2nd GCP Inspection Readiness, Leverage Tools, Training, and Technology to Achieve a Confident State of GCP Inspection Readiness, December 4-6, 2023, Hybrid Event, Philadelphia
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Achieve confidence that your company is GCP inspection ready by walking through every step of the inspection preparation and execution process. Leave having heard directly rom the regulators themselves about inspection trends, what you need to implement to ensure you are prepared, and understand how technology and effective training can be utilized to drive a culture of quality, and a continued state of GCP inspection readiness.

Kristen Hunter
VP, Content
MOMENTUM EVENTS

In-Person Experience

FULL ACCESS

As an in-person attendee, you’ll have full access to all of the presentations, panels, roundtables, and networking opportunities on the main agenda.

Virtual Experience

PARTIAL ACCESS

You’ll get the most value from this event by attending in-person, but if you absolutely cannot, a few of the main conferences sessions will be live-streamed for those choosing the virtual experience. Please note the roundtables are for the in-person experience ONLY.

Select your Experience

FDA REPRESENTATIVES AND LEADERS FROM THESE COMPANIES HAVE ATTENDED THE SUMMIT IN THE PAST

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Top Reasons to Attend

Understand the impact of ICH E6(R3) on GCP inspections and how to prepare 

Assess Critical to Quality factors to establish the building blocks for your GCP inspection readiness plan  

Ensure you are executing a proportionate risk-based approach to inspection preparation and readiness

Leverage available tools such as audits, mock inspections, training, even your TMF, to assess and mitigate risk and ensure inspection readiness 

Outline the sequence of events for an actual inspection to ensure a comprehensive understanding of the stakeholders who should be involved and roles required 

Discuss quality culture as the heart of any successful inspection readiness plan 

DISCOVER WHAT OUR LAST YEAR’S ATTENDEES ARE SAYING ABOUT THE EVENT!

Loved!  It was so nice to hear about inspections from the inspectors’ view, including good practices to implement based on inspection feedback.   – Director, Quality, IDEAYA BIOSCIENCES

This was my first in-person event with Momentum Events, it won’t be my last.   – Manager, QA & Compiance, STIRIS RESEARCH

Great conference for both new and seasoned colleagues to learn baseline inspection activities from prep to hosting!  – Principal, FDC CONSULTING SERVICES

I enjoy attending this conference as people are willing to share their experiences candidly and honestly.  – Executive Director, Quality and Compliance, ORGANON
The opportunity to network with other CQA peers and other stakeholders from big and small pharma, has been incredible.  Loved the frank discussions.   – Associate Director, Clinical Quality Operations, MERCK 
Great conference.  Some brought the kindling, some brought the spark, and together we created an inspired fire!  – Senior Director, Quality Assurance Auditing, INSEPTION GROUP 

Our 2023 Sponsors

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media partner

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SPONSORSHIP OPPORTUNITIES are available

Sponsorship is a great way to enhance your brand’s visibility and help you connect with top-level decision-makers, innovators, and industry disruptors. There are a number of ways to maximize branding opportunities at the summit.

Become a 2023 Sponsor

WHO SHOULD ATTEND

This event is developed for professionals from pharmaceutical, biotechnology and medical device companies, CROs, clinical service and technology providers as well as those professionals from sites who have responsibilities in any the following areas:

  • Inspection/ Inspection Readiness
  • Compliance/ Clinical Compliance/ Regulatory Compliance
  • Auditing
  • Quality Management/ Clinical Quality Management
    ○ Clinical Quality Assurance/ QA/ CQA
    ○ Clinical Quality Control/ QC/ CQC
  • Quality Operations/ Quality Systems/ Quality Processes
  • Regulatory Affairs
  • Clinical Operations/ Management/ Research/ Development
  • Clinical Outsourcing/ Vendor Oversight and Management/ Strategic Partnerships/ Third-Party Management and Oversight
  • Clinical Risk/ Quality Risk/ Risk Assessment/ Risk Management
  • Site Monitoring/ Site Management/ Study Management/ Trial Management
  • Good Clinical Practice/ GCP
  • Clinical Data