Webinar

The webinar will cover strategies for new hires joining the clinical trial industry and key topics to include in your onboarding plan.

Representatives from the Advarra Site-Sponsor Consortium will discuss a standards-based integration and automation of research technology.

Explore regulatory frameworks applicable to research involving cosmetics, conventional foods, and dietary supplements.

Critical insights and key considerations for selecting the best regulatory pathway to ensure success for new drug application submissions.

Explore the current regulatory landscape governing mHealth and virtual trial applications in clinical research.

Explore research programs' case studies where engagement strategies increased recruitment, reduced deviations, and achieved enrollment goals

In this webinar, we outline the Whole Product Approach, a comprehensive strategy focusing on all aspects of the user and site experience.

This webinar covers strategies for adapting your training program using in-person, live virtual, and virtual/asynchronous approaches.

Explore strategies for advancing investigational new drug (IND) submissions and a comprehensive guide through Phase I of the IND journey.

The webinar dives into current QMS challenges and recommend strategies to advance successful QMS programs across your enterprise

Dive into current regulatory challenges your teams face and recommends strategies to expedite go-to-market plans across multiple activities

This webinar offers three strategies to check and reduce blind spots regularly to improve compliance oversight.