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In this insightful webinar, David Graham, Senior Counsel at Gardner Law, explores the critical role documentation plays in litigation and regulatory compliance for FDA-regulated companies. Drawing on over 35 years of litigation experience in the medical device, pharmaceutical, and food industries, David explains why what’s on file could make—or break—your case. In Part 1 of this two-part series, David covers: ✅ Why documentation is essential for business operations, regulatory audits, and litigation defense ✅ The legal concept of spoliation and how mishandled documents can lead to sanctions or adverse findings ✅ How to protect attorney-client privilege and work product in company communications ✅ Strategies for safeguarding confidential information ✅ Best practices for document retention policies and employee training Whether you work in legal, compliance, quality, or executive leadership at an FDA-regulated company, this webinar provides practical tips for minimizing document risk and strengthening your company’s litigation readiness. 👉 Don’t miss Part 2, where David discusses how to avoid creating “bad documents” and handle problematic communications in emails, texts, and internal records. 📥 Slides and resources available at Gardner.law #FDA #Compliance #MedicalDevice #Pharmaceutical #Litigation #LegalRisk #Documentation #AttorneyClientPrivilege #GardnerLaw