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01 1Shandong Xinhua Pharmaceutical Co. , Ltd.
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01 1Pipemidic acid hydrate
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01 1China
Registration Number : 221MF10201
Registrant's Address : No. 14, Dongyi Road, Zhangdian Zibo, Shandong, P. R. China
Initial Date of Registration : 2009-09-14
Latest Date of Registration : 2009-09-14
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PharmaCompass offers a list of Piperidin-1-Yl-Acetic Acid 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 Piperidin-1-Yl-Acetic Acid manufacturer or Piperidin-1-Yl-Acetic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Piperidin-1-Yl-Acetic Acid API Price utilized in the formulation of products. Piperidin-1-Yl-Acetic Acid API Price is not always fixed or binding as the Piperidin-1-Yl-Acetic Acid Price is obtained through a variety of data sources. The Piperidin-1-Yl-Acetic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Piperidin-1-Yl-Acetic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Piperidin-1-Yl-Acetic Acid, including repackagers and relabelers. The FDA regulates Piperidin-1-Yl-Acetic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Piperidin-1-Yl-Acetic Acid 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 Piperidin-1-Yl-Acetic Acid supplier is an individual or a company that provides Piperidin-1-Yl-Acetic Acid active pharmaceutical ingredient (API) or Piperidin-1-Yl-Acetic Acid finished formulations upon request. The Piperidin-1-Yl-Acetic Acid suppliers may include Piperidin-1-Yl-Acetic Acid 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 Piperidin-1-Yl-Acetic Acid Drug Master File in Japan (Piperidin-1-Yl-Acetic Acid JDMF) empowers Piperidin-1-Yl-Acetic Acid 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 Piperidin-1-Yl-Acetic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Piperidin-1-Yl-Acetic Acid JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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