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Driving quality excellence in 2021
Eric Stoop, CEO at EASE Inc – a developer of plant floor audits and insights software in the US – provides his top five tips to help manufacturing businesses overcome the obstacles posed by Covid-19.
- United Kingdom
External Auditing During The Pandemic - What Are The Key Factors?
This event, part of the CQI Scottish Region "remote" programme for 2021, is hosted by the West of Scotland Branch.
- United Kingdom
CQI Derby & Nottingham: Constructing the future of quality
An opportunity to learn the approach being taken to deliver the future of quality within one of the UK’s leading construction companies.
- United Kingdom
Making the most of your IRCA membership
Being an IRCA member makes you part of a unique network of thousands of professionals working in auditing. This webinar will explore the benefits of membership.
- United Kingdom
Creating Value For Your Customers Through a Quality Management System
Discover how to create value for your customers.
- Worldwide
Launch event: a new CQI Network in the Caribbean
Are you based in the Caribbean? Would you like to find out how the CQI can support you and how you can become part of a new network?
Dealing with time pressures
In our latest dilemma, find out how to avoid delays with audits and ensure they’re delivered within the audit plan’s designated timeframe.
- United Kingdom
CQI Leicester & Coventry - Book Club - "Turn the Ship Around"
A new CQI format by the Leicester & Coventry Branch, a Book Club based on "A True Story of Turning Followers Into Leaders".
- London
Choosing your CQI grade and how to apply
Gain practical advice to give your application the best possible chance of success.
24 hours
MD-QMS Comprehensive EU Medical Device Regulation 2017/745 (EU MDR) Practitioner (Medical Device – Quality Management System)
This course aims to provide learners who have an existing, basic knowledge of, or experience in, quality management in the Medical Device Industry with an in-depth understanding of the application under the European Union’s Medical Device Regulation (EU-MDR 2017/745) Regulation.