Resources
HICT Program Documents
HICT Funded Project Descriptions
Cancer Information
Cancer Research Information
Canadian Institutes of Health Research
International Cancer Genomics Consortium
Experimental Cancer Medicine Centre Network
National Cancer Research Network UK
Clinical Trials Listing
Clinical Research Professionals
Education
Clinical Trials Networks Best Practices
Drug Information Association (DIA)
Collaborative Institutional Training Initiative (CITI) Program
NIH Online Tutorial: Human Participant Protections Education for Research Teams
Ontario Telemedicine Network’s Webcasting Centre
Research Ethics
Clinical Trials Regulations
Canadian Regulations
Health Canada Health Products and Food Branch (HPFB) Food and Drug
Regulations for Clinical Trials
The Personal Information Protection and Electronic Documents Act (PIPEDA)
Ontario Health Information Protection Act (PHIPA)
CIHR: PIPEDA: Questions and Answers for Health Researcher
Guidance for Records Related to
Clinical Trials
Health Canada Inspections Report
Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans
International Regulations
ICH Good Clinical Practice (GCP) Guidelines
USA Food and Drug Administration (FDA) Code of Federal Regulations, Title
21
Office for Human Research Protection (OHRP), US Department of Health and
Human Services
Protocol Development
NCI Cancer Therapy Evaluation Program Protocol Templates and
Guidelines