Toronto, Ontario, Canada
+1 647-866-5477
Quality. Compliance. Privacy. Simplified.
AVIC Solutions delivers expert Quality Assurance, Data Privacy, AI Governance and Information Security consulting tailored to pharmaceutical, biotechnology, SaaS, and clinical research organizations. We specialize in GCP/GMP, ISO standards, Cybersecurity, Data Privacy and AI-powered compliance automation.
Strategic solutions that drive compliance, growth, & operational excellence.
For Leaders: Whether you are preparing for an upcoming inspection, initiating a clinical trial, or expanding your commercial manufacturing capabilities — we provide the trusted support needed to meet ICH, ISO, FDA, EMA, Health Canada, and MHRA expectations. Let us help you reduce regulatory risk, streamline your quality systems, and maintain confidence from site to sponsor.
Certified ISO Auditors
GCP/GMP and CSV/GAMP 5 Compliance
End-to-End QMS Implementation
Inspection Readiness and Management
Certified Data Privacy & InfoSec Professionals
AI Automation for Compliance
AI Governance
Quality Management Systems (QMS)
Operational Quality Oversight
Who We Are
AVIC Solutions is a boutique consultancy with a seasoned Quality, Data Privacy, AI Governance, and Information Security expertise, spanning over 20 years managing compliance and regulatory operations in global pharma, biotech, and digital health industries. We deliver strategic, scalable, and simple solutions to complex compliance problems.
Our Promise
With over 20 years of global experience, AVIC Solutions helps companies stay inspection-ready, audit-proof, and aligned with the latest regulatory expectations — from pre-clinical R&D through commercialization.
Our Vision
To empower your business with integrated Governance, Risk, and Compliance (GRC) solutions – helping you make smarter decisions, proactively manage risks, and ensure regulatory compliance so you can focus on growth and resilience.
Founder’s Bio
Candice Green, MSc, is a certified ISO 9001 Lead Auditor, Data Protection Officer (DPO), CIPP/E, and global GxP consultant with a strong background in molecular biology, biochemistry, data governance, quality management, and regulatory strategy. Her experience spans North America, Latin America, Europe, and Asia Pacific, and includes inspections by the FDA, Health Canada, PMDA, MHRA, NMPA, and EMA. She has led quality operations, information security operations, AI governance programs, and inspection readiness and management for early- to late-stage clinical trials as well as commercial pharmaceutical launches.
Quality & Information Security
ISO 9001 | ISO/IEC 27001 | ISO/IEC 27002 | ISO/IEC 27701 | ISO 22301 | NIST Cybersecurity Framework | NIST SP 800 series
Global Data Privacy & Data Protection
EU/UK GDPR | HIPAA | PIPEDA | CCPA/CPRA | LGPD | EU–U.S. Data Privacy Framework
Governance Driven Compliance
Clinical, GxP & Regulated Systems
ICH E6 | ISO 14155 | FDA 21 CFR Part 11 | FDA 21 CFR Part 50 | FDA 21 CFR Part 56 | GAMP 5 | CSV/CSA | EU Annex 11 | EU Annex 21 | EU Annex 22
AI Governance
EU AI Act | ISO/IEC 42001 | ISO/IEC 23894 | NIST AI Risk Management Framework | OECD AI Principles | FDA AI/ML SaMD Guiding Principles
Why Leading Organizations Choose Us
We understand the pressure to stay audit-ready while managing timelines and budgets. Our team integrates seamlessly with your operations to build right-sized compliance strategies without overcomplication. From site audits to trial master file oversight to computerized system validation, we bring experience that speaks the language of science, compliance, and speed.
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