De ACRON is de branchevereniging van CRO’s in Nederland. Wij behartigen de collectieve belangen van de aangesloten bedrijven (leden). Dit doen we door middel van het organiseren van bijeenkomsten, zowel besloten als open, netwerk en lobby activiteiten met als voornaamste doel om Nederland als onderzoeksland optimaal te laten functioneren. Bekijk hieronder de agenda van evenementen van de ACRON en Contract Research Organisaties (CRO’s) in Nederland:
EUCROF Members are entitled to participate at a reduced fee: in the invite below, the EUCROF promocode can be obtained at the ACRON secretariat (firstname.lastname@example.org) When registering to the event on the EUCROF website, you just need to insert the code to pay the reduced amount.
This message is not for non-EUCROF Members, who might just wish to go to the EUCROF website and register to the Webinar section (www.eucrof.eu/webinars).
Software is used widely in clinical trials: from managing worldwide trials to finding and scheduling patients, gathering trial data, and analyzing trial results. How is the quality of the computerized systems ensured? And how do we know the data generated by these systems is reliable and robust?
Validation of software ensures that clinical data generated by these systems is done in a structured way and ensures integrity, reliability, and robustness of the generated data.
In this 1-hour webinar, you will learn why computerized systems must go through a validation process when used in clinical trials, as well as the consequences of failing to validate your systems. We will explain the requirements for validation, who is responsible and when it is necessary. Through the speaker’s experience, you will learn the why, what, and how of validation with regards to regulatory requirements.
This webinar also provides you with a walk through the process of system validation and its key deliverables. And finally, you will be shown the way to either manage the validation process of your own system or make the right considerations when selecting software for your clinical trials.
Webinar takeaways for the audience
1. Understand for which software validation is required and in which regulations requirements for validation are documented
2. Understand who is responsible for validation and what the goal of validation is
3. Know what to look for when choosing software to be used in your clinical trial
4. Understand what steps should be taken to validate your (vendors’) system
5. Be aware of the challenges in the validation process and know how to ensure a smooth process
Presenter: Marieke Meulemans