Templates for Informed Consent and Participant Information Sheet

by Donna Russell

Collecting biospecimens for research from your community is a long-term commitment. It requires earning and keeping their trust by being as transparent as possible. It requires following the highest ethical, regulatory and legal standards.And it should include a mechanism for providing feedback to the community on the research that has been done using their samples. In some cases, there may be risks to ethnic and social groups or communities due to the release of aggregate research findings even when no individually identifiable information has been revealed. In addition, some populations or groups have specific beliefs about the disposition and use of their specimens, which should be respected. We provide the following templates:

  • informed consent to collect biospecimens during pregnancy
  • participant information sheet

8th January 2013 • comment

Templates from an investigator-led trial in Cameroon: the CAMPS trial (also available in French)

by Lawrence Mbuagbaw

During the setting up of our trial in Cameroon we met several operational issues that we needed to overcome. For some of these issues we developed some tools and we have made them available here so that other research groups can use them in their clinical trials.

13th May 2011 • comment