I am a Senior Executive with more than 25 years of experience in various managerial roles in Quality, Regulatory Affairs CMC, and R&D in major pharmaceutical companies. 

 

I have gathered extensive expertise in these disciplines and can build a bridge between GMP/Quality Assurance and Regulatory Affairs CMC  during the whole lifecycle of a drug product. This ensures smart regulatory strategies, compliant dossiers and smooth registration processes, supported by high quality data, lean processes and sound science.

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More information can be found on my       Profile.