Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
01 1Laboratory Ofichem B. V.
01 1PAMIDRONATE DISODIUM PENTAHYDRATE
01 1Netherlands
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
PAMIDRONATE DISODIUM PENTAHYDRATE
Registration Number : 228MF10223
Registrant's Address : Heembadweg 5, 9561 CZ Ter apel, The Netherlands
Initial Date of Registration : 2016-11-25
Latest Date of Registration : 2024-10-31
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PharmaCompass offers a list of Pamidronate 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 Pamidronate manufacturer or Pamidronate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pamidronate manufacturer or Pamidronate supplier.
PharmaCompass also assists you with knowing the Pamidronate API Price utilized in the formulation of products. Pamidronate API Price is not always fixed or binding as the Pamidronate Price is obtained through a variety of data sources. The Pamidronate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A APD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of APD, including repackagers and relabelers. The FDA regulates APD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. APD 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 APD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A APD supplier is an individual or a company that provides APD active pharmaceutical ingredient (API) or APD finished formulations upon request. The APD suppliers may include APD API manufacturers, exporters, distributors and traders.
click here to find a list of APD 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 APD Drug Master File in Japan (APD JDMF) empowers APD 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 APD JDMF during the approval evaluation for pharmaceutical products. At the time of APD 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 APD suppliers with JDMF on PharmaCompass.
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