Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Rexim (Nanning) Pharmaceutical Co. , Ltd.
02 1SHANGHAI PLUMINO AMINO ACID CO. , LTD.
03 1SHINE STAR (HUBEI) BIOLOGICAL ENGINEERING CO. , LTD.
01 1Japanese Pharmacopoeia L- valine (production only)
02 1L- valine L-Valine
03 1L-VALINE
01 1China
02 1Germany
03 1Blank
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 228MF10022
Registrant's Address : No. 46 Wenjiang Road, Wuming District, Nanning, 530199, Guangxi, P. R. China
Initial Date of Registration : 2016-02-02
Latest Date of Registration : 2019-06-18
Registration Number : 305MF10089
Registrant's Address : No. 666 Chanling Avenue, Douhudi Town, Gong An, Jingzhou, Hubei, P. R. China
Initial Date of Registration : 2023-07-26
Latest Date of Registration : 2023-07-26
Japanese Pharmacopoeia L-valine (for manufacturing purposes only)
Registration Number : 229MF10081
Registrant's Address : No. 158, Xintuan Road, Qingpu Industrial Zone, Shanghai, CHINA ZIP 201707
Initial Date of Registration : 2017-04-11
Latest Date of Registration : 2017-04-11
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PharmaCompass offers a list of L-VALINE 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 L-VALINE manufacturer or L-VALINE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-VALINE manufacturer or L-VALINE supplier.
PharmaCompass also assists you with knowing the L-VALINE API Price utilized in the formulation of products. L-VALINE API Price is not always fixed or binding as the L-VALINE Price is obtained through a variety of data sources. The L-VALINE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BD34735 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BD34735, including repackagers and relabelers. The FDA regulates BD34735 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BD34735 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 BD34735 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BD34735 supplier is an individual or a company that provides BD34735 active pharmaceutical ingredient (API) or BD34735 finished formulations upon request. The BD34735 suppliers may include BD34735 API manufacturers, exporters, distributors and traders.
click here to find a list of BD34735 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 BD34735 Drug Master File in Japan (BD34735 JDMF) empowers BD34735 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 BD34735 JDMF during the approval evaluation for pharmaceutical products. At the time of BD34735 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 BD34735 suppliers with JDMF on PharmaCompass.
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