Cell and gene therapy’s popularity has grown exponentially in the past year. However, it’s important to understand how cell and gene therapy research is different from traditional drug development.
Breaking down barriers to participation in clinical research has long been a challenge, affecting every aspect of the industry. As
Recently, we discussed the importance of connecting with advocacy groups in order to create more trial diversity. As a result
To maintain Part 11 compliance, research sites must validate electronic systems storing FDA-regulated records, safeguarding data integrity and accuracy.
A key element to successful study startup is identifying efficiencies to help meet critical milestones. Engaging with research compliance experts
Engaging participants and creating a positive experience throughout your clinical trial increases protocol compliance, participant retention, and referrals.
Budget negotiations reveal hidden costs and extended timelines, underscoring the importance of efficient processes for clinical trial success.
In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building an effective feasibility process, including
In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building an effective feasibility process, including
While the clinical research industry has developed innovative therapies and devices to serve patients all over the world, the industry
Patient centricity has long been a key goal in healthcare, as well as in clinical research. Sponsors want their participants
Centralizing subject binders and SOPs in an eRegulatory system streamlines remote monitoring, ensuring secure access, compliance, and future-ready workflows.
