Webcast series:
All about Data Integrity

Senior SME Computerized System Validation & Data Integrity EU Bob Verhoeff is a Subject matter expert for Computerized System Validation in the pharmaceutical industry and is working at the Life Science consultancy department of ProPharma Group, with 23 years of experience in the area of Commissioning, Qualification and Validation (CQV). Bob has served as IT compliance specialist, Validation engineer and Data Integrity expert in regulated environments at Medical Device and Pharmaceutical companies in international context. As a Data Integrity advisor and trainer, Bob has provided insights in DI quality improvement plans for multiple life science projects both in the Netherlands and throughout Europe. His strengths include leadership, advisory, organization change management, business process analyses, and program/project management engagement. As a practitioner and technologist, Bob has performed validation resiliency projects and Data Integrity assessments to define the IT readiness for drug product and medical device launches.
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Senior Consultant Data Integrity and CSV John has been actively involved in the pharmaceutical industry for the past 30 years with international experience in the UK, Europe and the USA. His experience covers laboratory analysis, process validation and Pharmaceutical Quality Assurance with a specific focus on Risk Based Computer System Validation. Skilled in U.S. Food and Drug Administration (FDA), Validation, Quality Assurance, Quality System, and Verification and Validation (V&V), John has experience on a wide range of pharmaceutical projects ranging from corporate SAP implementations and upgrades, COTS applications, analytical and manufacturing systems and Data Center Infrastructure qualification. He has additional experience in Supplier Audits, internal audits and in site preparation for regulatory inspections.