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محتوای ارائه شده توسط Life Sciences WA. تمام محتوای پادکست شامل قسمت‌ها، گرافیک‌ها و توضیحات پادکست مستقیماً توسط Life Sciences WA یا شریک پلتفرم پادکست آن‌ها آپلود و ارائه می‌شوند. اگر فکر می‌کنید شخصی بدون اجازه شما از اثر دارای حق نسخه‌برداری شما استفاده می‌کند، می‌توانید روندی که در اینجا شرح داده شده است را دنبال کنید.https://fa.player.fm/legal
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Pathway to market: the role of Clinical Trials. Natalie Barber - Chrysalis Advisory & Peter Richmond - CAHS

31:17
 
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Manage episode 396719112 series 3427899
محتوای ارائه شده توسط Life Sciences WA. تمام محتوای پادکست شامل قسمت‌ها، گرافیک‌ها و توضیحات پادکست مستقیماً توسط Life Sciences WA یا شریک پلتفرم پادکست آن‌ها آپلود و ارائه می‌شوند. اگر فکر می‌کنید شخصی بدون اجازه شما از اثر دارای حق نسخه‌برداری شما استفاده می‌کند، می‌توانید روندی که در اینجا شرح داده شده است را دنبال کنید.https://fa.player.fm/legal

In this episode of the LSWA podcast, host Tracey Wilkinson sits down with Natalie Barber, the director of Clinical Operations at Chrysalis Advisory, and Professor Peter Richmond from the University of Western Australia.

Natalie and Peter discuss their respective roles in the clinical trial space. Peter, a paediatrician, focuses on improving children's health by conducting research on vaccines and monoclonal antibodies. He shares his involvement in every stage of the clinical trial process, from vaccine design to regulatory advisory boards.

Natalie's role is to support clinician researchers like Peter in delivering complex clinical trials. She explains the importance of understanding the protocols, engaging participating sites, and ensuring regulatory compliance.

The conversation covers the structured pathway that a drug or device must follow before being approved for the market. Natalie breaks down the phases of a clinical trial, starting from preclinical studies in the laboratory, progressing to phase 1, phase 2, and phase 3 trials involving larger populations, and even continuing with phase 4 post-marketing surveillance. She emphasises the time commitment and financial investment required, as well as the need for multicenter trials to gather data from different jurisdictions.

Throughout the episode, Natalie and Peter provide valuable insights into the world of clinical trials and the importance of evidence-based medicine. Their combined expertise offers a comprehensive understanding of the processes behind bringing new medical treatments to market.

We’d love your feedback on this podcast series, please take a moment to complete this short survey: ​​https://forms.office.com/r/W0R1cEtMjh

The LSWA podcast is brought to you by Life Sciences WA. To stay updated on LSWA and connect, visit our website https://www.lifescienceswa.com.au

This show is a proud member of the Talking HealthTech Podcast Network - the premier audio destination for cutting-edge insights and thought leadership in healthcare delivery, innovation, digital health, healthcare ICT, and commercialisation. Learn more at www.talkinghealthtech.com/podcast/network.

  continue reading

14 قسمت

Artwork
iconاشتراک گذاری
 
Manage episode 396719112 series 3427899
محتوای ارائه شده توسط Life Sciences WA. تمام محتوای پادکست شامل قسمت‌ها، گرافیک‌ها و توضیحات پادکست مستقیماً توسط Life Sciences WA یا شریک پلتفرم پادکست آن‌ها آپلود و ارائه می‌شوند. اگر فکر می‌کنید شخصی بدون اجازه شما از اثر دارای حق نسخه‌برداری شما استفاده می‌کند، می‌توانید روندی که در اینجا شرح داده شده است را دنبال کنید.https://fa.player.fm/legal

In this episode of the LSWA podcast, host Tracey Wilkinson sits down with Natalie Barber, the director of Clinical Operations at Chrysalis Advisory, and Professor Peter Richmond from the University of Western Australia.

Natalie and Peter discuss their respective roles in the clinical trial space. Peter, a paediatrician, focuses on improving children's health by conducting research on vaccines and monoclonal antibodies. He shares his involvement in every stage of the clinical trial process, from vaccine design to regulatory advisory boards.

Natalie's role is to support clinician researchers like Peter in delivering complex clinical trials. She explains the importance of understanding the protocols, engaging participating sites, and ensuring regulatory compliance.

The conversation covers the structured pathway that a drug or device must follow before being approved for the market. Natalie breaks down the phases of a clinical trial, starting from preclinical studies in the laboratory, progressing to phase 1, phase 2, and phase 3 trials involving larger populations, and even continuing with phase 4 post-marketing surveillance. She emphasises the time commitment and financial investment required, as well as the need for multicenter trials to gather data from different jurisdictions.

Throughout the episode, Natalie and Peter provide valuable insights into the world of clinical trials and the importance of evidence-based medicine. Their combined expertise offers a comprehensive understanding of the processes behind bringing new medical treatments to market.

We’d love your feedback on this podcast series, please take a moment to complete this short survey: ​​https://forms.office.com/r/W0R1cEtMjh

The LSWA podcast is brought to you by Life Sciences WA. To stay updated on LSWA and connect, visit our website https://www.lifescienceswa.com.au

This show is a proud member of the Talking HealthTech Podcast Network - the premier audio destination for cutting-edge insights and thought leadership in healthcare delivery, innovation, digital health, healthcare ICT, and commercialisation. Learn more at www.talkinghealthtech.com/podcast/network.

  continue reading

14 قسمت

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