01 1Amano Enzyme Co., Ltd.
01 1Cellulase AP3
01 1United Kingdom
Registration Number : 217MF10463
Registrant's Address : 2-7 Nishiki 1-chome, Naka-ku, Nagoya City, Aichi Prefecture
Initial Date of Registration : 2005-08-24
Latest Date of Registration : 2006-11-06
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PharmaCompass offers a list of Cellulase 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 Cellulase manufacturer or Cellulase supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cellulase manufacturer or Cellulase supplier.
PharmaCompass also assists you with knowing the Cellulase API Price utilized in the formulation of products. Cellulase API Price is not always fixed or binding as the Cellulase Price is obtained through a variety of data sources. The Cellulase Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cellulase manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cellulase, including repackagers and relabelers. The FDA regulates Cellulase manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cellulase 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 Cellulase manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cellulase supplier is an individual or a company that provides Cellulase active pharmaceutical ingredient (API) or Cellulase finished formulations upon request. The Cellulase suppliers may include Cellulase API manufacturers, exporters, distributors and traders.
click here to find a list of Cellulase 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 Cellulase Drug Master File in Japan (Cellulase JDMF) empowers Cellulase 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 Cellulase JDMF during the approval evaluation for pharmaceutical products. At the time of Cellulase 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 Cellulase suppliers with JDMF on PharmaCompass.
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