Programme |
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Learn all the latest policies, critical issues, industry developments and strategies to enable you to maintain the highest ethical standards in healthcare research through our 6 unique tracks.
Please click here to download the Session Listings.
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Tracks |
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(1) |
Institutional Review Board / Ethics Review Board |
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This track is designed to provide a common platform for IRB / research ethics professionals to share their concerns, problems, strategies, and useful innovations pertaining to ethical review of human subject research. The sessions in this track will cover imperative issues from IRB framework and review tools, IRB education, accreditation, and self-assessment.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track. |
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(2) |
Quality Management & Quality Improvement in Research |
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This track will provide an opportunity to learn and discuss how Quality Management and Quality Improvement programs can improve compliance and efficiency among Investigators, IRBs, Sponsors, CROs and other research administration offices. Sessions in this track will also provide insights on the quality of computerised systems, audits and inspections in clinical trials.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track.
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(3) |
Regulatory & Legal Issues in Research |
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This track will provide an opportunity to learn and discuss the concepts and fundamentals of regulations pertaining to human subjects’ research, with representatives from various regulatory agencies in Asia Pacific. At the same time, the track provides an opportunity to enhance knowledge on the various legislations and legal requirement pertaining to human subject research in the Asia Pacific.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track.
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(4) |
Industry & Clinical Research Professionals |
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This track covers issues related to the planning and conduct of research, especially of complex clinical trials. The sessions will cover topics on challenges in conducting trials in Asia Pacific, effective project management & monitoring skills, pharmacovigilence/ drug safety and risk management, application of Good Clinical Practice (GCP), Responsible Conduct of Research, Research Integrity, training and education for clinical research professionals.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track.
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(5) |
Population Requiring Additional Protections |
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This track aims to provide an understanding of the concept and definition of vulnerable populations. The track will also introduce the delegates to non-conventional vulnerable populations. It will also discuss the key conceptual and ethical problems that may arise in research with vulnerable populations, and how extra protection can be implemented to protect population requiring additional protection.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track.
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(6) |
Hot Topics in Research Ethics |
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This track will cover in greater depth on a wide range of pressing issues in research ethics. The sessions are designed to cover a spectrum of crucial topics such as informed consent, special concerns in social and behavior research, research involving complementary medicine, tissue banking for research, phase I research and other issues that are avidly debated at all stratum of research ethics platform.
Please click here to download the session listing for this track.
Stay tuned for full information on sessions in this track.
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For more enquiries on programme, please email
enquiries@aprec-nhg.com.sg
