EMEA Office
Kantersteen 47
1000 Brussels
Belgium
Sep 15, 2026 11:00 AM (CEST)
Don’t wait until your 2027 audit is on the calendar to find out where the gaps are.
Recent Warning Letters and inspection findings continue to reveal recurring gaps in quality and compliance. And when processes, data, and responsibilities are managed in silos, those gaps can be difficult to spot until an audit puts them under the spotlight.
So, how can you get ahead? In this CaseLab, quality and compliance expert Antiksha Joshi explores what recent regulatory findings can teach us about audit readiness and, more importantly, what organizations can start doing now to prepare for 2027.
Join us to learn from real regulatory findings, assess where your own gaps might be, and see how Scilife can help you stay ready before your next audit is even on the calendar.
Antiksha Joshi is a pharmaceutical quality management expert with more than two decades of experience helping life science organisations strengthen compliance and streamline operations. She specialises in supporting small to mid-sized biotech, clinical, and manufacturing teams to build practical quality systems that not only meet regulatory requirements but also improve productivity and operational flow.
Account Executive
Scott Townsend is an Account Executive at Scilife with a background in quality systems and compliance. His hands-on experience across quality assurance, supplier compliance, and digital quality implementation gives him a practical understanding of the challenges organizations face when managing risk, documentation, and regulatory requirements. At Scilife, he helps life sciences companies streamline quality processes, strengthen compliance, and drive operational efficiency to achieve their business goals.
EMEA Office
Kantersteen 47
1000 Brussels
Belgium
US Office
Scilife Inc.
228 E 45th St. RM 9E
New York, NY 10017
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EMEA Office
Kantersteen 47
1000 Brussels
Belgium
US Office
Scilife Inc.
228 E 45th St. RM 9E
New York, NY 10017
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