01 1Harman Finochem Ltd.
01 1Succinylcholine Chloride
01 1India
Registration Number : 304MF10080
Registrant's Address : 107-A, Vinay Bhavya Complex, 159-A, C. S. T Road, Kalina, Santa Cruz (East), Mumbai-4...
Initial Date of Registration : 2022-05-25
Latest Date of Registration : 2022-05-25
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PharmaCompass offers a list of Succinylcholine Chloride 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 Succinylcholine Chloride manufacturer or Succinylcholine Chloride supplier for your needs.
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PharmaCompass also assists you with knowing the Succinylcholine Chloride API Price utilized in the formulation of products. Succinylcholine Chloride API Price is not always fixed or binding as the Succinylcholine Chloride Price is obtained through a variety of data sources. The Succinylcholine Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cloruro de suxametonio manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloruro de suxametonio, including repackagers and relabelers. The FDA regulates Cloruro de suxametonio manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloruro de suxametonio API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Cloruro de suxametonio supplier is an individual or a company that provides Cloruro de suxametonio active pharmaceutical ingredient (API) or Cloruro de suxametonio finished formulations upon request. The Cloruro de suxametonio suppliers may include Cloruro de suxametonio API manufacturers, exporters, distributors and traders.
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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 Cloruro de suxametonio Drug Master File in Japan (Cloruro de suxametonio JDMF) empowers Cloruro de suxametonio 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 Cloruro de suxametonio JDMF during the approval evaluation for pharmaceutical products. At the time of Cloruro de suxametonio 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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