Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Operations GmbH
02 1Cambrex Profarmaco Milano S. r. l.
01 1Lormetazepam
02 1Lormetazepam Lormetazepam
01 1Germany
02 1U.S.A
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 222MF10179
Registrant's Address : Rellinghauser Strasse 1-11 45128 Essen, Germany
Initial Date of Registration : 2010-06-23
Latest Date of Registration : 2017-03-13
Registration Number : 228MF10036
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2016-02-02
Latest Date of Registration : 2021-12-02
A Lormetazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lormetazepam, including repackagers and relabelers. The FDA regulates Lormetazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lormetazepam 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 Lormetazepam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lormetazepam supplier is an individual or a company that provides Lormetazepam active pharmaceutical ingredient (API) or Lormetazepam finished formulations upon request. The Lormetazepam suppliers may include Lormetazepam API manufacturers, exporters, distributors and traders.
click here to find a list of Lormetazepam 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 Lormetazepam Drug Master File in Japan (Lormetazepam JDMF) empowers Lormetazepam 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 Lormetazepam JDMF during the approval evaluation for pharmaceutical products. At the time of Lormetazepam 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 Lormetazepam suppliers with JDMF on PharmaCompass.
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