Calgary Centre for Clinical Research
The Calgary Centre for Clinical Research and HiiTeC have created a new Online PSP Tutorial, which can be used for training purposes, as well as a guide when submitting your own contracts. Visit the PSP training page for more information!
March 5, 2012 - information was sent out on the clinical-trialists-L mailing list. Click here to register!
Please refer to the link below to view the Province Wide Laboratory Services and Test List for Clinical Trials and Research Studies. The Faculty of Medicine Intranet requires a Med Domain to access.
https://intranet.med.ucalgary.ca/res/Provincial%20Laboratory%20Fee%20Schedule/Forms/AllItems.aspx
February 10, 2012
CCCR has a new process for entering sub-site agreements initiated by the University of Calgary onto the Protocol Submission Program (PSP). Information can be found on our website at the following links: PSP, Sub-site Agreements, Frequently Asked Questions.
February 23, 2011
If you send invoices to Pfizer's St. Laurent, QC or Brandon, MB location, please click on the letter below regarding revised mailing addresses and A/P Enquiry Contact Numbers.
Pfizer St. Laurent QC and Brandon MB Canada Invoice Address Change
January 01, 2010
When negotiating clinical trial agreements, it is important to be aware that the institutional overhead rate has increased to 30% effective January 01, 2010. Below is a link to a letter that can be downloaded and provided to sponsors as required when negotiating overhead.
Overhead Statement Letter 2010
8 March 2011
Dr. Michael Hill recently attended the following session and wishes to pass along the information received:
Dear Stakeholder,
In follow-up to Health Canada's Good Clinical Practices (GCP) Information Sessions of this past November, we are pleased to send you our pre-inspection package, as well as some questions and answers which arose consistently during these sessions.
*Please note that the attached pre-inspection package is currently under revision and a new version will be available on our website shortly.
For further information on our program, including reports, policies, and guidance documents, please visit the GCP Program's website at the following link:
http://www.hc-sc.gc.ca/dhp-mps/compli-conform/clini-pract-prat/index-eng.php
We would like to thank you once again for attending our sessions.
Sincerely,
The Good Clinical Practices Compliance Program, Health Canada
20 January 2011
The guidelines at the link below are important reading for all researchers who prepare and sign grant applications:
11 May 2009
The Calgary Centre for Clinical Research (CCCR) will be the hub for clinical trials activity in the Faculty of Medicine. Plans are currently being drawn up to consolidate trials administration and the activity of the Heritage Medical Research Clinic on the fifth floor of the Teaching, Research and Wellness (TRW) building.
The administrative side of the CCCR will co-ordinate the approval and management of clinical health research in the faculty. This will include the 4 main components of: (1) legal services; (2) accounting services; (3) human ethics oversight and (4) impact assessment. This website will ultimately provide information and links to information necessary to conduct clinical trials and clinical health research at the University. It is my goal that we will have an entirely electronic platform for managing the clinical research process in due course.
The clinical side of the CCCR will house space and patient facilities for outpatient clinical trials. This will be the Heritage Medical Research Clinic which is managed and will continue to be managed by Carolyn Robertson, RN. The HMRC will be housed on the 5th floor of the TRW building and will have space for clinical trials co-ordinators to run trials and review patients. Please contact Carolyn for more information on the use of this space.
Michael D. Hill
Director, CCCR