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PharmaCompass offers a list of Ticlopidine 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 Ticlopidine manufacturer or Ticlopidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ticlopidine manufacturer or Ticlopidine supplier.
PharmaCompass also assists you with knowing the Ticlopidine API Price utilized in the formulation of products. Ticlopidine API Price is not always fixed or binding as the Ticlopidine Price is obtained through a variety of data sources. The Ticlopidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ticlopidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ticlopidine, including repackagers and relabelers. The FDA regulates Ticlopidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ticlopidine 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 Ticlopidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ticlopidine supplier is an individual or a company that provides Ticlopidine active pharmaceutical ingredient (API) or Ticlopidine finished formulations upon request. The Ticlopidine suppliers may include Ticlopidine API manufacturers, exporters, distributors and traders.
click here to find a list of Ticlopidine 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 Ticlopidine Drug Master File in Japan (Ticlopidine JDMF) empowers Ticlopidine 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 Ticlopidine JDMF during the approval evaluation for pharmaceutical products. At the time of Ticlopidine 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 Ticlopidine suppliers with JDMF on PharmaCompass.
We have 6 companies offering Ticlopidine
Get in contact with the supplier of your choice: