Your Journey to Becoming Inspection Ready

It is well known that building and maintaining a culture of quality is crucial to the success of a clinical trial, but how can you be sure that your methods are best practice?

The GCP Inspection Readiness forum will guide you on your journey to becoming inspection ready. Join like minded peers as you engage in high levels of interactivity and overcome your challenges in: creating a culture of quality, sponsor oversight, CAPAs, QMS and understanding the regulatory landscape. Complete your journey with our onsite mock-inspection where you will give your new skills a trial run and leave with the confidence, you are inspection ready.

As the only European forum where Clinical Quality and Operations Professionals join together in collaboration to benchmark with their peers in Big Pharma, SMEs and CROs, the GCP Inspection Readiness forum will give you the practical solutions you have been looking for.


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Your Complete Journey to Inspection Readiness

Manage Inspector Expectations by Understanding Global Regulations, with insights from bluebird bio, Johnson & Johnson and Smith & Nephew

Perfect your risk management strategy personalised to your company with case studies from Pfizer, Pierre Fabre and UCB sharing their experiences

Streamline your approach to Good Clinical Practice by ensuring your electronic systems are up to scratch, as Grünenthal and Ferring give you their top tips

Re-imagine your strategy for sponsor oversight and transform the collaborative relationship, by hearing directly from PPD and Polpharma on how they maintain transparency and take ownership of quality

Safeguard your clinical trial by understanding the principles of data integrity with expert guidance from the Good Clinical Practice Alliance and the Health Sciences Records and Archives Association

Finish Point: All –Day Mock Inspection: Put your new skills to the test and leave with the confidence you ARE inspection ready! Exploring the latest case studies from Roche and Grünenthal


See What Else is on Offer at Inspection Readiness Week

As part of the Inspection Readiness Week, we're also hosting the Trial Master Files & Inspection Readiness Forum!

Discover how you can optimise your TMF processes with presentations and insights from companies such as Pfizer, Biogen, Novo Nordisk and Syneos Health. Focusing on sponsor and CRO oversight, TMF interoperability, eTMF transition and securing senior management support – this event is the only platform where you can benchmark with the principle experts within the TMF industry through a 100% interactive program.

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GCP Checklist

With recent changes amongst GCP Guidelines, including the amendment of ICH E6 it is now more critical than ever to keep up to date and ensure a culture of readiness. View this checklist to help you on your journey to compliance and maintain a culture of quality. 



Blog: Journey to Inspection Readiness

It is well known that building and maintaining a culture of quality is crucial to the success of a clinical trial, but how can you be sure that your methods are consistent and best practice? Find out how you can curate a consistent culture of readiness in your organisation here.


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