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PharmaCompass offers a list of DL-Valine API 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 DL-Valine API manufacturer or DL-Valine API supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred DL-Valine API manufacturer or DL-Valine API supplier.
PharmaCompass also assists you with knowing the DL-Valine API API Price utilized in the formulation of products. DL-Valine API API Price is not always fixed or binding as the DL-Valine API Price is obtained through a variety of data sources. The DL-Valine API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (dl)-valine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (dl)-valine, including repackagers and relabelers. The FDA regulates (dl)-valine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (dl)-valine 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 (dl)-valine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (dl)-valine supplier is an individual or a company that provides (dl)-valine active pharmaceutical ingredient (API) or (dl)-valine finished formulations upon request. The (dl)-valine suppliers may include (dl)-valine API manufacturers, exporters, distributors and traders.
click here to find a list of (dl)-valine 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 (dl)-valine Drug Master File in Japan ((dl)-valine JDMF) empowers (dl)-valine 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 (dl)-valine JDMF during the approval evaluation for pharmaceutical products. At the time of (dl)-valine 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 (dl)-valine suppliers with JDMF on PharmaCompass.
We have 4 companies offering (dl)-valine
Get in contact with the supplier of your choice: