01 1Guangxi Nanning Baihui Pharmaceutical Group Nanning Bowbo Biological Engineering Co., Ltd.
01 1Bromelain L
01 1China
Registration Number : 220MF10157
Registrant's Address : Building D, Yinkai Industrial Park, Nanyan Line, Shajing Avenue, Nanning, China
Initial Date of Registration : 2008-06-30
Latest Date of Registration : 2008-06-30
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PharmaCompass offers a list of Bromelain 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 Bromelain manufacturer or Bromelain supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bromelain manufacturer or Bromelain supplier.
PharmaCompass also assists you with knowing the Bromelain API Price utilized in the formulation of products. Bromelain API Price is not always fixed or binding as the Bromelain Price is obtained through a variety of data sources. The Bromelain Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A bromelaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of bromelaine, including repackagers and relabelers. The FDA regulates bromelaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. bromelaine 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 bromelaine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A bromelaine supplier is an individual or a company that provides bromelaine active pharmaceutical ingredient (API) or bromelaine finished formulations upon request. The bromelaine suppliers may include bromelaine API manufacturers, exporters, distributors and traders.
click here to find a list of bromelaine 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 bromelaine Drug Master File in Japan (bromelaine JDMF) empowers bromelaine 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 bromelaine JDMF during the approval evaluation for pharmaceutical products. At the time of bromelaine 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 bromelaine suppliers with JDMF on PharmaCompass.
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