Regulatory Compliance Videos

1. Sticky Situations: Tackling Residue Inside The Cleanroom With Dave Nobile 8/24/2026

   Learn how to effectively manage chemical residue buildup in cleanrooms through proper solvent selection, dwell time, and mechanical removal to support regulatory compliance.

2. The Story Behind MIDBA: An Exclusive Interview 8/20/2026

   A new regulatory framework reduces PK bridging study needs, helping sponsors streamline device transitions, lower costs, speed up timelines, and boost regulatory predictability for combination products.

3. Supporting Digital Documentation With AI 8/6/2026

   In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists talk about how the AI layer fits in to support verification and validation as well as trending the data, but address what guardrails are needed, including human oversight in data review. They also address what happens if AI misses something.

4. Clear Data Handoffs And Cross-functional Teams 8/6/2026

   In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists talk about maintaining clean data handoffs when there are multiple platforms involved to avoid gaps in accountability. They also discuss how cross-functional teams can better support regulatory compliance.

5. Paper To Digital Transition And Paper Fallback 8/6/2026

   In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” experts discuss common compliance gaps when transitioning from paper-based or hybrid documentation systems to digital systems, including: incomplete system validation, poorly defined user requirements, training and, change management. The panelists also discuss the mindset that may be holding them back from transitioning and where it is important to have a paper fallback.

6. Changing Inspection Readiness Into Continuous Improvement 8/6/2026

   In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation” our panelists talk about transitioning from the old approach of preparing for an inspection to continuously being ready for the inspection, including how leaders can get their team on board.

7. Real-Time Deviation Management 8/6/2026

   In this segment from the Pharmaceutical Online Live event, “Building Inspection Ready Systems With Digital Documentation,” panelists discuss deviation management, CAPA and root cause analysis change when documentation becomes real-time and data driven.

8. Safety Of Injectables: Ensuring Purity Via Endotoxin Testing 7/28/2026

   Advance pharmaceutical quality and sustainability by adopting recombinant factor C testing for reliable, animal-free endotoxin detection.

9. Ask Us Anything: Anmaris Torres On The First Steps In Process Transfer 7/23/2026

   Anmaris Torres, Process Engineering Team Leader, on why a process transfer starts with a conversation across departments to figure out how to cut cycle time before commercial production begins.

10. Ask Us Anything: Miles Blackburn On Advances In Flow And Radical Chemistry 7/23/2026

    Miles Blackburn, Associate Director of Chemistry at Snapdragon Chemistry, on why the biggest payoff of flow and radical chemistry is speed — processes that scale fast enough to get intermediates and APIs delivered on a clinical timeline.