Until further notice, all Scientific Advice meetings will be held virtually using video-conferencing technology. All efforts will be made to maintain the security and confidentiality of the meetings. Recording will not be permitted by any party.
Read about the CADTH Scientific Advice process
The CADTH Scientific Advice Program does not offer Scientific Advice once a phase III trial (or pivotal trial) has been initiated. CADTH provides early Scientific Advice on prospective drug development plans at a stage where the feedback provided can still be incorporated into development plans. CADTH does not offer advice on the analysis of existing data.
Yes, as long as these questions are posed in the Briefing Book for CADTH Scientific Advice and all eligibility requirements are met.
Read more about the type of advice offered through the CADTH Scientific Advice Program
Applicants should consider the amount of information that can be discussed in a Scientific Advice meeting when determining the final number of questions to submit. As a general rule, ten (10) questions is usually the maximum that can be discussed at the meeting; however, this is dependent on the complexity of the questions. More or fewer questions may also be reasonable. CADTH may provide feedback on the number of questions slated for the meeting if there are concerns.
If minutes from regulatory Scientific Advice are provided (this is optional), CADTH will consider the regulatory Scientific Advice already provided in developing the CADTH Scientific Advice. This may assist in avoiding conflicting Scientific Advice in some cases or in the suggestion of ways to address the needs of HTA, while still addressing regulatory needs, if possible.
|CADTH Scientific Advice Meeting||Pre-Submission Meeting|
|Purpose||To assist in drug development planning by providing feedback on evidence requirements from an HTA and payer perspective||To facilitate efficient submission preparation and filing; sponsors can introduce drugs and clarify procedural and/or application requirements|
|Timing||Very early in the drug development process (a number of years before Health Canada approval and before pivotal trials have been initiated)||Late in the drug development process (within 12 months of filing the application for CADTH drug reimbursement review)|
|Scope||Includes communication with the sponsor, consultation with experts, and preparation by CADTH; results in the creation of a CADTH product (CADTH Record of Scientific Advice)||Meeting with sponsor; no CADTH product|
No. Health Canada or INESSS may not participate as observers in the parallel Scientific Advice process with CADTH and NICE. Applicants may wish to consider applying for parallel Scientific Advice with Health Canada and CADTH, with INESSS participating in an observatory role.
According to the Confidentiality Guidelines for Scientific Advice, all documents submitted by applicants and produced by CADTH as part of the Scientific Advice Program are to be kept confidential between the applicant and CADTH (including authorized recipients and patient representatives, as applicable) except as agreed by expressed, advance, or written permission from both CADTH and the applicant, or as required by law or by order of a legally qualified court or tribunal. For parallel Scientific Advice, the applicant agrees to the disclosure and exchange of information related to the project with the participating organizations.
No. Members of CADTH expert committees will not have access to the CADTH Record of Scientific Advice, nor will they be aware that the drug under review previously received CADTH Scientific Advice.
Experts are chosen based on their relevant clinical, economic, and HTA expertise. The assessment of conflicts of interest is also part of the process.
Read more about the involvement of experts in the CADTH Scientific Advice Program.
The CADTH Scientific Advice Program includes clinical, economic, and HTA experts as part of the process. A representative from publicly funded drug plans is not included as one of the experts for a Scientific Advice application.
Current members of CADTH expert committees will not be involved as experts for CADTH Scientific Advice. However, past members could be engaged as experts, if appropriate.
Read more about the involvement of experts in the CADTH Scientific Advice Program.
No. The applicant will not have input into selecting the experts who assist in developing CADTH Scientific Advice. The applicant may suggest the type of clinical specialty or designations a clinical expert engaged by CADTH should ideally have. We will be interested in feedback from applicants on the quality of discussion and input provided by the experts we select. We will use this input to help us select appropriate and effective experts for future CADTH Scientific Advice applications.
Patient engagement in clinical trial design is being discussed in various forums internationally. If applicants have sought input from patients in their product development plans related to the design of pivotal clinical trials, CADTH requires this information so it can be taken into account when preparing the CADTH Scientific Advice. All information related to consultations with patients on clinical trial design should be included; however, the country where the consultations were carried out should also be indicated. If applicants have not sought this type of input from patients, it should simply be indicated in section 4.5 of the Briefing Book (Summary of Patient Engagement, if available).
No. Patient representatives do not attend the CADTH Scientific Advice meeting according to the standard CADTH Scientific Advice process at this time. For parallel Scientific Advice with CADTH and NICE, patient representatives may be invited to attend and participate in the Scientific Advice meeting.
No. Patient involvement is part of the CADTH Scientific Advice process for all applications. However, applicants have the opportunity to determine what, if any, information submitted by them or produced by CADTH as part of the CADTH Scientific Advice Program is shared with patient representatives. Applicants indicate permission to share information as part of the online application form for the CADTH Scientific Advice Program. Applicants also have the option of completing a Patient Drug Information Form, which will be shared with patient representatives in order to provide background information on the drug to enable a relevant conversation with CADTH staff.
Read more about patient involvement in the CADTH Scientific Advice Program.
According to the CADTH Scientific Advice disclaimer, the Scientific Advice provided to the applicant may not be taken into account in any future CADTH assessments or recommendations. The Scientific Advice provided is not permitted to be included as part of a submission to the CADTH drug reimbursement review. These processes have been put in place in order to maintain the integrity of the drug formulary review process and minimize any perceived biases that may result from the disclosure of any advice received.
An application is reviewed for eligibility and availability of preferred meeting dates prior to the approval and confirmation of the application. Once the application is approved and the time period for the Scientific Advice meeting has been mutually agreed to, the first invoice will be issued. The applicant may withdraw the application prior to the confirmation of the application, without penalty.
Changes in meeting dates, after confirmation by both parties, are challenging for CADTH. CADTH requires as much advance notice as possible in order to manage date changes. CADTH will make every attempt to accommodate date changes if required for good reason; however, accommodation cannot be guaranteed. In the case of a meeting date change, CADTH will retain the fees already paid but will shift the remaining payment schedule to align with the new meeting date.
If an applicant withdraws from the CADTH Scientific Advice Program, CADTH will not refund fees already paid. Depending on the point of withdrawal, an additional partial charge may apply based on costs incurred to date and work completed. The applicant will be provided with an invoice for any additional fees within 30 days of withdrawal from the Program.