Courses #2 Days - Eventura.site

FDA Inspections and Audit Readiness Course

The DHF, Technical Documentation - Similarities, Differences and the Future

Live In-Person Seminar on Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities - Richmond, VA

Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities

Writing SOP’s and Work Instructions that Really Work

Validating and Auditing Cloud, SaaS, IaaS, PaaS Systems - Tech & Validation Trends for FDA Compliance

Supplier And Contract Manufacturer Management

SaMD Masterclass - Validation, Change Management, Cybertechnology, and Best Practices

TECHNICAL WRITING MASTERCLASS IN THE LIFE SCIENCES

Analytical Instrument Qualification and Excel Validation - Preparing for FDA Audits

GLP LABORATORY COMPLIANCE DOCUMENTATION AND RECORDKEEPING

OOS And OOT Investigations Course - Best Practices, Key Components and A Comprehensive Review of The FDA Requirements