WOMAN-OWNED • SOUTHERN CALIFORNIA

Quality systems
built for excellence.

Expert AS9100 and ISO 13485 consulting for aerospace, medical device, and manufacturing organizations. Over 50 years of combined experience delivering certification success and sustainable quality programs.

AS9100 Lead Auditor Certified
ISO 13485 Lead Auditor Certified
50+
Years Combined Experience
100%
Certification Success Rate
Woman
Owned & Operated
Tailored
Solutions for Every Client
WHO WE ARE

A partner invested in your long-term success.

C&C Consulting is a premier, woman-owned quality management consulting firm based in Southern California. With over 50 years of combined experience in the manufacturing industry, we specialize in AS9100 and ISO 13485 quality management systems.

We provide expert support for aerospace, medical device, and manufacturing organizations seeking to implement, maintain, and continuously improve compliant quality programs.

Clear Communication
We keep you informed at every stage with transparent reporting and proactive updates.
Competitive & Fair Pricing
Premium expertise without the premium agency markup. Value-driven engagements.
Tailored Solutions
No cookie-cutter programs. Every engagement is designed around your unique operations and goals.
WHAT WE OFFER

Flexible consulting solutions

Choose the engagement model that matches your team's capacity and goals.

OPTION 1

Implementation + Client Maintenance

We implement your complete Quality Program and equip your team with the tools, documentation, and knowledge required for independent ongoing maintenance.

OPTION 2

Full-Service Implementation & Maintenance

We manage both the initial implementation and all ongoing maintenance activities. Your quality system stays compliant and effective with minimal internal burden.

OPTION 3

Consulting & Program Enhancement

We collaborate with your existing team to optimize and elevate your current quality program — providing expert guidance while you retain day-to-day ownership.

HOW WE WORK

Our proven methodology

A structured, transparent process designed to deliver certification success and lasting operational improvement.

01
Initial Review & Gap Assessment

We evaluate your existing quality management system against AS9100, ISO 13485, and ISO 9001 requirements to identify gaps, risks, and opportunities.

02
System Development

We create or refine your Quality Manual, procedures, work instructions, forms, and documentation aligned with regulatory and business requirements.

03
Employee Training

Practical, role-specific training ensures your team understands responsibilities and can confidently execute new processes and quality objectives.

04
Internal Audit Support

We conduct or facilitate internal audits to verify compliance, surface improvement opportunities, and prepare your organization for certification and customer audits.

05
Management Review & Corrective Action

We support management reviews, corrective action programs, risk-based thinking, and continual improvement initiatives to keep your system effective.

06
Certification Audit Preparation

We partner closely with your team and coordinate with your chosen registrar to ensure a smooth, successful certification audit outcome.

NEXT STEP

Let's build your
quality foundation.

Based in Southern California. Serving aerospace, medical device, and precision manufacturing clients nationwide.

We typically respond within one business day.