
Navigating the new era of GxP compliance with smarter digital workflows
Tuesday, June 16 at 16:00 BST | 17:00 CEST | 11:00 EDT | 08:00 PDT
Pharmaceutical and biopharmaceutical teams working in GxP‑regulated environments are navigating growing regulatory demands, legacy system limitations, and the need to modernize digital workflows while maintaining strict compliance with global standards such as 21 CFR Part 11, Annex 11, and broader GxP frameworks. As these pressures intensify, many organizations are seeking clearer strategies and proven approaches to evolve their systems without introducing compliance risk.
In this SelectScience® webinar, GxP experts Ankita Dhar and Jenny Lesinski from Revvity Signals will share practical strategies for streamlining compliant workflows, strengthening data integrity, and reducing the burden of computer system validation using a portfolio of solutions including Signals One™. They will also spotlight real-world stories that illustrate the challenges teams face, from managing complex validation cycles to adapting to shifting regulatory expectations, and how those organizations successfully addressed them.
Whether you are exploring new digital solutions or looking to optimize existing regulated workflows, this session will equip you with actionable insights to enhance compliance, improve efficiency, and support long-term operational excellence.
Certificate of attendance
If you attend the live webinar, you will automatically receive a certificate of attendance, including a learning outcomes summary, for continuing education purposes.
If you view the on-demand webinar, you can request a certificate of attendance by emailing editor@selectscience.net.
Webinar details
- Cost: Free to attend
- Location: Online
- Duration: 60 minutes
Registration is required to secure your place. If you register but can’t attend live, you will receive a link to the on‑demand recording once it becomes available.
Speakers



Who should attend?
- Biopharmaceutical R&D professionals
- Biopharmaceutical contract research organizations (CROs)
- Biopharmaceutical contract development and manufacturing organizations (CDMOs)
- Quality control professionals
- Lab informatics managers
- Digital transformation leads
- Operations directors
What will this webinar cover?
- The core challenges of operating in GxP‑regulated environments
- How modern digital platforms can streamline compliant workflows
- Revvity Signals’ approach to GxP‑focused innovation
- Insights into the real‑world experiences of your peers



