01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Cysteamine Hydrochloride
01 1Italy
Registration Number : 305MF10060
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2023-05-17
Latest Date of Registration : 2024-02-07
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PharmaCompass offers a list of Cysteamine 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 Cysteamine Hydrochloride manufacturer or Cysteamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cysteamine Hydrochloride manufacturer or Cysteamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cysteamine Hydrochloride API Price utilized in the formulation of products. Cysteamine Hydrochloride API Price is not always fixed or binding as the Cysteamine Hydrochloride Price is obtained through a variety of data sources. The Cysteamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cysteamine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cysteamine HCl, including repackagers and relabelers. The FDA regulates Cysteamine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cysteamine HCl 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 Cysteamine HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cysteamine HCl supplier is an individual or a company that provides Cysteamine HCl active pharmaceutical ingredient (API) or Cysteamine HCl finished formulations upon request. The Cysteamine HCl suppliers may include Cysteamine HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Cysteamine HCl 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 Cysteamine HCl Drug Master File in Japan (Cysteamine HCl JDMF) empowers Cysteamine HCl 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 Cysteamine HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Cysteamine HCl 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 Cysteamine HCl suppliers with JDMF on PharmaCompass.
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