To facilitate such interactions, while safeguarding confidentiality of data and the interests of those involved in the data collection and processing, the Network has established a Research Committee. The members are:

Southern Africa: Eric Chokunonga (Zimbabwe)
Western Africa: Abidemi Omonisi (Nigeria)
Francophone Africa: Bakarou Kamaté (Mali)
Eastern Africa: Anne Finesse (Seychelles)
Coordinator: Max Parkin (UK)

The role of the committee is to review external requests for cancer registry data with the Network members concerned, and to agree a joint response to such enquiries.

Researchers wishing to pursue research projects involving members in more than one country should submit the following, to be reviewed by committee members:

  • Research projects: submit protocol (with aims, rationale, budget and timeline). Specify proposed budgetary provisions to participating registries; proposed roles of registry investigators in data analysis and report writing and, degree of involvement in study (intellectual property rights).
  • Student research: submit protocol, dean’s letter, ethical clearance from relevant authorities.
  • Articles for publication: submit title, aims, methods, inclusion of registry investigators in data analysis, manuscript writing and publication.
  • Reports from Government Ministries (Health, Education, etc): submit a letter of support from relevant Minister or Permanent Secretary’s office, indicating title, aims, methods, inclusion of registry investigators in data analysis and report writing.

Submissions should be made via the AFCRN secretariat. The committee will discuss the application request, consult with those members potentially involved,  and give a response on terms of collaboration within 15 days of receipt of the application.


Updated on 4th December 2020