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
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PharmaCompass offers a list of Liothyronine Sodium 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 Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Liothyronine Sodium API Price utilized in the formulation of products. Liothyronine Sodium API Price is not always fixed or binding as the Liothyronine Sodium Price is obtained through a variety of data sources. The Liothyronine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cynomel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cynomel, including repackagers and relabelers. The FDA regulates Cynomel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cynomel 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 Cynomel supplier is an individual or a company that provides Cynomel active pharmaceutical ingredient (API) or Cynomel finished formulations upon request. The Cynomel suppliers may include Cynomel 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 Cynomel Drug Master File in Japan (Cynomel JDMF) empowers Cynomel 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 Cynomel JDMF during the approval evaluation for pharmaceutical products. At the time of Cynomel 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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