13 to 15 May 2026
In person, in Melbourne, 9:00am to 4:00pm AEST
Monash Centre for Health Research and Implementation, Monash University.
Registrations now closedBuild practical evidence synthesis skills through a rigorous, hands-on program designed for clinicians, researchers and PhD students undertaking systematic reviews, scoping reviews, umbrella reviews, meta-analyses or meta-synthesis projects.
View 2026 cohortThe Fit-For-Purpose Evidence Synthesis Program provides a rigorous, practical and hands-on foundation to support participants to undertake evidence synthesis projects independently or as part of a team.
The program is suited to clinicians, researchers and PhD students preparing their first evidence synthesis or refining an existing protocol.
3-day in-person intensive with optional online support touchpoints.
3-day intensive plus optional 2 support touchpoints over 6 months.
MCHRI, Monash University, plus Zoom for optional touchpoints.
Monash MNHS-approved certificate upon completion.
In person, in Melbourne, 9:00am to 4:00pm AEST
Monash Centre for Health Research and Implementation, Monash University.
Registrations now closedDiscounts are available for students. Staff may be able to use continuing medical education funds where available.
For further information, email MCHRI.Shortcourses@monash.edu.
This program is designed for clinicians, researchers and PhD students who want to develop or strengthen practical evidence synthesis skills.
For program details or group enrolment options, please email MCHRI.Shortcourses@monash.edu.
Enrolment is subject to the relevant Monash terms, conditions, cancellation and transfer policies.
In-person training designed to build practical evidence synthesis capability.
Develop skills in protocol development, searching, screening, appraisal and synthesis.
Participants receive a Monash MNHS-approved certificate upon completion.
Fundamentals of evidence synthesis, research question development, protocol registration, search strategy and quality appraisal.
Search techniques, including Ovid MEDLINE and Ovid Embase, screening using Covidence, data extraction and risk of bias.
Meta-analysis, interpreting outcomes, publication bias and advanced synthesis types including meta-synthesis and umbrella reviews.
Participants can access optional consultations over 6 months to guide and refine their personal review project after the in-person intensive.
The program is delivered by facilitators with expertise in clinical research, biostatistics, evidence synthesis and national guideline development.
Participants learn from practitioners who apply these methods in real-world research, guideline and healthcare improvement contexts.
Guest facilitators may also be invited based on participants’ research interest