Discover the keys to more successful, less risky early drug development with fresh insights into keeping your studies on track and clear of the common mistakes that can add time, expense, and headaches to your projects.

The understanding of the oligomerization and aggregation potential of peptide candidates is key for the development of long acting and stable drugs. In this on-demand webinar, you will learn more about:

• The fundamental of aggregation behaviors
• Techniques to monitor and measure peptide aggregates
• How to get an operating window to mitigate risk of aggregation

Watch now for answers to these questions and more:

• What is an external comparator and where can we see these specifications?
• What is the FDA draft guidance on real world evidence (RWE)?
• What are the indications for external comparators?
• What are the best practices for fit-for-purpose real world data (RWD) and RWE?

Watch your free, on-demand webinar from Pharma Ignite, presented in partnership with IQVIA, for insights into innovative approaches to creating RWE and using it to communicate the value of your products.

Watch now to explore:

• Trends in retrospective healthcare research innovation
• Innovative approaches and solutions to complicated health economics research questions
• Recent case studies illustrating how IQVIA helped customers generate the required RWE

Access on-demand insights in this hour-long webinar from Pharma Ignite, presented in partnership with IQVIA.

Watch now for answers to these questions and more:

• What is an external comparator and where can we see these specifications?
• What is the FDA draft guidance on real world evidence (RWE)?
• What are the indications for external comparators?
• What are the best practices for fit-for-purpose real world data (RWD) and RWE?

View the webinar on-demand to discover:

• How to overcome common data quality challenges
• How you can apply data quality concepts in your organization
• How data quality measures can help provide transparency for better research
• IQVIA’s systematic approach to monitoring data quality
• Use cases for RWD application and utilization

Discover the keys to more successful, less risky early drug development with fresh insights into keeping your studies on track and clear of the common mistakes that can add time, expense, and headaches to your projects.

Find out how your electronic data capture (EDC) systems and processes can keep pace with the demands of today's increasingly complex clinical trial landscape.

• What are the best practices for database design?
• How can I deliver quality along with speed while managing database build activities?
• How can I combine tools, processes, and teams to enable accelerated study-start up and reduce cycle times?

Learn how you can efficiently and effectively set up EDC (electronic data capture) databases for your clinical trials, while promoting the highest standards of data quality. Watch at your convenience as EDC database experts from eClinical Solutions share their insights into ensuring accurate, complete, and compliant data are produced for your important clinical trials.

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