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The only place to meet face to face with your core labs to improve clinical quality from protocol design through regulatory submission to keep your trial on time and on budget.
Over 80% of the data that is submitted to the FDA for approval is coming from core labs. As trial complexity grows, so does FDA scrutiny. Now more than ever before poor management of lab operations could result in the loss of millions if not billions of dollars.
Join over 300 central lab outsourcing, operations and data management professionals with 200+ Pharmaceutical and Biotech Executives already signed up to attend to discuss and share strategies to build partnerships with core labs and couriers to save time and money without sacrificing quality.
Attendee #'s are the largest since 2009 with
200+ Attendees Already Signed Up to Attend!
Industry ratios are the best they've been – EVER!
With 85% Pharma and Biotech Sponsor Executives!
Why You Need to Attend:
- Improve oversight and avoid compliance related delays with new outsourcing metrics, monitoring and data reliability tools
- Get the science right the first time by ensuring your labs have the right development expertise including custom techniques in biomarker and assay development
- Avoid common logistical challenges in global trials with optimal information systems and improved reporting
- Protect patient samples with efficient sample collection, management, storage and handling strategies
- Build the right flexibility into protocol design and setup to stay on-time and on-budget
- Avoid common regulatory hurdles with simple strategies for standard safety testing
- Reduce time to submission and avoid delays in approval by ensuring you global lab partners has regional experience
- Manage costs by driving the industry towards new standards for sponsor and lab contracting
Central Labs is Designed for Your Entire Clinical Trials Team
- Clinical Operations – reduce time to submission with proven strategies to reduce common trial bottlenecks
- Outsourcing/Procurement – find the right partner to meet all of your study needs from novel biomarker assays to worldwide solutions to save time and money
- Data Management – leverage data standardization to achieve seamless transfer and integration by unlocking tools, experiences and capabilities
- Vendor Quality & Oversight - improve vendor oversight to ensure safety and compliance in global clinical trials by setting standardization criteria and defining expectations
- Researchers and Scientists – find the technical partners for immunogenicity assays, PK/PD/TK studies, flow cytometry, esoteric studies, biomarker assays, and more all in one place
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