Impetus to literature surveillance in pharmacovigilance

on wheels of automation

Regular screening and analysis of global scientific literature is indispensable pharmacovigilance (PV) process for reporting suspected adverse reactions of medicinal products. With this objective in mind, the focus of current webinar is:

1. Literature monitoring - To fulfill expedited and non-expedited reporting requirements

2. Limitaions - Conventional literature surveillance methods employed routinely

3. Pluses - System-enabled global literature screening .
                  In absolute compliance to Appendix 2 of GVP module VI

4. Sophisticated tool - Organized means to perform literature screening

5. Literature automation - Technology support in Good Pharmacovigilance Practices (GPP) compliance

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