01 1National Center for Nuclear Research
01 1Strontium nitrate (90Sr) solution
01 1Poland
Strontium nitrate (90Sr) solution
Registration Number : 218MF10542
Registrant's Address : Andrzej Soltan 7,05-400 Otwock, Poland
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2008-02-08
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PharmaCompass offers a list of Strontium Nitrate 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 Strontium Nitrate manufacturer or Strontium Nitrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Strontium Nitrate manufacturer or Strontium Nitrate supplier.
PharmaCompass also assists you with knowing the Strontium Nitrate API Price utilized in the formulation of products. Strontium Nitrate API Price is not always fixed or binding as the Strontium Nitrate Price is obtained through a variety of data sources. The Strontium Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A V0373 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of V0373, including repackagers and relabelers. The FDA regulates V0373 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. V0373 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A V0373 supplier is an individual or a company that provides V0373 active pharmaceutical ingredient (API) or V0373 finished formulations upon request. The V0373 suppliers may include V0373 API manufacturers, exporters, distributors and traders.
click here to find a list of V0373 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 V0373 Drug Master File in Japan (V0373 JDMF) empowers V0373 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 V0373 JDMF during the approval evaluation for pharmaceutical products. At the time of V0373 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 V0373 suppliers with JDMF on PharmaCompass.
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