First Biennial Scientific Conference on Medicines Regulation in Africa

First Biennial Scientific Conference on Medicines Regulation in Africa

Published on Thursday, 24 October 2013 09:31 The NEPAD Agency in collaboration with the World Health Organization (WHO) and the organisational support of US-Food and Drugs Administration (USFDA) and the Drugs for Neglected Diseases initiative (DNDi) is pleased to announce the First Biennial Scientific Conference on Medicines Regulation in Africa, to take place on 2nd and 3rd December 2013, at Birchwood Hotel, Johannesburg South Africa. The theme of the conference is “Building Partnerships for Sustainable Capacity Development in Medicines Regulation in Africa”. The initiative to organise this conference is borne of the necessity for African regulatory authorities, researchers, academic institutions and industry to work together to address some of the salient issues affecting their areas of delivery of medical products and technologies to the public. The objectives of the scientific conference are to:

1. Provide a forum to share scientific advances and current best practices in regulatory science disciplines amongst policy makers, regulators, industry and scientists
2. Review current global developments in the regulatory environment and assess their impact on the commercialization of health research products as part of implementation of the Pharmaceutical Manufacturing Plan for Africa (PMPA).
3. Contribute to global knowledge on regulatory science
4. Provide inputs to the third African Medicines Regulatory Authorities Conference

Please download a copy of the draft Conference Programme here . Call for Abstracts The Organizing Committee requests submission of abstracts from interested parties, for presentation at the conference or publication in a Book of Abstracts. Regulators, researchers, academic institutions and regulatory scientists are invited to submit abstracts as below. The scientific conference topics for which the call for abstracts shall be submitted are:

1. Global regulatory environment: Where is Africa?
2. Regulatory capacity development & partnerships
3. Strengthening pharmacovigilance systems in Africa
4. Providing an enabling environment for pharmaceutical production in Africa

Interested participants should submit an abstract in one of the above four areas, of at least 250 words and not more than 300 words by 15 August 2013 by email to amrh@nepad.org  and copypaul@nepadst.org  and janet@nepadst.org . Abstracts must be submitted together with a complete abstract submission form, in Microsoft Word font Arial 11.5 Please access the abstract submission form by downloading it here and more details in the Call for Abstracts at the link here .

Conference Registration: All aspiring participants are expected to register by 25 October, 2013 by completing the registration form found here and sending the completed form in an email to nthabiseng@nepadst.org  or call +27 12 841 2833. There is a registration fee of US$50. Registration is free of charge for presenters.  

Source: African Medicines Regulatory Harmonization