01 1MP Biomedicals
01 1France
01 1Blank
01 1Valid
01 1Blank
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Certificate Number : R1-CEP 2008-056 - Rev 00
Issue Date : 2013-05-17
Type : TSE
Substance Number :
Status : Valid
A Transferrin Fragment manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Transferrin Fragment, including repackagers and relabelers. The FDA regulates Transferrin Fragment manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Transferrin Fragment API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Transferrin Fragment supplier is an individual or a company that provides Transferrin Fragment active pharmaceutical ingredient (API) or Transferrin Fragment finished formulations upon request. The Transferrin Fragment suppliers may include Transferrin Fragment API manufacturers, exporters, distributors and traders.
click here to find a list of Transferrin Fragment suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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