Here are some really great free resources for you to help level up your knowledge base

We talk a lot about 21 CFR (especially part 11) in clinical research - there's so much more to it than meets the eye

Don’t make these mistakes. Top features you need to look out for when implementing your eTMF system

Sites are absolutely critical to the success of any trial. Here's how our Trialflare features help your site succeed

Strong ethical guidelines protect participants in trials - but when do they come into play?

Demonstrating compliance in your clinical trials conduct should be straightforward - here's how to compile the most important information for audit review

Engagement drives compliance! How do you keep participants engaged in your human trials?

In this tech-dominant era, there are plenty of ways we can use it to better engage with participants

Human trials in the UK typically need to be greenlit by the National Health Service (NHS). Avoid delays and constant changes by checking off some of these key items

Keeping documentation up to date, fully transparent and up to regulatory standards can be tricky. Here are some of the most essential trials documents you should be aware of

Human trials often come with expectations of making some sort of claim. While that's very important, data quality is fundamental

Sites, sponsors and end-users... making EDC platforms work for everyone? Here are the essentials...

Is anonymity always required? How do you retain participant data rights in trials?

Are you aware of clinical trial phases? The concept and purpose of phases has evolved significantly over the last century

You need to conduct research across many borders in diverse populations and adhere to international ethical standards and practices. Here's how...

The term "GDPR" can incite fear and worry in the minds of many researchers. Here's what GDPR means for your human participant research

Regulatory authorities outline in great detail how a trial should be properly conducted. With technology, eSource can make things much easier for you

The DCT approach is not for everyone, but if you're looking to make the switch, what are the key questions you should be asking yourself?

If you're conducting human participant research in the UK, you will need to be aware of IRAS

There are many ePRO systems available with many offerings, but what are the most useful features that will help you?

Standard Operating Procedures (SOPs) ensure proper trial conduct to regulatory guidelines and frameworks - how should you work yours according to best practices?

An in-depth look at the top 10 most communicated points surrounding data collection in human research

Protecting your data should be a top priority - whether it's sensitive intellectual property or private health records

Data collection comes with many challenges - whether you're using traditional methods, hybrid or all-in-one software approaches. Here are the most communicated issues from researchers worldwide

Addressing one of the most fundamental questions in data collection. Is my work even 'research'?

What are the obstacles to success in your trials? 8 things you need to be aware of

The two main types of trials - Intervention and Observational. Here are the differences and what they mean for you

A simple and instrumental way to assess cognitive ability in a variety of situations

How one incredible black woman, Henrietta Lacks (HeLa), played her part in changing the world of biomedical research

Both blinded and un-blinded trials need fair group allocation. Here's how you can manage proper randomization in your trials

How can we best protect participant identities in research? Here are our top tips and methods

Automate your anthropometric data collection with our Body Mass Index (BMI) data type

Collect nutritional intake data from your participants. More than 3,000,000 international food and drinks items, or customise your own

Covering the basics of electronic and digital signatures in the USA/UK and EU. Did you know there was a difference?

Image uploads can improve compliance, participant monitoring and reduce the burden on participants. Here's how

Finding the right cohort for your trial can be difficult, but honesty and transparency are a must - Participant Information Sheet (PIS) essentials

Cognitive tests are essential tools in the assessment of brain health and disease, but why? and which ones should we be using?

Read our quick guide on two-factor authentication (2FA) to help protect your research team and participants

Our easy 2-step guide to getting your organisation set up securely with Single Sign-On (SSO)

We've come a long way in the last two years, but what lies ahead for COVID-19 and trials research?

How did one man shape the future of clinical trials research?

What is the future of clinical trials process and methodology? Can DCTs help pave the way to better trials?