01 1Flamma S. p. A.
01 1Methacholine Chloride
01 1Italy
Registration Number : 304MF10146
Registrant's Address : Via Bedeschi, 22 24040 Chignolo d'Isola (Bergamo) Italy
Initial Date of Registration : 2022-11-02
Latest Date of Registration : 2022-11-02
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PharmaCompass offers a list of Methacholine 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 Methacholine Chloride manufacturer or Methacholine Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methacholine Chloride manufacturer or Methacholine Chloride supplier.
PharmaCompass also assists you with knowing the Methacholine Chloride API Price utilized in the formulation of products. Methacholine Chloride API Price is not always fixed or binding as the Methacholine Chloride Price is obtained through a variety of data sources. The Methacholine Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metacolina cloruro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metacolina cloruro, including repackagers and relabelers. The FDA regulates Metacolina cloruro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metacolina cloruro API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Metacolina cloruro supplier is an individual or a company that provides Metacolina cloruro active pharmaceutical ingredient (API) or Metacolina cloruro finished formulations upon request. The Metacolina cloruro suppliers may include Metacolina cloruro 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 Metacolina cloruro Drug Master File in Japan (Metacolina cloruro JDMF) empowers Metacolina cloruro 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 Metacolina cloruro JDMF during the approval evaluation for pharmaceutical products. At the time of Metacolina cloruro 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 Metacolina cloruro suppliers with JDMF on PharmaCompass.
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