Webinar Date & Time
21 July 2026 from 11:00 AM to 12:30 PM (CEST)
Webinar Overview
This presentation provides an overview of audit readiness principles tailored for Clinical Research Associates (CRAs) and their managers (administrative and operational). It focuses on equipping CRAs with the knowledge and practical tools needed to prepare for and successfully navigate audits and inspections.
Key areas include understanding regulatory expectations, maintaining high-quality and inspection-ready documentation, ensuring compliance with ICH GCP principles, and effectively supporting sites before, during, and after audits. The session also highlights common audit findings and best practices to mitigate risks and ensure consistent quality across clinical trial activities.
For CRA managers, the session additionally emphasises their role in oversight, team readiness, and fostering a quality culture.
The ultimate objective is to strengthen CRA confidence and capability in maintaining continuous audit readiness and contributing to a culture of compliance and quality.
Presenter
Maria Veleva
Founder and Principal Consultant
Velev Consulting Ltd.
Maria Veleva, MD, is the Founder of Velev Consulting Ltd., a clinical quality consultancy that supports life sciences companies with tailored solutions to enhance trial quality and operational effectiveness.
Maria began her career as a Clinical Research Associate (CRA), gaining hands-on experience in clinical trial execution and site engagement. She brings nearly 25 years of experience in global clinical research, including 10 years specialising in quality.
She partners with organisations across the life sciences sector to optimise processes and procedures, reduce risks, and drive efficiency in clinical trials. Her work ensures that studies are conducted to the highest quality standards, supporting regulatory approval while safeguarding patient safety. Maria’s expertise has established her as a trusted advisor in the industry.
Maria is also a sought-after trainer and speaker, having presented at numerous international conferences. She holds leadership roles in professional organisations such as RQA, EF GCP, and others.
Attendance Fee
€ 90,- for non-EUCROF members
€ 60,- for EUCROF members
Deadline for registration
20 July 2026 at 6 p.m. CEST
How to register?
1) Go on the REGISTRATION PAGE and click on the orange button “GET TICKETS”
2) Check your order and click on the green “CHECKOUT” button
3) Fill in all the necessary information and validate your order
Confirmation
You will receive 2 confirmation emails:
A) One from Eventbrite with your invoice
B) One from “Eucrof” with all the necessary information to connect the D-Day!
Questions?
Should you have any questions about registration, invoices or connection, do not hesitate and contact us by email at webinar@eucrof.eu
By registering to the webinar, you give your authorisation to the webinar organizers to use your email address and personal information to communicate with you about this event and future initiatives. To stop receiving their communications, please contact the organizers directly at info@eucrof.eu.
