Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania S. A.
02 1TAPI Czech Industries s. r. o.
03 2Chongqing Pharmaceutical Research Institute Co. , Ltd.
04 1Jiangsu Hansoh Pharmaceutical Group Co. , Ltd.
05 1Nippon Kayaku Co., Ltd.
06 1Samyang Biopharmaceuticals Corporation
07 1Samyang Holdings Corporation
08 1Shandong Anhong Pharmaceutical Co. , Ltd.
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Pemetrexed sodium hemipentahydrate
Registration Number : 227MF10035
Registrant's Address : Balmes 85, Atico, 08008 (Barcelona), Spain
Initial Date of Registration : 2015-02-04
Latest Date of Registration : 2015-02-04
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Pemetrexed sodium hydrate "Teva"
Registration Number : 227MF10067
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2015-03-06
Latest Date of Registration : 2020-11-09
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PharmaCompass offers a list of Pemetrexed Disodium 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 Pemetrexed Disodium manufacturer or Pemetrexed Disodium supplier for your needs.
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PharmaCompass also assists you with knowing the Pemetrexed Disodium API Price utilized in the formulation of products. Pemetrexed Disodium API Price is not always fixed or binding as the Pemetrexed Disodium Price is obtained through a variety of data sources. The Pemetrexed Disodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pemetrexed Disodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pemetrexed Disodium, including repackagers and relabelers. The FDA regulates Pemetrexed Disodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pemetrexed Disodium 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 Pemetrexed Disodium supplier is an individual or a company that provides Pemetrexed Disodium active pharmaceutical ingredient (API) or Pemetrexed Disodium finished formulations upon request. The Pemetrexed Disodium suppliers may include Pemetrexed Disodium API manufacturers, exporters, distributors and traders.
click here to find a list of Pemetrexed Disodium 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 Pemetrexed Disodium Drug Master File in Japan (Pemetrexed Disodium JDMF) empowers Pemetrexed Disodium 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 Pemetrexed Disodium JDMF during the approval evaluation for pharmaceutical products. At the time of Pemetrexed Disodium 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 Pemetrexed Disodium suppliers with JDMF on PharmaCompass.
We have 7 companies offering Pemetrexed Disodium
Get in contact with the supplier of your choice:
