarate manufacturer or Bisoprolol Fumarate supplier.
PharmaCompass also assists you with knowing the Bisoprolol Fumarate API Price utilized in the formulation of products. Bisoprolol Fumarate API Price is not always fixed or binding as the Bisoprolol Fumarate Price is obtained through a variety of data sources. The Bisoprolol Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ZIAC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZIAC, including repackagers and relabelers. The FDA regulates ZIAC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZIAC 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 ZIAC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ZIAC supplier is an individual or a company that provides ZIAC active pharmaceutical ingredient (API) or ZIAC finished formulations upon request. The ZIAC suppliers may include ZIAC API manufacturers, exporters, distributors and traders.
click here to find a list of ZIAC 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 ZIAC Drug Master File in Japan (ZIAC JDMF) empowers ZIAC 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 ZIAC JDMF during the approval evaluation for pharmaceutical products. At the time of ZIAC 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 ZIAC suppliers with JDMF on PharmaCompass.
We have 6 companies offering ZIAC
Get in contact with the supplier of your choice:
