Helpful Links

Helpful Links & Resources


Biospecimen Information

Donating Your Tissue for Research: Video
NCI Donation Brochure
Biospecimen Standard Operating Procedures and Quiz

Cancer Information

Canadian Cancer Society
Cancer Care Ontario
National Cancer Institute
National Institutes of Health

Cancer Clinical Trials Information

Cancer Clinical Trials: The Basic Workbook

Cancer Clinical Trials: The In-depth Program
PRE-ACT (Preparatory Education About Clinical Trials)
ACRP Training Program


Clinical Trials Listing
Mesothelioma Prognosis Network

Financial Aspects of Clinical Trials

CCO Draft Drug Reimbursement Policy
N2 Annual Meeting Presentation
Drug Cost Avoidance Presentation

Clinical Research Information

Canadian Institutes of Health Research
International Cancer Genome Consortium
Ontario Health Study
Cancer Research UK
Experimental Cancer Medicine Centre Network
UK Clinical Research Collaboration

Clinical Research Professionals




Drug Information Association (DIA)
Collaborative Institutional Training Initiative (CITI) Program
Ontario Telemedicine Network's Webcasting Centre
NIH Human Research Protections Training

TCPS2 - CORE (Course in Research Ethics) Tutorial

Health Canada New Investigator Clinical Trials Course

Health Canada Division 5, Part C Training

N2 Health Canada Inspection Survey

N2 Health Canada Inspection Survey Results

N2 Health Canada Delegation Log Inspection Survey Results



Initiative to Streamline Clinical Trials

Research Ethics

OCREB Online

Standard Operating Procedures

Circulating Tumor Cells
Circulating Tumor Cells
Network of Networks - Clinical Research (contact Karen Arts for login Information)
Clinical Research Impact Assessment Form
SOP Impact Assessment Procedure
SOP Start Up Procedures



ASCO: Clinical Trials Resources
Cancer Care Ontario - Symptom Management Tool
Oncology Nursing Society: Oncology Clinical Trials Nurse Competencies

Canadian Association of Nurses in Oncology: Roles in Oncology Nursing

2014 N2 - Applicability of US Regs to Canadian Research

CTEP CTC/CTCAE Mapping Document

NCI Guidelines for Investigators: Adverse Event Reporting Requirements

CTMS - Edge

Accrualnet - Strategies, Tools and Resources to Support Accural to Clinical Trials

Clinical Research Resources - Purchase Research Reference Materials

Common Terminology Criteria for Adverse Events (CTCAE)

Safety Profiler for Searching CTCAE Terms


Professional Associations


ACRP: Association of Clinical Research Professionals

SoCRA: The Society of Clinical Research Associates

ONS: Oncology Nursing Society

CANO: Canadian Association of Nurses in Oncology

Clinical Trials Regulations


Canadian Regulations

HBFB Inspectorate Division
The Personal Information Protection and Electronic Documents Act (PIPEDA)
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
Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT)


Ontario Institute for Cancer Research (OICR)


NCIC Clinical Trials Group


Radiation Therapy Oncology Group (RTOG)

Clinical Trials Support Unit(CTSU)

Network of Networks (N2)