Richard Forsyth
Principal Consultant
Forsyth Pharmaceutical Consulting
Internationally recognized expert in cleaning validation remediation with multinational clients, numerous publications, and extensive speaking engagements. Pioneered new industry approaches to visual residue limits, equipment hold-times, and use of ADEs for acceptance limits.
Extensive experience (30+ years) in process validation, QC, QA, analytical and bioanalytical test method development, validation and document preparation in commercial and R&D laboratories.
DAY 1: October 1st, 2025
SESSION: Establishing Limits & Acceptance Criteria
◆ Basics of limit parameters.
◆ Limit calculations.
◆ Practical considerations in applying limits / acceptance criteria.
SESSION: Visual Inspection in Cleaning Validation
◆ Regulatory expectations for visual inspection.
◆ Establishing visibility limits for residues.
◆ Case study: Challenges and best practices in visual inspection.
