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Provision of training in good clinical practices (GCP, GCLP, CDM) for individuals involved in clinical trials and other studies involving human subjects, clinical monitors, and key institutional and regulatory stakeholders
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Organization of WHO-TDR supported training courses and workshops (e.g., Product Research and Development, Immunology and Vaccinology Applied to Dengue Infection)
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Provision of training courses associated with targeted research
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Facilitation of training and education opportunities for health research stakeholders in the region
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Ensure the implementation of GCP in clinical trials through monitoring
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Coordinate and support WHO-TDR CCTC clinical monitors and institutions that practice good research through coordination of cross-network activities
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Facilitate communication among ethics committees reviewing health research in the region
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Provision of technical assistance in the adoption and implementation of standard operating procedures (SOPs) for ethical review in the region
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Provision of technical support and services for clinical studies (such as therapeutic drug monitoring, pharmacokinetic & bioequivalence studies, high throughput screening of compounds for antimalarial activities, sensitivity tests for antimalarials & antibacterials, and analysis of antimalarial resistance genes)
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Ensure the implementation of GCP clinical trials through certification and recognition: Clinical Trial Audit Programme, GCLP Recognition Programme, Clinical Monitors Recognition Programme, SIDCER (Strategic Initiative for Developing Capacity in Ethical Review) Recognition Programme, and FERCAP Surveyor Recognition Programme
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WHO-TDR Clinical Coordination and Training Center (CCTC) , Thammasart University (Rangsit Campus)
1st Floor , Acadamic Affairs Building (formerly Executive Office of Universiade) 99 Mu 18,
Phaholyothin Road,Klongluang, Pathumthani 12121, Thailand
Telephone : (+66) 2 564 4444 (ext. 1800), Facsimile : (+66) 2 464 4398
Email : cctc.thailand@yahoo.com
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