01 1PEPTIDO GmbH
01 1Liothyronine sodium
01 1Germany
Registration Number : 222MF10255
Registrant's Address : Am Kraftwerk 6, D-66450 Bexbach, Germany
Initial Date of Registration : 2010-11-05
Latest Date of Registration : 2010-11-05
A Liothyronine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liothyronine Sodium, including repackagers and relabelers. The FDA regulates Liothyronine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liothyronine Sodium 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 Liothyronine Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Liothyronine Sodium supplier is an individual or a company that provides Liothyronine Sodium active pharmaceutical ingredient (API) or Liothyronine Sodium finished formulations upon request. The Liothyronine Sodium suppliers may include Liothyronine Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Liothyronine Sodium 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 Liothyronine Sodium Drug Master File in Japan (Liothyronine Sodium JDMF) empowers Liothyronine Sodium 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 Liothyronine Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Liothyronine Sodium 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 Liothyronine Sodium suppliers with JDMF on PharmaCompass.
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