GCP Directions Conference
Virtual Education and Networking for Clinical Research Professionals Navigating GCP and Inspection Readiness - July 27-30, 2026
GCP Directions is a free, multi-day virtual conference designed to bring the clinical research community together for practical, candid conversations about compliance, oversight, and inspection readiness.
Across four focused days, we explore what is changing in the regulatory landscape, what it means operationally, and how to translate evolving expectations into stronger, more sustainable trial oversight.
No hype. No theory-only sessions. Just real-world insight and meaningful engagement.
Why GCP Directions?
GCP Directions goes beyond a traditional webinar format.
Each day combines:
- Focused educational sessions
- A sponsor-led panel sharing real-world experience
- Live Q&A sessions designed for candid, practical dialogue
- Interactive discusssions that allow participants to compare approaches
This format bridges interpretation and execution. Attendees hear what guidance says, how trial sponsors are applying it, and where challenges still exist.
GCP Directions creates space for practical insight, peer comparison, and thoughtful discussion about inspection readiness, oversight, and the future of compliance.
Four Days. Four Critical Focus Areas. July 27-30, 2026.
Each year, GCP Directions follows a consistent thematic structure so attendees can engage in the areas most relevant to their role.
Day 1: Quality Oversight
Understand how to establish and demonstrate control through risk-proportionate oversight, using signals across systems, vendors, and processes to identify where attention is needed.
Day 2: Risk Management
Translate oversight into action by identifying, assessing, and managing risk—embedding risk-based approaches across the clinical trial lifecycle.
Day 3: Trial Master File
Strengthen your TMF to reflect the true story of the trial, ensuring completeness, quality, and timeliness as evidence of oversight and decision-making.
Day 4: Future-Ready Clinical Operations
Explore how emerging technologies, data strategies, and new ways of working are reshaping clinical trials while maintaining regulatory control.
Inaugural 2025 Event Highlights
GCP Directions launched with strong participation from across the clinical research community. The inaugural event drew over 500 registrants representing sponsors, sites, and service organizations, with the majority bringing significant industry experience.
2025 session highlights:
- Interpreting ICH E6(R3) and operationalizing new expectations
- Strengthening TMF health and documentation clarity
- Oversight and relationship management with CROs
- Inspection trends across FDA, EMA, and global authorities
- Generative AI and the future of compliance infrastructure
Each year builds on the foundation of open dialogue and sponsor-driven learning. We are currently building the agenda for 2026 and plan to release it soon. Click below to view the detailed agenda from 2025.
Who Should Attend
GCP Directions is designed for clinical research professionals working across:
- Clinical Operations
- Quality and Compliance
- TMF and Document Management
- Clinical Systems
- Vendor Oversight
- Inspection Readiness
- Risk Management
Whether you lead strategy or execute day-to-day oversight, this conference is built to provide relevant, practical insight.
Registration
Reserve your spot for this year’s GCP Directions
Registration is free.
Interactive sessions are designed to preserve meaningful discussion and may have participation limits.
Click below to secure your access and receive updates as the full agenda is announced.
GCP Directions is hosted by Just in Time GCP, a leading clinical compliance consultancy focused on inspection readiness, TMF oversight, and operational alignment. Click here to view our most requested services and don’t hesitate to contact us directly if we can be of any assistance.
