Earlier this year, Cytovance Biologics, Inc., a manufacturer of mammalian and microbial biologics, assigned Edwin Miranda as the Vice President of Quality. He is expected to lead Cytovance’s quality functions. Who is Edwin Miranda and what are the other things he has done for Biologics?

Cytovance Biologics, Inc., welcomed Edwin Miranda in their ranks as the Vice President of Quality. Miranda got over 33 years of experience in quality assurance as well as biologics and cosmetics. He is also a member of the faculty of University of Michigan School of Kinesiology and has 19 papers about Biologics. He also has experience in encompassing solid and liquid oral does, as well as in the cosmetics industry. Dr. Jesse McCool, the Senior Vice President of Cytovance’s Research and Development says that the company is very fortunate to have an experienced executive join their team.

Edwin Miranda has an experience in quality control before. He was the leader of the Quality Assurance team for the launch of the New Drug Application or NDA or Keppra. He also served as the Vice President of Quality Assurance in URL Mutual Pharmaceuticals, Inc., Piramal Critical Care, Inc., and Legacy Pharmaceutical Packaging.

Because of his success in the world of pharmaceutical quality assurance, Edwin Miranda has been a known name in his industry. Developing a remediation plan to correct 483 observations, he received the Establishment Inspection Report (EIR) in good standing. Among his research papers are “Endogenous Secretory RAGE Increases with Improvements in Body Composition and its Associated with Markers of Adipocyte Health”, and a study about high fat meals and their effect on human’s RAGE (receptor for advanced glycation end-products) with no effect before aerobic exercise.

Cytovance Biologics is known for its stints in manufacturing and producing therapeutic proteins and antibodies for microbial fermentation and mammalian cell culture. They offer Biologics services with their state-of-the-art facilities located at Oklahoma City.

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