01 1Katwijk Chemie bv
01 1Japanese Pharmacopoeia outside pemoline (production only)
01 1Netherlands
Pemoline (for manufacturing purposes only), outside the Japanese Pharmacopoeia.
Registration Number : 219MF10057
Registrant's Address : Snijderstraat 6,2222 BA, Katwijk, ZH The Netherlands
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2016-02-08
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PharmaCompass offers a list of Pemoline 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 Pemoline manufacturer or Pemoline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pemoline manufacturer or Pemoline supplier.
PharmaCompass also assists you with knowing the Pemoline API Price utilized in the formulation of products. Pemoline API Price is not always fixed or binding as the Pemoline Price is obtained through a variety of data sources. The Pemoline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Centramin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Centramin, including repackagers and relabelers. The FDA regulates Centramin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Centramin 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 Centramin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Centramin supplier is an individual or a company that provides Centramin active pharmaceutical ingredient (API) or Centramin finished formulations upon request. The Centramin suppliers may include Centramin API manufacturers, exporters, distributors and traders.
click here to find a list of Centramin 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 Centramin Drug Master File in Japan (Centramin JDMF) empowers Centramin 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 Centramin JDMF during the approval evaluation for pharmaceutical products. At the time of Centramin 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 Centramin suppliers with JDMF on PharmaCompass.
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