Rita Verma

Head of Global Clinical Affairs

Doctor of Medicine, more than 17 years of experience as Clinical Research Professional working in various phases (I, II and III) of Clinical Trials as well as Post Market Surveillance.

Experience in establishing Clinical Quality System and Team building.

In-depth knowledge of the methods and procedures of Clinical Trial Design, Site Start-up and Management, Clinical Monitoring, Data Management and applicable Regulatory requirements.

Expert in establishing Post Market Surveillance and Clinical Follow Up System per the European and FDA guidelines.

Rita Verma’s Session(s)

2:30 pm
Site, Sponsor, CRO Clinical Documentation Best Practices

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