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Trial consent now much easier
Posted 18 February 2026 PM
National Health and Medical Research Council (NHMRC) has endorsed a new consent form for trial participants designed to be clear and participant-centred.
Developed by CT:IQ (Clinical Trials: Impact & Quality), of which MA is an executive committee member, the new InFORMed Participant Information and Consent Form (PICF) template is flexible to allow researchers to think critically about which components need to be included, and which are not relevant to the trial being conducted.
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Posted 18 February 2026 PM
National Health and Medical Research Council (NHMRC) has endorsed a new consent form for trial participants designed to be clear and participant-centred.
Developed by CT:IQ (Clinical Trials: Impact & Quality), of which MA is an executive committee member, the new InFORMed Participant Information and Consent Form (PICF) template is flexible to allow researchers to think critically about which components need to be included, and which are not relevant to the trial being conducted.
To see the whole article, please login
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