01 1HAS Healthcare Advanced Synthesis SA
02 1Patheon Austria GmbH & Co KG
01 2Pyridostigmine bromide
01 1Switzerland
02 1U.S.A
Registration Number : 221MF10103
Registrant's Address : Via Industria, 24 6710 Biasca Switzerland
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2009-05-27
Registration Number : 227MF10212
Registrant's Address : St. -Peter-Strasse 25, 4020 Linz / Austria
Initial Date of Registration : 2015-08-18
Latest Date of Registration : 2015-08-18
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PharmaCompass offers a list of Pyridostigmine 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 Pyridostigmine manufacturer or Pyridostigmine supplier for your needs.
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A Bromuro de piridostigmina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromuro de piridostigmina, including repackagers and relabelers. The FDA regulates Bromuro de piridostigmina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromuro de piridostigmina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Bromuro de piridostigmina supplier is an individual or a company that provides Bromuro de piridostigmina active pharmaceutical ingredient (API) or Bromuro de piridostigmina finished formulations upon request. The Bromuro de piridostigmina suppliers may include Bromuro de piridostigmina 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 Bromuro de piridostigmina Drug Master File in Japan (Bromuro de piridostigmina JDMF) empowers Bromuro de piridostigmina 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 Bromuro de piridostigmina JDMF during the approval evaluation for pharmaceutical products. At the time of Bromuro de piridostigmina 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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