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
  • Causality assessments
  • Annual Safety Reports
  • Periodic Safety Update Reports
  • Risk Management Plans
  • Periodic Benefit-Risk Evaluation Reports
Medical Affairs
  • Assessment of business development opportunities
  • Assitance with the development of Medical Information services
  • Organisation and participation in Advisory Boards
  • Presentation and publication of scientific data
  • Training and motivation of sales force
  • Training of clinical development personnel
  • Assistance with the production and review of training materials
High Quality

In Pharmaceutical Medicine whether preparing material for a regulatory dossier, presenting to a Licensing Authority or generating training material, high quality is not an optional extra - it should be the only option available.


Pharmaceutical Medicine is very demanding and challenging, timelines and priorities can change at short notice. Island View Consulting understands this and will always endeavour to respond flexibly to evolving circumstances.


Accuracy is paramount when dealing with clinical data and working in medical science. The data and facts must be correct, the reasoning must be clear and credible, and all should be presented in an unambiguous and accessible way. There is no other way.


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