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Blog: Why 2025 is the year businesses need to think different
Halfway through one of the most tumultuous decades in recent history, will 2025 finally be the year things settle down? Well, according to the latest Ideagen report, it’s less settled, more poised to pounce.
News: Ideagen’s EHS software top for AI capability
According to prestigious independent research and advisory firm.
White paper: Elevating EHS performance through continuous improvement
Our latest white paper distills the expertise of industry leaders to guide you in transforming compliance into a strategic advantage.
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CAPA For Medical Devices – ISO 13485 Guide
Ensure regulatory excellence with Ideagen's CAPA guide for medical devices. Streamline compliance processes and elevate product safety standards.
Ideagen QMS for ISO 13485
Ensure compliance with ISO 13485 by implementing a robust quality management system tailored to medical device manufacturing and services.
guide
The necessity of GAMP5 2nd Ed. and the FDA’s CSA guidance
guide
European medical device regulation checklist
white paper
Risk-based oversight: How to mitigate future risks before they happen
white paper
Unlocking safety intelligence to make compliance easier
guide
Regulatory compliance in manufacturing: AS9102
Webinar
Safety leadership lessons of Shakespeare's works
Webinar
Mastering stakeholder engagement in internal audit
Webinar
Top management commitment to quality
e-book
Simplifying retailer audits in the food and beverage sector
white paper
Agile auditing: How to plan, communicate and embed
guide
What will the future of aviation look like?
white paper
Does Ideagen Quality Management adhere to Title 21 CFR Part 11?
white paper
Building a resilient safety culture
white paper
Understanding ISO 13485
white paper
Four benefits of adopting an integrated approach to CAPA
Blog
Why are most restatements negative? Behavioral accounting at work
Blog
2024 Audit Committee Transparency Barometer
Blog