WE BRING TOGETHER CLINICAL TRIAL EXPERTS
To discuss compliance, operational efficiency and performance optimization
Good Clinical Practice Summit
Learn how to effectively build quality risk management approaches into your clinical operations to optimize research, maintain GCP compliance, contain costs and ensure patient safety.
Global TMF Summit
With a strong focus on how to manage, process, and enhance your TMF, this year's conference program will continue to provide strategies, tools, and methods to meet your TMF needs and challenges.
Clinical Quality Oversight
The annual gathering for clinical quality, operations, management and audit professionals to engage and learn with varying clinical partners including CROs and investigator sites.
Compliance & Best Practices
Attend to hear sessions covering the top promotional advertising trends of 2020, including the FDA’s latest policies, multi-platform social media communications, the challenges of unbranded messaging campaigns, and more.
Tapas and TECH Talks
When developing a new therapy, it is more important than ever to have the future in mind from the outset. The choices you make at each step can set you up for success. Join experts from Cytiva and IQVIA for a 3-part discussion about strategies for robust and scalable processes: from research through late-stage trials.
GCP Webcast Series
How to Optimize Clinical Quality During a Global Pandemic
July 7–9, 2020 Virtual Event
This three-day event will feature perspectives from varying stakeholders as they share their experiences optimizing clinical quality during these trying times.
Fierce Biotech Presents:
Virtual Series: Clinical Trials
June 22–24, 2020 Virtual Event
Fierce Biotech’s upcoming series will cover technology’s role in clinical trials. Panel discussions include: the use of sensors, wearables and other remote monitoring devices for tracking patient statistics, real-world data and patient-centric technology, and the role manufacturing plays in clinical trials.
Virtual Clinical Trials — Online
Hear industry experts discuss the increasing pace of pharmaceutical innovation, the need to maintain data quality and integrity as new technologies are implemented and understand regulatory challenges to ensure compliance.
Virtual eRegulatory Operations Summit
This online event explores how companies can improve their electronic submission processes and protocols for RIM, and global regulatory submissions.