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)