Pharmacovigilance Summit 2016

Building and enhancing pharmacovigilance and risk management capacity and capability

Pharmacovigilance Summit 2016

India is the fourth largest producer of pharmaceuticals in the world and is also emerging as a hub for clinical trials. With more clinical trials and clinical research activity being conducted in India, there is an immense need to understand and implement pharmacovigilance.

With increased scrutiny faced by companies, drug recalls and adverse reactions getting significant attention by traditional and digital media the challenges faced by the company are forcing it to take a more proactive approach to PV.

In this conference, we shall discuss approaches to scale up existing rudimentary PV system and cultivate spontaneous reporting systems in the function.

Speakers

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In this conference we shall discuss approaches to scale up existing rudimentary PV system and cultivate spontaneous reporting systems in the function.

Key Topics of Discussion Day 1

  • Better PV data management
  • Overcoming challenges in effective PV analytics
  • Preparing for PhV Audits and Inspections
  • Developing an effective risk management plan
  • Proactive risk minimization operational practices
  • Effective implementation of Automated signal management processes

Who will you meet?

VPs, GMs & Functional Heads of:

  • Pharmacovigilance
  • Drug Safety
  • Regulatory Affairs
  • Clinical Affairs
  • Medical Affairs
  • Clinical Research
  • Quality control & assurance
  • Patient safety
  • Sales, Marketing & Business Development

Who should attend?

  • International and regional health authorities and regulators
  • Pharmaceutical & Biotechnology companies
  • Clinical Research Organization (CRO) service providers
  • Business Process Outsourcing (BPO) service providers
  • Risk Management Software developers
  • Pharmacovigilance Audit Firms
  • Pharmacovigilance consultancy service providers

Gold Partner

Advertising Partner

Business Development Partner

Media Partners

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