Inke S.A: APIs manufacturing plant.
01 1Inke S.A.
02 1Wavelength Enterprises Ltd
03 1Chungking Carelife Pharmaceutical Co., Ltd.
04 1Hamari PFST Co., Ltd.
05 1Hamari Pharmaceuticals Co., Ltd.
06 2Hana Pharmaceutical Co. , Ltd.
07 1Hubei Haosun Pharmaceutical Co. , Ltd.
08 1Natco Pharma Limited.
09 2Qilu Pharmaceutical Co. , Ltd.
Inke S.A: APIs manufacturing plant.
Registration Number : 218MF10350
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-12-01
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Registration Number : 218MF10399
Registrant's Address : 29 Lehi St. , Bnei-Brak 5120050, P. O. Box 2231 Israel
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2006-11-15
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PharmaCompass offers a list of Granisetron Hydrochloride 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 Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier.
PharmaCompass also assists you with knowing the Granisetron Hydrochloride API Price utilized in the formulation of products. Granisetron Hydrochloride API Price is not always fixed or binding as the Granisetron Hydrochloride Price is obtained through a variety of data sources. The Granisetron Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A GRANISOL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of GRANISOL, including repackagers and relabelers. The FDA regulates GRANISOL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. GRANISOL 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 GRANISOL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A GRANISOL supplier is an individual or a company that provides GRANISOL active pharmaceutical ingredient (API) or GRANISOL finished formulations upon request. The GRANISOL suppliers may include GRANISOL API manufacturers, exporters, distributors and traders.
click here to find a list of GRANISOL 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 GRANISOL Drug Master File in Japan (GRANISOL JDMF) empowers GRANISOL 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 GRANISOL JDMF during the approval evaluation for pharmaceutical products. At the time of GRANISOL 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 GRANISOL suppliers with JDMF on PharmaCompass.
We have 9 companies offering GRANISOL
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