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What is the medical device technical file? What should it contain and how should it be structured? And is it e...
What is the medical device technical file? What should it contain and how should it be structured? And is it e...
For some companies simply managing their documentation is enough to support their business goals. But others n...
MasterControl is an eQMS system that supports the quality management of complex and highly regulated life scie...
Cambridge, UK, 22 October 2024: Cognidox, a leading provider of document management solutions for high-tech, m...
What’s wrong with SharePoint, anyway? Why shouldn’t it be used as a document management system (DMS) for a gro...
Having a repeatable procedure for Corrective and Preventive Action (CAPA) is a key FDA requirement for medical...
An Electronic Document Management System (EDMS) is a software that centrally stores and organises documentatio...
Would your business benefit from using electronic signatures within your digital quality management system (eQ...
The FDA’s new QMSR is dropping the reference to the DHF (Design History File) when it takes effect in 2026. Bu...
Medical device audits can be a source of stress for developers and manufacturers. But what exactly are the aud...
In the biotech scale-up space, your data and documentation are often the extent of your IP. That’s why you nee...
With complexity and costs rising, fabless semiconductor companies need to do all they can to keep their flow a...
Q-Pulse is a quality management system from Ideagen that helps organisations manage compliance, quality, and s...
EU Annex 11 provides guidelines for the use of computerised systems in ensuring Good Manufacturing Practices (...
ISO 14971:2019 defines the international requirements of risk management systems for medical devices. How does...
Dubbed the 'combination of money and molecules', Biotech is a famously hard sector in which to find and fund s...
Post-Brexit, there is still confusion about the future use of the UKCA (UK Conformity Assessed) markings and w...
WTH is FDA 21 CFR Part 11? That’s a question many life science developers wanting to access the US market must...
Transferring data to a new electronic Quality Management System (eQMS) can seem like a daunting prospect. Here...
On the 16th of May, Cognidox welcomed nearly 100 attendees from across the high-tech, medical device, and phar...
It’s the job of your corrective action process to identify and eliminate the systemic issues that will prevent...
Managing the integrity and accessibility of a PSMF (Pharmacovigilance System Master File) is a key challenge f...
What does it mean to 'control documents'? And who needs a formal document control system to manage and optimis...
Managing deviations from standard operational procedures is critical to product quality and regulatory complia...
The Cognidox team is delighted to announce we will be hosting CogniCon 24 on 16 May 2024. This is a networking...
Google Drive is a cloud-based program that allows you to create, edit, store, and share documents. Many busine...
ICH Q8 R2 are international guidelines for ensuring Quality by Design in pharmaceutical development. Here’s wh...
How do you log and deal with non-conformities so that faulty products don't end up in the hands of customers? ...
A Trial Master File (TMF) is a comprehensive collection of documents that ensures the conduct of your clinical...
Data integrity is central to the safe development and manufacturing of every life-science product on the marke...
Navigating the complexities of ISO 13485:2016 can seem daunting, but understanding its requirements is crucial...
The case for ditching paper based QMS (Quality Management Systems) can seem like a no-brainer. But faced with ...
In 2008, the ICH Q10 Pharmaceutical Quality System (PQS) guidelines introduced a comprehensive model for an ef...
Cognidox and Qualio are both digital quality management systems (QMS) with a focus on the life science and med...
In medical device development, two critical stages of the design process are often confused: design verificati...
What if you could gain approval to sell your medical devices anywhere in the world, by completing a single, re...
What’s the cost of quality? Can it, like QM guru Philip Crosby argued, really be free? Like most things in bus...
Controlling and documenting IQ, OQ and PQ effectively is a complex and time-consuming process for life science...
Cognidox are delighted to announce the release of our new DocuSign e-signature integration. The new plug in is...
Change control in life science development is critical to ensuring the safety of patients. Having a formal pro...
Chip designs are becoming more complex and expensive to develop, verify and validate. Opportunities for fables...
Clinical research demands strict GCP (Good Clinical Practice) compliance. But many institutions stuck with out...
At last! It’s happened! The FDA has announced the date for the publication of its new Quality Management Syste...
Transferring design to production is a process that can be fraught with risk for medical device developers. Ho...
There are many reasons why organisations need to document their SOPs. From ensuring uniformity in end products...
There’s plenty of document management and file-sharing software available on the market, but not all of it is ...
Of all the quality management ‘gurus’, the late Philip Crosby is one of the most readable. In his book ‘Qualit...
The regulations and literature surrounding medical device development are packed with acronyms and technical t...
Will a phase gate process hold back or enhance your new product development? What are the pros and cons of sta...
A Quality Management System (QMS) is a requirement for medical device developers across the globe. But should ...
How can you help your business evolve its mindset to achieve the most instinctive, frictionless and effective ...
If you’re a tech start-up or growing SME looking to implement an enterprise-grade file-sharing solution and co...
The FDA’s Quality System Regulation (QSR) for medical device manufacturers is commonly known as FDA 21 CFR Par...
The medical device development process is typically broken down into five distinct phases. Each one requires i...
SMEs creating a digital Quality Management System (QMS) will often reach for the most familiar tools to build ...
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