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SANCTR Working Group
Purpose of SANCTR Working Group
To ensure that the South African National Clinical Trial Registry complies with international standards for clinical trial registration and that the Registry meets the needs of its users (researchers, health professionals, funders and sponsors, policy makers and the lay public).

Dr Tamara Kredo
Project Supervisor (staff)
Ms Elizabeth Pienaar
Project manager (staff)
Dr Duduzile Ndwandwe
Project Coordinator (staff)
Mr Keith Ross
MRC IT Division
South African Medical Research Council
Dr Lesibana Malinga
National Department of Health, South Africa
Steering Committee
Purpose of Steering Committee
To provide strategic advice and support to the Working Group with regards to the South African National African Clinical Trials Registry (sanctr.samrc.ac.za).
Members
Ms Thulile Zondi
National Department of Health, South Africa

Dr Tshilidzi Muthivhi
National Department of Health, South Africa
Dr Tamara Kredo
Project Supervisor
Clinical Trial Registry project (PACTR and SANCTR)
Senior Specialist Scientist, Cochrane South Africa, South African Medical Research Council


Dr Lesibana Malinga
National Department of Health, South Africa

Mr Patric Charls
MRC IT Division
South African Medical Research Council
Mr Keith Ross
MRC IT Division
South African Medical Research Council


Ms Thesandree Padayachee
Programme Manager
Health Systems Research Unit
Health Systems Trust (HST)


Dr Theresa Burgess
Senior Lecturer & Committee Member
National Health Research Ethics Committee (NHREC)
Dr Duduzile Ndwandwe
Project Coordinator
Clinical Trial Registry project (PACTR and SANCTR)
Senior Scientist, Cochrane South Africa, South African Medical Research Council


Ms Elizabeth Pienaar
Project manager
Pan African Clinical Trials Registry
Cochrane South Africa, South African Medical Research Council
Dr Dorah Diale
Deputy-Director
Clinical Trials Unit
South African Health Products Regulatory Authority,South Africa
Funders
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