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