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Medcast news and blog

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GPs are pivotal to early recognition of genetic conditions — PRECISE and Medcast delivers a hub for rapid upskilling

Genomics is now part of everyday general practice. The PRECISE Genomics in Primary Care hub gives Australian GPs fast, practical tools to recognise genetic red flags, guide testing and support timely referrals.

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Non-invasive prenatal testing/screening (NIPT/S) - clinical fact sheet and MCQ
Non-invasive prenatal testing/screening (NIPT/S) - clinical fact sheet and MCQ
PRECISE Education Team

An increasing number of pregnant patients are seeking advice from their GP about prenatal genetic testing. This FastTrack covers non-invasive prenatal testing/screening, including how it works, indications, limitations, and different types of testing panels. 30mins each of RP and EA CPD available.

READ ON | 10 Min Read
Reproductive genetic carrier screening - clinical fact sheet and MCQ
Reproductive genetic carrier screening - clinical fact sheet and MCQ
PRECISE Education Team

Reproductive genetic carrier screening (RGCS) may be considered for patients during their preconception counselling stage. This FastTrack covers who should be offered RGCS, which conditions it screens for, and what to do with the results. 30mins each of RP and EA CPD available.

READ ON | 10 Min Read
PRECISE Genomics Research Project: Increasing Capacity for Precision Medicine in Primary Healthcare
PRECISE Genomics Research Project: Increasing Capacity for Precision Medicine in Primary Healthcare
Kate Clutton

The PRECISE (Practitioner Readiness, Education and Capabilities, with Implementation Science Evaluation) Genomics Research Project, brings together expertise in genomics, education, and implementation science for a truly collaborative effort to revolutionise precision medicine in primary healthcare.

READ ON | 5 Min Read