#None #Toronto #Xtalks Webinar #IVD Clinical Trials #Clinical Performance Studies

Webinar on Global IVD Clinical Performance Studies

In the ever-evolving field of precision medicine, in vitro diagnostic (IVD) devices play a critical role. They are especially important for ensuring appropriate subject eligibility for targeted treatments in managing malignancies and chronic diseases. A fascinating upcoming webinar hosted by Xtalks aims to illuminate the intricacies of global IVD clinical performance study monitoring. This free webinar, titled "IVD Study Steps for Success: Safety and Quality of Global IVD Clinical Performance Studies," will delve into the common findings highlighted by global regulatory bodies, emphasizing the significance of compliance and safety in IVD clinical performance and clinical trials.

Significance of the Webinar

The webinar offers valuable insights on how organizations can navigate the ever-changing landscape of regulatory, ethical, and quality standards in IVD clinical studies. Participants will learn about various expectations set by international regulators and the operationalization of quality and safety protocols in IVD studies. In addition, expert speakers will share effective strategies and practices that can bolster global IVD clinical performance studies.

Key Topics to be Addressed

• - Common regulatory insights and findings raised by international authorities in IVD clinical performance studies
• - Steps necessary to establish and maintain quality and safety standards in these studies
• - The importance of robust quality management systems that comply with a multitude of regulations, including the International Council for Harmonisation – Good Clinical Practice (ICH GCP), Good Clinical Laboratory Practice (GCLP), and more

The hosts, Dr. Caoifa Dougan and Dr. Charlene Robb of Almac Diagnostic Services, will lead an engaging discussion, further explaining how IVD studies can be conducted effectively while ensuring data integrity and regulatory compliance.

Who Should Attend?

This event is designed for professionals across various sectors, including pharmaceuticals, biotechnology, and healthcare, or anyone involved in the development or management of IVD clinical studies. If you are keen on enhancing your understanding of compliance and regulatory standards in the context of IVD device development, this is an opportunity you won't want to miss.

Practical Insights and Registration

Webinar attendees will gain access to practical insights that can be immediately implemented within their organizations. The session will also cover the necessary steps for aligning global IVD clinical performance studies with the varying standards of different countries, thus safeguarding the interests of pharmaceutical or diagnostic sponsors.

To participate in this insightful discussion, register for the free webinar, scheduled for Thursday, November 13, 2025, at 11 AM EST (5 PM CET), by visiting the Xtalks website.

About Xtalks

Xtalks is dedicated to providing quality education through webinars and digital content for the life sciences, healthcare, and medical device sectors. Each year, Xtalks serves thousands of industry professionals looking to stay current with the latest developments and regulations in their respective fields. It facilitates networking and knowledge sharing among professionals by featuring industry experts and thought leaders on critical subjects.

Don't miss this chance to enhance your understanding and practice of IVD clinical performance studies—register today!