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Good Auditing Practices, Making the Most of Your Internal Review


FDA regularly audits facilities for compliance with GMPs, shouldn’t you?

Regular and formal internal audits provide a clear, unbiased view of your facility operations and uncover challenges that must be addressed. No matter your FDA regulated industry, having a formal, thorough and documented audit plan will streamline your audit processes and ensure replicable efforts that track progress.

Learn the fundamentals of developing an audit program with EAS Consulting Group’s seminar Good Auditing Practices. This eight-hour seminar will detail design and implementation strategies to ensure your audit program meets the high level of detail expected by FDA field auditors.

You’ve designed a robust GMP system for your manufacturing facility. Shouldn’t your audit program have the same level of detail?

All seminar registrations are per person.