FDA & Global Regulatory Training Support » » »
We provide cost-effective, in-house training support to help biotechnology companies and clinical research teams meet FDA and Global training requirements.
Our Most Popular Training Topics Include:
» FDA Quality System Regulation - cGMP/QSR 21 CFR Part 820
» FDA Inspection Readiness: Prepare Your Company Before FDA Arrives
» International Quality Systems - Current ISO 13485
» 21 CFR Part 11: Requirements & Validation Process Overview
» Risk Management for Medical Devices - Current ISO 14971
» GLP & GxP Overview - For Academic Research PIs & Their Lab Teams
» Clinical Trial Monitoring: Best Practices For Optimal Outcomes
» Preparing For FDA Inspections: Gap Assessments & SME Readiness
» Preparing For An FDA BIMO Inspection: Is Your Study Team Ready?
Please contact us at email@example.com to let us know what your training needs are. We'll customize a cost-efficient training program for your R&D/QA team, your Institutional Review Board (IRB) and / or your clinical research team.