01 1SIGMA-ALDRICH ISRAEL Ltd.
01 1Dactinomycin USP
01 1U.S.A
Registration Number : 221MF10187
Registrant's Address : 13 Kiryat Mada Street, Har Hotzvim Industrial Park Jerusalem, 97770 ISRAEL
Initial Date of Registration : 2009-08-13
Latest Date of Registration : 2017-02-13
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PharmaCompass offers a list of Dactinomycin 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 Dactinomycin manufacturer or Dactinomycin supplier for your needs.
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PharmaCompass also assists you with knowing the Dactinomycin API Price utilized in the formulation of products. Dactinomycin API Price is not always fixed or binding as the Dactinomycin Price is obtained through a variety of data sources. The Dactinomycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA, including repackagers and relabelers. The FDA regulates PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA 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 PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA supplier is an individual or a company that provides PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA active pharmaceutical ingredient (API) or PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA finished formulations upon request. The PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA suppliers may include PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA API manufacturers, exporters, distributors and traders.
click here to find a list of PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA 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 PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA Drug Master File in Japan (PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA JDMF) empowers PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA 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 PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA JDMF during the approval evaluation for pharmaceutical products. At the time of PXZ-THR-DVA-PRO-SAR-MVA-THR-DVA-PRO-SAR-MVA JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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