Deepti Patki began working in the field of clinical research in 2009 after receiving her Masters in Clinical Research Management from the University of North Texas Health Science Center, USA. Ms. Patki has held various roles in clinical research management and has worked extensively on Phase II/III/IV industry sponsored clinical trials as well as Investigator Initiated clinical trials. She currently works in Clinical Operations at a global CRO. Deepti is passionate about teaching to help advance the clinical research workforce.

Her expertise lies in informed consent and clinical research project management. She has delivered seminars on various clinical research topics to professionals for continuing education as well as clinical research students.

Deepti has been a member of the Association of Clinical Research Professionals (ACRP) since 2010 and has also served on various committees for the ACRP.

Lawrence Reiter has almost 20 years’ experience in the Pharmaceutical Research Industry in Clinical Operations, Project Management, Quality Assurance and Compliance. His experience includes monitoring and project management across a wide variety of therapeutic areas to include drug and device studies across all phases.

Lawrence has worked in multiple regions around the world and manages global studies in over 40 countries. In addition, he is accredited by and remains in good standing with the Society for Quality Assurance as a Registered Quality Assurance Professional in Good Clinical Practice (RQAP-GCP).

Lawrence is an experienced lecturer in GCP having been directly involved in the setup and running of a non-profit training organization in South Africa that provided training across global regions to both Sponsor and site staff.