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Overview

The 5th in the series of Global Animal Health Conferences is organised with the support of the Organising Committee partners and funded by the Bill & Melinda Gates Foundation (BMGF).

The conference is scheduled to take place on 17 November 2016, at the Lalit hotel, in New Delhi, India.

Government representatives, regulators, senior animal health experts, industry, academia, inter-governmental bodies and international organisations will exchange views on the importance of good regulatory governance of veterinary medicines. Sound governance and alignment to international standards promotes improved animal health that in turn contributes to socio-economic development. The focus will be on India and South Asia and the need for appropriate regulatory systems to enable the registration, market access and market control of quality assured animal health products, and the contribution this makes to the ‘One Health’ vision.

Adjacent Event: Pre-Conference Workshop on "Good Regulatory Practice for the Marketing Authorisation of Veterinary Products in an Asian Context",
14-16 November 2016, for Regulatory Authorities only.

A printed copy of the presentations will be provided to workshop attendees.

The presentations of the conference will not be printed. Both the workshop and the conference presentations will be available online to attendees.

If you are interested in attending the Pre-Conference Workshop or the Global Animal Health Conference 2016, please complete your application online:

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We only have a limited number of places available. Please note that your registration is not valid until you received a confirmation email by DIA.  

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Organising Committee

 
 

Learning objectives

Conference Aims
To increase political and stakeholder awareness and support for better animal health and better access to quality assured animal health products.To increase the understanding of the needs of different stakeholders and regulators in the region with regard to regulatory harmonisation.

Conference Objectives

  • Identify challenges relating to the registration process and improved market access for authorised veterinary medicines and how to promote the implementation of suitable systems.
  • Explore the importance and benefits of regulatory convergence, including alignment to international standards and guidelines, and identify the key parameters enabling countries to implement them.
  • Identify the needs, responsibilities and challenges relating to control of product quality during manufacture and control of products throughout the distribution chain.
  • Through case studies, explore the needs for capacity building, mutual recognition and regional organisations in the efficient implementation of regulatory systems.
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