04.04.25 -- Scaling Gene Therapy Clinical Trials Through The Lens Of Ophthalmology

Gain insight from several clinical operations experts into the significance of meticulous contract examination when choosing an outsourcing partner.

Learn more about the best practices for EHR-to-EDC integration and the immense potential of the type of transfer as clinical trials move toward greater efficiency.

Informed consent is essential in clinical research. However, when participants lose decisional capacity, a Legally Authorized Representative (LAR) is needed to provide consent and uphold ethical standards.

In this 4-part series, learn about AI-driven methods that streamline data mapping and highlight critical issues that allow clinical teams to focus on what truly matters.

Explore six key ways laboratory data strengthens the clinical trial process, focusing on how RWD enhances patient recruitment, accelerates screening workflows, and improves overall study outcomes.

Patient-focused drug development (PFDD) is gaining traction as clinical trials increasingly prioritize patient perspectives alongside traditional endpoints.

Explore AI-driven automation and organ-on-a-chip technology to accelerate infectious disease research, improving vaccine and therapeutic development for emerging global health threats.

With each batch of cell and gene therapy product representing a wealth of lifesaving potential, this biopharma company needed the right packaging solution for its relatively new therapy applications.