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