Speaker: Geoffrey Schick
As the business climate in health care continues to transform, entities engaged in clinical research are evaluating the costs and benefits of participating in clinical research. Is it just about the bottom line in the financial statements? Join PFS Clinical and Bio-Optronics for a webinar to learn about ideas and tips to ensure the mission of the research department/institute is aligned with the parent organization, and opportunities to communicate the value that may not show up in your “P&L Statement.”
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February 28th - 11:00 AM
Improving patient throughput and access to care is a critical priority for VA. Addressing these core VA patient needs not only elevates the quality of care patients receive, it also improves their overall satisfaction with the surgery experience.
Join us for a free webinar where you will learn how to combine optimized pre-op scheduling and real-time status tracking to maximize the efficiency and safety of VA surgical services from check-in through discharge.
You’ll learn methods and best practices for:
March 20 and 22, 2018 - 10:00 a.m. PT | 1:00 p.m. ET
These digital “eTools” can help you improve research efficiency and quality. But they also require additional regulatory compliance activities at the research site and knowledge of FDA computer system validation requirements. Remember, the sponsor or software vendor can help, but they cannot completely address these obligations for you.
In this complimentary webinar, you will learn the key regulatory requirements a research site must be aware of before implementing eTools, including helpful tips on how to build a risk-based compliance plan. In addition, you will hear how a leading eCTMS software vendor, Bio-Optronics, is helping sites take advantage of eTools and remain compliant with FDA Part 11 requirements.