Why should we work with QA&C Consulting?

With QA&C Consulting, you gain a trusted advisor dedicated to ensuring compliance, improving quality performance, and supporting your organisation’s continuous growth.

You will be supported directly by a certified QA consultant (CQA) with over 20 years of hands-on experience in regulatory compliance, ISO 13485 implementation, and medical device quality management systems. My practical, real-world approach ensures that your quality processes are effective in daily operations, fully compliant with FDA and ISO standards, and always audit-ready.

Key Advantages:

• Transparent and affordable pricing – No hidden fees. Services are tailored to suit organisations of all sizes, from startups to established enterprises.

• Operational efficiency – Engagements are conducted with focus and precision, no wasting time on idle convestaions, avoiding unnecessary meetings or overutilisation of company resources.

• Outcome-driven delivery – Through a streamlined “set-and-execute” approach, you define the objectives, and I manage the rest to ensure timely, compliant results.

• Strict confidentiality – All projects are managed under a confidential, trust-based partnership focused on mutual goals and long-term relationship and success