Reliable FDA Compliance & Quality Experts
With 20+ years of expertise across pharma, biotech, PET, supplements, and cosmetics, ICGMP provides top-tier regulatory guidance, risk management, and audit readiness.
Area of Expertise
We conduct FDA-style quality audits and risk assessments to help organizations identify noncompliance, prevent product defects, and mitigate the risk of regulatory actions such as Untitled and Warning Letters, recalls, seizures, injunctions, debarment, and criminal prosecution—outcomes Dr. Inokon successfully navigated during her FDA tenure. With your partnership, we are committed to delivering expert guidance on FDA regulatory standards for pharmaceutical products.
Regulatory Audits & Risk Assessment
We offer expert reviews of regulatory action classifications and assist companies develop effective Corrective and Preventive Action (CAPA) strategies. Our focus extends beyond remediation to building sustainable quality systems that consistently withstand inspection.
CAPA & Quality Review Oversight
ICGMP will assess your current training programs to identify areas for improvement in your team’s Good Manufacturing Practices (GMP) knowledge. We combine regulatory expertise with leadership development to cultivate confident, audit-ready professionals.
GMP Training & Workforce Development
FDA Pharmaceutical Inspectorate, Level III Drug Certification
FDA Level III Certification in Drugs was awarded by the Certification Board for successful completion of advanced training in pharmaceutical inspection and compliance enforcement.
Leadership Certifications
Dr. Inokon is a self-starter with a people-first mindset, always chasing growth. To stay sharp, she’s earned training certifications from USF MUMA College of Business.
