Clinical Research Coordinator Society (CRCS) Forums
About CRCS Forums
The CRCS is a community comprising clinical research coordinators across
various public healthcare institutions in Singapore. CRCS seeks to address
the training and educational needs for clinical research coordinators involved
in supporting the conduct of research studies.
As part of these educational efforts, CRCS forums are held several times
a year, as a platform for information sharing, exchange of ideas and networking
across the community. CRCS also collaborates with the Clinical Research
Professional (CRP) community in Singapore in organizing these educational
initiatives.
CRCS Forums
Presentation materials (with speakers’ agreement) from past CRCS forums are available for download below:
CRCS Forum (26 Jan 2024)
-
Looking Back at 2023
By Sumitra Sachidanandan, Regulatory Consultant
Innovation Office & Clinical Trials Branch
Health Products Regulation Group
Health Sciences Authority Singapore -
Updates from NHG: Get Ready for ECOS & Updates to Minimum Training Requirements for DSRB submissions
Ms Zhang Cailian, Specialist
Office of Human Research Protection Programme, NHG Group Research & Innovation
Past CRCS Forums
CRCS Forum (6 Jan 2023)
-
Looking Back at 2022
Sumitra Sachidanandan, Regulatory Consultant
Innovation Office & Clinical Trials Branch
Health Products Regulation Group
Health Sciences Authority Singapore
CRCS-CRP Forum (2 Jan 2022)
-
Looking Back at 2021
Ms. Sumitra Sachidanandan, Regulatory Consultant - GCP Unit
Innovation Office & Clinical Trials Branch
Medical Products Pre-market Cluster
Health Products Regulation Group
Health Sciences Authority Singapore
SCRI-NHG CRCS Forum & CRC Appreciation Day 2021
-
Managing the impact of clinical trials during the COVID-19 pandemic
Ms. Sumitra Sachidanandan, Regulatory Consultant
Innovation Office & Clinical Trials Branch
Health Products Regulation Group
Health Sciences Authority Singapore -
Learn more about the event here.
CRCS-CRP Forum (3 Dec 2019)
-
Looking back at 2019
Ms. Sumitra Sachidanandan, Regulatory Consultant – GCP Unit
Innovation Office & Clinical Trials Branch,
Medicinal Products Pre-market Cluster,
Health Products Regulation Group,
Health Sciences Authority -
Requirement of Appropriate Consent for Conduct of Human Biomedical Research and Handling of Human Tissue
Dr. May Thu MA
Senior Manager, Biomedical Research Regulation Branch, Regulatory Compliance & Enforcement Division, Health Regulation Group, Ministry of Health
CRCS-CRP Forum (07 Dec 2018)
-
Looking back at 2018
Ms Sumitra Sachidanandan
Regulatory Consultants - GCP Unit, Innovation Office & Clinical Trials Branch, Medicinal Products Pre-market Cluster, Health Products Regulation Group, HSA
-
Post Activation of Human Biomedical Research Act: Compliance and Risks
Dr Yeo Jing Ping
Director, Office of Research Integrity, Compliance and Ethics, SingHealth
-
Monitoring Programme for Human Biomedical Research Studies
Ms Jaslin Tan Shen Fong
Senior Executive, Research Quality Management Unit, Research & Development Office, National Healthcare Group (NHG)
CRCS-CRP Forum (14 Sep 2018)
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CRCs/CRPs and CIS: Developing Sound Communication and Interpersonal Skills (CIS) Is Essential for Success
Dr Aamir Shaikh, MD, DPBM
Founder, Health Care Consultant, Assansa
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Conflict Management / Problem Solving
Mr Nelson Wong
Founder & Director, CSI Medical Research
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Why Service Excellence Matters and How to EXC3ITE (Execute) It?
Mr Chan Peng, Tech Observer Asia Pacific