Introduction – Clarity for Regulated Industries
Every regulated industry faces unique calibration challenges. Aerospace manufacturers must align with FAA and AS9100; medical device makers must meet FDA and ISO 13485; automotive producers follow IATF 16949 standards.
ICS understands these differences — and we’ve built this comprehensive FAQ resource to help your team stay compliant, audit-ready, and confident in every calibration decision.
This downloadable guide answers the most common questions about industry-specific calibration, traceability, and documentation, helping Quality Managers, Compliance Officers, and Engineers understand how ICS supports sector-specific requirements.
What’s Inside the FAQs Document
- Answers to top calibration and compliance questions from aerospace, medical device, and automotive industries.
- Clarification on standards and traceability, including ISO/IEC 17025, NIST, and industry-specific frameworks.
- Guidance for audits and inspections — what documentation is needed and how ICS helps clients stay audit-ready.
- Information on on-site and multi-facility calibration programs for global and multi-location operations.
- Practical insights from ICS experts with decades of calibration experience across regulated environments.
Why Download This FAQ Document?
ICS doesn’t just calibrate instruments — we help clients maintain compliance, pass audits, and operate with precision.
Our ISO/IEC 17025-accredited services are designed for industries where accuracy and documentation aren’t optional — they’re essential.
By downloading this FAQ guide, you’ll learn:
- How ICS tailors calibration to your industry’s regulations.
- What makes traceability vital for quality assurance.
- How to prepare your next audit with confidence.
