Aspen API. More than just an API.
01 1Aspen Oss B. V.
02 1Farmhispania S. A.
03 1Sicor de Me(´)xico,S. A. de C. V.
01 1Rocuronium Bromide
02 1Rocuronium bromide
03 1Rocuronium bromide "Teva"
01 1Mexico
02 1Netherlands
03 1Spain
Aspen API. More than just an API.
Registration Number : 227MF10199
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2015-08-06
Latest Date of Registration : 2020-10-01
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Registration Number : 227MF10139
Registrant's Address : Balmes 85, Atico, 08008 (Barcelona), Spain
Initial Date of Registration : 2015-05-14
Latest Date of Registration : 2020-06-19
Registration Number : 227MF10201
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2015-08-06
Latest Date of Registration : 2016-09-02
A Rocuronium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rocuronium, including repackagers and relabelers. The FDA regulates Rocuronium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rocuronium 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 Rocuronium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rocuronium supplier is an individual or a company that provides Rocuronium active pharmaceutical ingredient (API) or Rocuronium finished formulations upon request. The Rocuronium suppliers may include Rocuronium API manufacturers, exporters, distributors and traders.
click here to find a list of Rocuronium 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 Rocuronium Drug Master File in Japan (Rocuronium JDMF) empowers Rocuronium 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 Rocuronium JDMF during the approval evaluation for pharmaceutical products. At the time of Rocuronium 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 Rocuronium suppliers with JDMF on PharmaCompass.
We have 3 companies offering Rocuronium
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