Videos: 17th Pharmacovigilance 2018
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Virtue Insight is glad to announce 17th Pharmacovigilance 2018 to be held on 15th November 2018 in Mumbai, India. It focuses on the advancements in Pharmacovigilance, Risk Management, and Drug Safety. The field of Pharmacovigilance is growing rapidly and its development is making tremendous impacts in medical sciences and pharmaceuticals. 17th Pharmacovigilance 2018 emphasizes on how the importance and significance can be gauged by the fact that it has made huge advancements over the course of time and is continuing to influence various sectors. SPONSORS: • Principal Sponsor: Apcer Life Sciences • Gold Sponsor: Syneos Health • Exhibitors: Ab Cube, Medvigil, Elsevier KEY SPEAKERS: • A. RAMKISHAN, Deputy Drugs Controller, DDC(I) • K. BANGARURAJAN, Joint Drugs Controller (INDIA), CDSCO (HQ) • RAJENDRA SANGHAVI, Sr. Consulting Clinician & Chairman - Medical Committee, Indian Drug Manufacturers' Association (IDMA) • MAYUR PARMAR, Deputy Collector, Government Of Gujarat • DEEPA ARORA, Vice President- Pharmacovigilance & Global Head- Drug Safety & Risk Management, Lupin • ARUN BHATT, Consultant - Clinical Research & Development • SHIRAZ KANDAWALLA, Associate Director - Regulatory Affairs, Abbott • JAMAL BAIG, Country Head- Pharmacovigilance, Merck Sharp & Dohme • SANJEEV MIGLANI, Founder and Director, AWINSA Life Sciences • GURPREET SINGH, Global Head, Pharmacovigilance Operations, Novartis • SRIRUPA DAS, Associate Director - Medical Affairs, Abbott • PRADEEPA RAMAKRISHNA, Global Safety Physician/ Lead Surveillance Physician, AstraZeneca • MANOJ SWAMINATHAN, Chief Manager / Head - Global Pharmacovigilance Center, Piramal • PRAVIN GHADGE, Head of Clinical Research Services, Reliance Life Sciences • ALAP GANDHI, Head Medical Affairs, GSK • MILIND ANTANI, Leader, Pharma and Healthcare, Nishith Desai Associates • NIDHI VAISH DAS, Drug Safety, Roche Pharmaceuticals • PRASHANT BODHE, Director, CliniSearch • SUJAY KULKARNI, Senior Manager, Clinical Research and Pharmacovigilance, GSK • RANJIT BARSHIKAR, QbD / CGMP Consulting, Member Editorial Board Journal of Generic Medicines, England • PRANJAL BORDOLOI, AVP - Medical Affairs and Pharmacovigilance, Veeda Clinical Research WHO SHOULD ATTEND:- Vice Presidents, Directors, CRO’s, Heads and Managers of: Pharmacovigilance Strategy, Drug Safety/Risk Management, Information and Clinical Data Management, Clinical Research, Research & Development, Product Safety/Assurance Assessment, Patient Safety & Outcomes Research & Data Analysis, Epidemiology project management, Regulatory Affairs and Compliance, Sales & Marketing, Biotech manufacturers From the following: Pharmaceutical organizations, Generic pharmaceutical companies, Contract research organizations, Patient recruitment companies, Government- Department of health, Non-profit organizations/ Association, Consultants CONFERENCE REGISTRATION: In order to register you can simply Email: firstname.lastname@example.org or Tel: +91 44 24762472 • Early Bird Discounted Price (Ends 2nd October 2018 ) – 1 Delegate Pass – (INR 10,000 + GST (18%) per delegate) • Standard Price (3rd October 2018 Onwards) – 1 Delegates – (INR 15,000 + GST (18%) per delegate) • Conference Sponsor, Exhibition Stall (Booth) and a paid Speaker slots are also available. We also have some sponsorship opportunities available for the event, which gives you an opportunity to speak/exhibit, and create brand awareness. In addition, the networking opportunities in focused and relevant industry gathering provide the personal contact necessary for business development efforts. Get more from the event, with a broader scope bringing the whole communications value chain together. Enjoy and make the best out of our dedicated networking time, meet the leading international vendors showcasing the products of tomorrow in the co-located exhibition. Expand your knowledge of the latest business models and strategies in the high-level conference.