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 – 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