Please read and confirm that you have read and understood the following:
- Participation in clinical trials is voluntary.
- Participation in clinical trials is at no cost to participants.
- Before a volunteer can participate in a approved clinical research protocol, a informed consent document for the specific trial needs to be signed and dated by the volunteer himself to confirm that the trial was explained, that the volunteer does not have any unanswered questions, that the volunteer understands participation is voluntary and that the volunteer can withdraw from trial participation without compromizing his standard medical treatment.
- All personal information will only be used for trial purposes of an approved protocol. The approval will always be done by the Medicines Control Council and an accredited Ethics Committee.
- Personal information will only be forwarded to a third party for clinical trial purposes and only with the volunteer’s consent. The third party will always be an approved clinical trial site and site personnel. The approval will always be done by the Medicines Control Council and an accredited Ethic Committee.
- Personal information will only be stored on a database with the volunteer’s consent.
- Personal data can be updated on the secure clinical trial recruitment database, by contacting the clinical trial recruitment call center tel. number 044 874 5762 or sending an e-mail to info@clinicalresearch.co.za.
- Personal data will be deleted from the secure clinical trial recruitment center database on volunteer’s request.
- Clinical trial recruitment call center cannot take responsibility for the protection of a volunteer’s personal information referred to an approved clinical trial site. This responsibility will reside with the applicable site, which should function according to Good Clinical Practice Guidelines.
If you have any questions please contact us at info@clinicalresearch.co.za.