There is nothing more rewarding than bringing new therapies to patients. The IQS Consulting team of cGMP, Quality System, and CMC experts will assist your team on this journey. Whether your need involves Quality System alignment, auditing your key suppliers, selecting and working with your CDMOs, determining if your team is inspection ready – we are keen to help. Development stage companies call on our experts for:

• Site assessments for GMP manufacture
• Pre-Approval Inspection Readiness
• Supplier cGMP Audits
• Qualified Person (QP) Audits
• CDMO Assessment and Selection
• Quality Assurance Support
• Quality Systems Development, Implementation, and Improvement
• CMC Support – Combination (Drug/Device), Inhalation, and Parenteral Products