Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 219MF10052
Registrant's Address : 21, chemin de la Sauvegarde F-69130 Ecully
Initial Date of Registration : 2007-02-13
Latest Date of Registration : 2007-02-13
A Salicylic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicylic Acid, including repackagers and relabelers. The FDA regulates Salicylic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicylic 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.
click here to find a list of Salicylic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicylic Acid supplier is an individual or a company that provides Salicylic Acid active pharmaceutical ingredient (API) or Salicylic Acid finished formulations upon request. The Salicylic Acid suppliers may include Salicylic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Salicylic Acid 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 Salicylic Acid Drug Master File in Japan (Salicylic Acid JDMF) empowers Salicylic 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 Salicylic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Salicylic Acid 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 Salicylic Acid suppliers with JDMF on PharmaCompass.
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