Makrocare, a global clinical services firm that provides clinical research support to pharmaceutical, biotechnology and medical devices industries, is organising a webinar on November 27 between 4 and 5.30 pm. It will impart important information about European regulation in Pharmacovigilance practice to the medical/clinical community. The webinar is to cater to the needs to continuously educate clinical research, drug safety and medical professionals in the field of Pharmacovigilance.

Key learning objectives are European union regulation for Pharmacovigilance; roles and responsibility of QPPV (European Union); practical problems and solution in Pharmacovigilance; and questions and answers.

Industry speakers and leaders like Dr Irene Fermont, vice president, Risk Management and Pharmacovigilance- ADDS; Dr Manoj Sharma, head Pharmacovigilance -Panacea; and Dr Driss BERDAI, ex-director Pharmacovigilance, EMEA and senior director - QPPV, Pfizer will share their views.

Physicians, drug safety managers, investigators, research associates, project managers and clinical professionals in clinical, healthcare, pharmaceutical, and biotech industry are expected to participate in the interaction.

Webinar can be attended on www.makrocare.com or on phone number +91 40 44346688 or email Pvwebinar@makrocare.com.