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Course Marketing Authorisation, Pricing and Distribution in Africa
Marketing Authorisation, Pricing and
Distribution in Africa:
Truth vs Hype
2019-03-22 2019-03-22 NH Frankfurt Airport West Kelsterbacher Str. 19-21 65479 Frankfurt-Raunheim nhfrankfurtairportwest@nh-hotels.com +49 6142 990-0 +49 6142 990-100

Marketing Authorisation, Pricing and Distribution in Africa: Truth vs Hype

Ghana, Nigeria, Cameroon, the Republic of Congo, Ethiopia, Kenya, Tanzania, South Africa, Namibia, Botswana and Zimbabwe

Marketing authorisation and distribution of pharmaceuticals in the Sub-Saharan African (SSA) markets, that is, Ghana, Nigeria, Cameroon, the Republic of Congo, Ethiopia, Kenya, Tanzania, South Africa, Namibia, Botswana and Zimbabwe. Get practical hints directly from an industry expert!
Topics
  • Local scientific offices, agents and distributors: What is required?
  • Communication with local authorities
  • CPP requirements
  • Reimbursement options for generics and originator drugs
  • Kenya, Tanzania, South Africa, Namibia etc. at a glance

Aims and objectives

Are you responsible for one or more of the SSA markets, that is, Ghana, Nigeria, Cameroon, the Republic of Congo, Ethiopia, Kenya, Tanzania, South Africa, Namibia, Botswana and Zimbabwe? Then you should not miss this course, which addresses regulatory affairs, pricing, market access and distribution in these markets.
After having attended this course, you will have a thorough understanding of how to professionalise your communication with local authorities, of the potential distribution paths and of how to work successfully in these markets.
Who should attend
This course addresses the needs of healthcare professionals in the pharmaceutical industry who share responsibility for markets on the African continent.
Those involved in regulatory affairs, pricing, market access and distribution in particular will benefit from this course.
Your speaker
Gagan Datta
Pharma Bavaria International GmbH


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Abbreviations, Glossary

List of abbreviations

Many abbreviations for processes, documents and authorities, amongst others, are used in all regulatory areas. We have compiled the most important ones for you.

Our list of abbreviations can be freely downloaded here.

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Pharma Webcast Global RA & PV

Pharma FORUM Webcast International

We would like to invite you to join our live webcasts, where local regulatory affairs and vigilance experts will inform you every two months of the latest news and trends in global marketing authorisation and drug safety.

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More on our quality criteria

Quality guaranteed!

IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards.

An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2017 - 09.2018 produced a result of 1.6 (based on a school grading system of 1-6).

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