Resources

THE VALUE OF DRUG SAFETY MONITORING


  • Track regulatory activity and emerging safety

  • Simplify monitoring of adverse drug reaction case reports

  • Identify evidence that is not currently available in competitor’s drug information ā€“ to help you claim a safety advantage

  • Identify drug safety signals with timely and accurate information


THE PROCESS OF MONITORING IS BASED ON 4 KEY STEPS


  • Step 1 – Data collecting (subscription)

  • Step 2 – Data processing (digitizing)

  • Step 3 – Search organization (implementation of the search system into the database according to key words (medicine name, INN, etc.)

  • Step 4 – Creation of final reports with indications of AR mentions in articles, if found


AS A RESULT, you can login into your individual account and check the reports with links to PDF articles

Process of monitoring includes:


  • Specialized medical and pharmaceutical printed media

  • Online media

  • Social networks (micro-blogs)

  • Forums

  • Videos

  • Presentations


VITAL BENEFITS INCLUDE:


  • Accuracy

  • Time saved

  • Transparency

  • PDF clipping

  • A Business track record since 2007

  • Following the standards of the Guideline on Good Pharmacovigilance Practices

  • Customizable weekly/monthly reports

  • Information on competitor’s promotional activities

  • Mentions of the company in media for sentiment


HOW TO GET STARTED


SEND THE INQUIRY & we will start the process according to your requirements (period, monitoring array, report frequency, etc.)


The search process takes into account the experience of large companies within the sphere of pharmacovigilance which is based on effective procedures developed according to European Union Directives or Food and Drug Administration (FDA) Regulations


YOU will then receive detailed reports with key references to the sources used