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01 1Evonik Operations GmbH
02 1Cambrex Profarmaco Milano S. r. l.
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01 1Lormetazepam
02 1Lormetazepam Lormetazepam
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01 1Germany
02 1U.S.A
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
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PharmaCompass offers a list of Lormetazepam 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 Lormetazepam manufacturer or Lormetazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lormetazepam manufacturer or Lormetazepam supplier.
PharmaCompass also assists you with knowing the Lormetazepam API Price utilized in the formulation of products. Lormetazepam API Price is not always fixed or binding as the Lormetazepam Price is obtained through a variety of data sources. The Lormetazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Loramet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loramet, including repackagers and relabelers. The FDA regulates Loramet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loramet 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 Loramet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loramet supplier is an individual or a company that provides Loramet active pharmaceutical ingredient (API) or Loramet finished formulations upon request. The Loramet suppliers may include Loramet API manufacturers, exporters, distributors and traders.
click here to find a list of Loramet 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 Loramet Drug Master File in Japan (Loramet JDMF) empowers Loramet 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 Loramet JDMF during the approval evaluation for pharmaceutical products. At the time of Loramet 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 Loramet suppliers with JDMF on PharmaCompass.
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