Integrating Clinical Strategy and Project Management for Cost-Effective Clinical Investigations

FREE ON-DEMAND WEBINAR
August 20, 2024

Integrating Clinical Strategy and Project Management for Cost-Effective Clinical Investigations

The focus of this webinar is to help medical device professionals run cost-effective and successful clinical investigations.

Although cost-effective and successful may not always be compatible, focusing on important aspects early in the preparation phase of a clinical investigation is crucial.

These aspects include: clinical strategy, clinical study design, clinical project management, and data management. Prioritizing and getting these right early on, can reduce the likelihood of issues occurring during a clinical study.

Using a case study approach, Bianca Lutters, Head of Clinical Operations, and Caesar Roseboom, Clinical Project Manager at Qserve, will join forces with Chris Rush, Solutions Engineer at Greenlight Guru.

Together, they will discuss how those aspects can help medical device companies run a compliant clinical investigation that results in high-quality data and fewer delays.

Watch for free

Specifically, this webinar will cover:

Why starting early with the clinical strategy and clinical investigation design is beneficial
The importance of site and country selection for both timelines and data quality in your study
How a proper set-up of your database and data management are key for the collection of high-quality data

Who should attend?

Clinical Affairs Professionals and Management
Clinical Operations Professionals and Management
Clinical Researchers and Project Managers
Regulatory Professionals and Management
Medical Device Executives

Hosted by

Moderator:
ETIENNE NICHOLS

Medical Device Guru,
Greenlight Guru

Speaker:
BIANCA LUTTERS

Head of Clinical Operations,
Qserve

Speaker:
CHRIS RUSH

Solutions Engineer,
Greenlight Guru

Speaker:
CAESAR ROSEBOOM

Clinical Project Manager,
Qserve

About Greenlight Guru

Greenlight Guru is the leading connected, cloud-based platform purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle.

Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster and with less risk.

Visit our homepage to learn more.

About Qserve

Our mission is to help improve patient safety and health by supporting the advancement of biomedical technology. We assist medical device and in-vitro diagnostics manufacturers worldwide with market access, medical device approvals, clinical trials and achieving and maintaining regulatory compliance.

We are passionately working for our customers on regulatory, quality and clinical challenges and see it as our responsibility to create a diverse global team of professionals who share the same passion for medical device technology, a high standard of quality, competence and customer service, and enjoy the fun of working on this together every day.

Visit their website to learn more.

Featured Capabilities:

Featured Capabilities:

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