Common mistakes, best practice and audit tips. The Qualsys service team run through how to build a clean and compliant document stack to show your MHRA auditor.
Every drug, device & clinical company wants to predict how regulations will impact their future processes. Here are 5 MHRA and FDA changes you need to know about in 2019
Validation costs putting your business off implementing a desperately needed integrated quality management system? Here's how our 5 step validation process genuinely makes it pain-free, efficient and easy to maintain.
BAP Pharma sources medicinal products from around the world. That means due diligence, strict quality control and consistent best practice. BAP Pharma's Head of Quality explains how EQMS by Qualsys became a 'second person' supporting his goals.
Not sure what an audit trail is or where to find one in Qualsys's software? Here's the what, how, where, when and why you need audit trails for GAMP, FDA and MHRA compliance.
Read how Well Pharmacy's audit team saved themselves a week per month and cut profit leakage by 25%.
Sodexo's EQMS Manager Rob Gibson explains why his pharmaceutical clients are 'raving' about Qualsys's software solution.
Find out how Qualsys's software helps you comply with ISO 13485:2016 Design controls.
Here are three mistakes to avoid when planning your Trial Master File.