Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1PCAS S.A.
02 1Olon S. p. A.
01 1Glycopyrronium Bromide
02 1Glycopyrronium bromide
01 1France
02 1Italy
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Glycopyrronium bromide "For manufacturing purposes only"
Registration Number : 230MF10066
Registrant's Address : 21,chemin de la Sauvegarde 21 Ecully Parc - CS 33167 69134 Ecully Cedex France
Initial Date of Registration : 2018-05-21
Latest Date of Registration : 2025-08-21
Registration Number : 304MF10139
Registrant's Address : Strada Rivoltana Km 6/7 20053 Rodano Milano Italy
Initial Date of Registration : 2022-10-05
Latest Date of Registration : 2022-10-05
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PharmaCompass offers a list of Glycopyrronium Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Glycopyrronium Bromide manufacturer or Glycopyrronium Bromide supplier for your needs.
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A Copyrrolate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Copyrrolate, including repackagers and relabelers. The FDA regulates Copyrrolate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Copyrrolate 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 Copyrrolate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Copyrrolate supplier is an individual or a company that provides Copyrrolate active pharmaceutical ingredient (API) or Copyrrolate finished formulations upon request. The Copyrrolate suppliers may include Copyrrolate API manufacturers, exporters, distributors and traders.
click here to find a list of Copyrrolate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Copyrrolate Drug Master File in Japan (Copyrrolate JDMF) empowers Copyrrolate 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 Copyrrolate JDMF during the approval evaluation for pharmaceutical products. At the time of Copyrrolate 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 Copyrrolate suppliers with JDMF on PharmaCompass.
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