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Pan Canadian Oncology Drug Review Provincial Advisory Group (PAG) Feedback on a code Expert Review Committee Initial Recommendation Blinatumomab (Blintz) for Acute Lymphoblastic Leukemia (Pediatric) August
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How to fill out pan-canadian oncology drug review

01
Step 1: Obtain the necessary drug submission forms from the Pan-Canadian Oncology Drug Review (pCODR) website.
02
Step 2: Complete all required sections of the drug submission forms, providing detailed information about the drug, its indications, dosing, safety profile, and clinical evidence.
03
Step 3: Submit the completed forms along with supporting documents, such as clinical trial data, to pCODR for review.
04
Step 4: Participate in the pCODR review process, which may include answering questions from the pCODR Expert Review Committee.
05
Step 5: Await the final recommendation from pCODR, which will be provided to the participating jurisdictions for funding decisions.

Who needs pan-canadian oncology drug review?

01
Patients with cancer who may benefit from access to new oncology drugs.
02
Healthcare providers, including oncologists and other specialists, who are looking for evidence-based guidance on the use of oncology drugs.
03
Payers and policy makers who make decisions about funding and reimbursement of oncology drugs in Canada.
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Pan-Canadian Oncology Drug Review (pCODR) is a process for reviewing new cancer drugs in Canada to determine their clinical and cost effectiveness.
Manufacturers of new cancer drugs seeking reimbursement in Canada are required to file pan-Canadian oncology drug review.
To fill out pCODR, manufacturers need to provide detailed information on clinical trials, patient populations, effectiveness, safety, and cost of the drug.
The purpose of pCODR is to inform decision-making on the funding of new cancer drugs in Canada by evaluating their clinical and cost effectiveness.
Information on clinical trials, patient populations, effectiveness, safety, and cost of the drug must be reported on pCODR.
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