ACRP 2026
Conference Focus
Clinical operations, study/site management, 21 CFR Part 11/Annex 11 compliance
Overview
ACRP 2026, organized by the Association of Clinical Research Professionals, is a premier annual gathering dedicated to the clinical research workforce. It serves as a vital hub for professionals focused on clinical operations, study management, and site-level execution. The conference is uniquely positioned to bridge the gap between regulatory requirements and practical, on-the-ground implementation, offering deep dives into 21 CFR Part 11 and Annex 11 compliance. Beyond regulatory updates, the event emphasizes the professional development of clinical research coordinators, monitors, and project managers. By fostering collaboration across the clinical trial ecosystem, ACRP 2026 provides actionable insights into improving trial quality, efficiency, and patient safety, making it an essential event for those driving the operational success of pharma and biotech development programs.
Why Attend
Attendees gain critical insights into evolving regulatory landscapes and best practices for site management. It offers unparalleled networking with peers and industry leaders, facilitating knowledge exchange on operational challenges. Professionals will walk away with actionable strategies to enhance trial compliance, streamline study workflows, and advance their careers within the clinical research enterprise.
Key Topics & Sessions
- •Clinical Trial Site Management
- •21 CFR Part 11 & Annex 11 Compliance
- •Risk-Based Monitoring Strategies
- •Clinical Research Workforce Development
- •Patient Recruitment and Retention
- •Data Integrity and Quality Management
- •Decentralized Clinical Trials (DCTs)
- •Regulatory Inspection Readiness
- •Clinical Trial Technology Integration
- •Ethics and Human Subject Protection
Who Should Attend
Conference History
The Association of Clinical Research Professionals (ACRP) was founded in 1976 to provide a voice for clinical research professionals. Over nearly five decades, its annual conference has grown into the leading educational and networking event for the clinical research workforce, consistently evolving to address the industry's most pressing operational and regulatory challenges.
Venue & Location
Hyatt Regency Orlando, located in the heart of Orlando, Florida, offering extensive meeting facilities for large-scale industry gatherings.
Related Conference Categories
This conference covers topics in the following pharma and life sciences domains. Explore more events in each category using our conference directory filters.
Resources & Links
About the ACRP 2026 Conference
ACRP 2026 is a in-person event scheduled for 2026-04-24 to 2026-04-27 in Hyatt Regency Orlando, FL. The conference focuses on clinical operations, study/site management, 21 cfr part 11/annex 11 compliance. This event is categorized under Clinical Operations, Regulatory & Compliance in our conference directory.
ACRP 2026, organized by the Association of Clinical Research Professionals, is a premier annual gathering dedicated to the clinical research workforce. It serves as a vital hub for professionals focused on clinical operations, study management, and site-level execution. The conference is uniquely positioned to bridge the gap between regulatory requirements and practical, on-the-ground implementation, offering deep dives into 21 CFR Part 11 and Annex 11 compliance. Beyond regulatory updates, the event emphasizes the professional development of clinical research coordinators, monitors, and project managers. By fostering collaboration across the clinical trial ecosystem, ACRP 2026 provides actionable insights into improving trial quality, efficiency, and patient safety, making it an essential event for those driving the operational success of pharma and biotech development programs.
Professionals attending conferences like ACRP 2026 gain access to cutting-edge insights, peer networking, and exposure to the latest technologies shaping the pharmaceutical and biotechnology sectors. Whether you are evaluating new vendors, seeking regulatory updates, or expanding your professional network, industry conferences remain one of the most effective ways to stay current in life sciences.
Regulatory conferences are essential for staying current with evolving requirements from the FDA, EMA, and other global regulatory bodies. Understanding compliance frameworks such as 21 CFR Part 11 and ICH guidelines is critical for pharmaceutical software development and validation.
Looking for guidance on which conferences to attend or how to build your event strategy for 2026? Book a meeting with the IntuitionLabs team to discuss your priorities and how we can support your team.