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 Disodium Pamidronate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disodium Pamidronate, including repackagers and relabelers. The FDA regulates Disodium Pamidronate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disodium Pamidronate 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 Disodium Pamidronate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disodium Pamidronate supplier is an individual or a company that provides Disodium Pamidronate active pharmaceutical ingredient (API) or Disodium Pamidronate finished formulations upon request. The Disodium Pamidronate suppliers may include Disodium Pamidronate API manufacturers, exporters, distributors and traders.
click here to find a list of Disodium Pamidronate 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 Disodium Pamidronate Drug Master File in Japan (Disodium Pamidronate JDMF) empowers Disodium Pamidronate 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 Disodium Pamidronate JDMF during the approval evaluation for pharmaceutical products. At the time of Disodium Pamidronate 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 Disodium Pamidronate suppliers with JDMF on PharmaCompass.
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