Designing & Constructing Life Sciences Facilities with FDA Readiness at the Core
Time: 2:10 pm
day: Conference Day Two
Details:
- Presented from the Client Perspective and from a Consulting/Design/CM Perspective
- Learn how to integrate FDA and cGMP requirements into facility design from day one inception through startup, ensuring the design basis and infrastructure aligns with regulatory guidance
- Analyzing insights from past inspections and audits to anticipating trends with recent Administrative and Regulatory directional shifts to shape smarter, faster, and more compliant project delivery, avoiding common pitfalls and delays
- Engaging qualified cross-functional teams early including stakeholders, engineering, quality, regulatory, and operations—to design and build facilities that are geared for inspection-readiness while being patient-focused
Speakers:
