QFINITY · Events · Meet QFINITY
Where you meet us in person.
An overview of the events QFINITY has taken part in or will be attending - conferences, talks and webinars. You'll often find us at ISPE and ACDM events. Stop by and talk to us in person.
Upcoming events
4th ACDM AI Symposium | June 23-24, 2025
As a long-standing active member of the ACDM and a member of the Steering Committee, Marcus Schwabedissen plays a key role in shaping the strategic direction of the symposium. With his extensive experience in optimizing clinical data management processes and implementing innovative technologies, he provides valuable input on the quality-driven, forward-looking use of AI in data-driven healthcare.
His participation highlights QFINITY’s ongoing commitment to innovation, quality, and practical advancement in clinical research.
You can find more information about the 4th ACDM AI Symposium here.
ISPE Online Workshop with QFINITY| June 17, 2025
In this one-hour online event, they will provide a practical overview of the updated 2nd Edition of the GAMP Good Practice Guide for ensuring compliance and validation of computerized systems in the GCP (Good Clinical Practice) environment. Their presentation will focus on key challenges in highly outsourced clinical landscapes, integrating emerging technologies such as AI and decentralized trials, and considerations around data integrity and data protection.
With their extensive experience in quality management and computerized systems, Frank Henrichmann and Oliver Herrmann play a vital role in bridging regulatory requirements and technical implementation. Their participation reflects QFINITY’s commitment to advancing best practices in the pharmaceutical and life sciences industries.
Learn more and register for the 2025 ISPE online workshop on the official ISPE website here.
ISPE Webinar with QFINITY | June 5, 2025
Webinar Topics:
Importance of Clinical Data: Understanding the critical role of data from clinical sites in the success of clinical trials and the risks associated with inadequate system validation or oversight.
Regulatory Expectations: An overview of EMA guidelines on computerized systems and electronic data in clinical trials, with an emphasis on compliance, data integrity, and system validation.
Challenges for Sponsors: A discussion of the difficulties sponsors face in establishing robust oversight of systems used at clinical sites, particularly in decentralized and hybrid trial models, to ensure regulatory compliance and data integrity.
This webinar is based on the “GAMP® Good Practice Guide: Validation and Compliance of Computerized GCP Systems and Data – Good eClinical Practice (2nd Edition).” It offers practical insights and best practices for system validation and effective collaboration between sponsors and clinical sites.
About the Speaker:
Frank Henrichmann brings extensive expertise in quality management and computerized systems and will share valuable insights from his work at QFINITY.
Registration:
You can register for the ISPE webinar 2025 here.