01 1Sun Chemical Co., Ltd.
01 1Procainamide hydrochloride
01 1China
Registration Number : 218MF10970
Registrant's Address : 29-3 Shinmachi, Yashio City, Saitama Prefecture
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2006-12-01
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PharmaCompass offers a list of Procainamide Hydrochloride 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 Procainamide Hydrochloride manufacturer or Procainamide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procainamide Hydrochloride manufacturer or Procainamide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Procainamide Hydrochloride API Price utilized in the formulation of products. Procainamide Hydrochloride API Price is not always fixed or binding as the Procainamide Hydrochloride Price is obtained through a variety of data sources. The Procainamide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biocoryl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biocoryl, including repackagers and relabelers. The FDA regulates Biocoryl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biocoryl 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 Biocoryl supplier is an individual or a company that provides Biocoryl active pharmaceutical ingredient (API) or Biocoryl finished formulations upon request. The Biocoryl suppliers may include Biocoryl 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 Biocoryl Drug Master File in Japan (Biocoryl JDMF) empowers Biocoryl 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 Biocoryl JDMF during the approval evaluation for pharmaceutical products. At the time of Biocoryl 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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