Clinical Development

  • Review of Clinical Development Plans
  • Assistance with designing and implementing clinical studies
  • Clinical Overviews for Common Technical Dossiers and other complex regulatory documentation
  • Input into regulatory interactions during Scientific Advice, Orphan Drug Designation and Marketing Authorisation procedures
  • Presentations to Regulatory Agencies

Pharmacovigilance

  • Causality assessments of individual adverse event reports
  • Input into key drug safety documents eg Annual Safety Reports, Periodic Safety Update Reports, Risk Management Plans, Periodic Benefit-Risk Evaluation Reports

Medical Affairs

  • Assesment of business development opportunities
  • Assitance with the development of Medical Information services
  • Training and motivation of sales force
  • Organisation and participation in Advisory Boards
  • Presentation and publication of scientific data

About IVC

Founded by Dr Veronica Tebbs in 2007 to provide client organisations with expert medical input into drug development and marketing support programmes, IVC offers in depth experience at senior levels to help you achieve your objectives.