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12

Sep2017

CADTH Common Drug Review Releases New Update

On September 11, 2017, the Canadian Agency for Drugs and Technologies in Health (CADTH) released a new CDR Update (Issue 127) describing the following changes. Extended Initiation Range for January 2018 CDEC Meeting CADTH has extended the initiation range for its Common Drug Review (CDR) submissions targeting the January 17, ... Read More

14

Aug2017

CADTH Common Drug Review Releases CDR Update – Issue 126

On August 14, 2017, the Canadian Agency for Drugs and Technologies in Health (CADTH) released a new CDR Update (Issue 126) describing the following changes to the Common Drug Review (CDR) process. Extended Initiation Range for December 2017 CDEC Meeting CADTH has extended the initiation range for Common ... Read More

14

Jul2017

CADTH Common Drug Review Releases New Update

On July 13, 2017, the Canadian Agency for Drugs and Technologies in Health (CADTH) released a new CDR Update (Issue 124) describing the following changes. CDEC Meeting Added in December 2017 and Updated CDEC Meeting Dates CADTH will be holding a Canadian Drug Expert Committee (CDEC) meeting in December 2017 ... Read More

09

Jun2017

CADTH Common Drug Review Releases New Update

On June 9, 2017, the Canadian Agency for Drugs and Technologies in Health (CADTH) released a new CDR Update (Issue 122) describing the following changes. 1. Revised Advanced Notification Process for CADTH Common Drug Review Drugs Undergoing Expedited Health Canada Review Effective immediately, the mandatory advance notification requirement for drugs that are ... Read More

28

Mar2017

CADTH’s Updated Guidelines for the Economic Evaluation of Health Technologies – 4th Edition Now Available

The updated guidelines recognize the substantial advances that have been made in the methods of economic evaluation and they offer up-to-date guidance on the best practices for determining the economic value of health technologies. Available for download at the following link.

17

Mar2017

New CADTH Processes and March Newsletter

New CADTH Processes Expanding CADTH’s Drug Review Processes to Include Radiopharmaceuticals In collaboration with the participating jurisdictions, CADTH is pleased to announce that they will accept submissions for Radiopharmaceutical Submissions and Other Process Alignment Implementations effective April 1, 2017. Applicants/Submitters planning to file a submission or resubmission for a radiopharmaceutical on ... Read More

15

Mar2017

CADTH Special Event: New Guidelines for the Economic Evaluation of Health Technologies: Canada

CADTH is hosting an online or in person event on Tuesday, March 28, 2017 to release the fourth edition of the Guidelines for the Economic Evaluation of Health Technologies: Canada. The Guidelines are intended to help produce credible and standardized economic information that is relevant and useful to decision-makers in Canada’s ... Read More

13

Sep2016

Feedback on Proposed Revisions to Patient Input Template for CDR and pCODR

CADTH is inviting stakeholder comments on proposed changes to the patient input template for the CADTH Common Drug Review (CDR) and the pan-Canadian Oncology Drug Review (pCODR). Patient input is used by CADTH review teams and by the expert committees of the CDR and pCODR programs: the CADTH Canadian ... Read More

26

Aug2016

Registration is Underway for the CAHR Market Access 201 Course

The Canadian Association for Healthcare Reimbursement (CAHR) is hosting Market Access 201-Fundamentals of Reimbursement in Canada. This one-day training course is a continuation of Market Access 101 and offers a deeper dive into Market Access strategies. The program will be emceed by Dr. Jeffery Hoch from the Department of ... Read More

26

May2016

CADTH CDR and pCODR Engagement with the pCPA

Effective immediately, CADTH will be formally engaging with the pan-Canadian Pharmaceutical Alliance (pCPA) and will be including the pCPA office in the CADTH Common Drug Review (CDR) and pan-Canadian Oncology Drug Review (pCODR) processes. This will provide an opportunity for the pCPA office to receive relevant information on drugs reviewed ... Read More