E-Book

This eBook shares tips and best practices to guide researchers through the investigator-initiated trial process while staying compliant.

Insights into the site selection process and the information sites provide as part of site feasibility questionnaire completion.

Examine the current state of industry resources, resourcing implications, and the way we can now think of work: remote, hybrid, or on-site.

Learn how to prepare for an upcoming FDA inspection, what to expect during the inspection, and steps to take following inspection close.

Learn how your organization can implement the Whole Product Approach and how Advarra uses this method to help research sites.

Download this eBook to learn about the individuals who dedicate their talents to give patients an opportunity for healthier and longer lives.

This report outlines key survey findings, and offers suggestions as we work towards an industry-wide solution

This report is based on surveys and interviews with organizational leaders from top U.S. biotech and pharmaceutical companies.

As clinical trials grow more complex, this eBook reviews how a CTMS may help your organization address challenges as you conduct research.

This eBook outlines how clinical research sites and sponsors can effectively work together to improve their relationship.

Download our report to learn more how the COVID-19 pandemic impacted the future of the clinical research workforce.

This eBook investigates shifting fiscal priorities and strategizes how sites can ensure effective financial management post-pandemic.