"At Quality CQV, we specialise in delivering tailored quality control and validation solutions that fit your pharmaceutical project’s exact needs. Unlike one-size-fits-all providers, we think outside the box to solve complex challenges, ensuring your processes are efficient, compliant, and innovative. Partner with our experienced team to bring your project to life with confidence and ease. Ready to elevate your quality assurance? Let’s connect and create a unique solution that drives your success."
We believe in what we do and that’s why we're committed to helping more people. To make sure the process is as seamless as it can be, there are lots of ways we can work together. Our range of services can be tailored to suit your goals, your business, or your project. Don't forget, we specialize in thinking outside-the-box. If you're looking for new ways to bring your project to life, then have our team design a solution that's truly unique.
Our Services
Pharmaceutical
30+ years delivering commissioning, qualification and full life cycle validation for pharma and medical device facilities (IQ/OQ/PQ, FAT/SAT, CSV, Design History Files). Experienced with MHRA/EMA GMP, FDA.
Available for 2–6 month and and longer ad‑hoc projects across the UK
Recently contributing as a CQV Engineer at large Pharma company in the North of England, focusing on commissioning, validation, verification, and user acceptance testing. Skilled in ensuring compliance and efficiency in quality assurance processes, with expertise in executing commissioning, validation processes and delivering results. Demonstrating a collaborative approach to ensuring systems and processes meet regulatory standards and business goals.
Medical Devices
Preparation and submission of the documentation required for IEC 60601 – 4.1 Edition certification.
Generation of – Risk Management File including: Risk Management Plan, Risk Analysis, Usability Engineering File & Risk Management Report.
(IEC - 13485, 14971, 60601, 62366, 62304)
Generation of the Design History Files
Including the following:
Validation and Verification of the products.
Risk Management Planning, Design Inputs, Design Outputs, Design Verification, Design Validation, Software Validation.
Material Analysis
We provide fast, reliable non-destructive testing (NDT) analysis to detect defects, assess integrity, and extend the life of critical assets—without harming components or interrupting operations.
Using advanced methods (ultrasonic, radiography, eddy current, magnetic particle, and visual inspection) and ISO-compliant reporting.
Our expert technicians deliver accurate findings, actionable recommendations, and traceable documentation to support safety, quality, and regulatory needs.
Discover Our Unique Services
Tailored Quality CQV Solutions
We customize our quality control and validation services to fit your project's exact requirements, ensuring efficiency and compliance.
Innovative Problem-Solving
Our team excels at creating out-of-the-box solutions that address complex challenges in pharmaceutical quality assurance.
Collaborative Partnership Approach
We work closely with your team, adapting to your business goals to deliver seamless integration and support.
Expertise You Can Trust
With years of industry experience, Quality CQV is your reliable partner for quality and compliance excellence.