

This year we heard our esteemed speaking faculty share experiences on how to build and initiate effective clinical quality risk management strategies for emerging companies through Expert Panels, Workshops, and Networking Sessions.
Thank you to our conference Chair and Speaking Faculty
Thank you to our 2022 Sponsor and Consortium Partner
2023 Sponsorship Opportunities Are Open
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.
For more details on sponsorship and exhibition opportunities, please contact Michael Williams at michael@momentumevents.com
Top Reasons to Attend

Assess clinical risk using available resources to guide the development of your clinical risk management plan

Utilize mock inspections as a quality tool to focus risk mitigation efforts

Understand the current regulatory environment and the critical elements of changing regulations that impact clinical quality risk management

Implement quality measurement tools such as tolerance limits and key indicators to maintain compliance

Discuss best practices for vendor oversight and how to ensure your partners focus on quality

Identify best practices for building quality into your culture and processes from the start

Achieve a constant state of inspection readiness with already available tools and resources

Engage with your peers on real life examples of issue identification and management
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:
- Quality Management/ Clinical Quality Management
- Clinical Quality Assurance/ QA/ CQA
- Clinical Quality Control/ QC/ CQC
- Quality Operations/ Quality Systems/ Quality Processes
- Clinical Operations/ Management/ Research/ Development
- Compliance/ Clinical Compliance/ Regulatory Compliance
- Auditing
- Inspection/ Inspection Readiness
- 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
- Regulatory Affairs