Blogs and News
Discover our latest news and blog articles, dedicated to demystifying drug development, medicine, clinical research, and ethics.
How planning to fail can help biotech overcome clinical trial hurdles
As a sponsor, you are aiming for success with your clinical trial. Paradoxically, one of the best ways to achieve this might be to plan for failure. Here we look at some of the stumbling blocks you can anticipate in order to avoid them
Patient centricity in clinical trials
Clinical trials are a vital step in the process of getting an intervention to the patients who need it. Putting those patients first, from the start of the design process to reporting the results, can help you succeed. Here we share insights from 25 years of clinical trials, to help you improve patient centricity.
Free FSP Model eBook for Biotech Clinical Trials | Siron Clinical
The FSP model eBook for biotech clinical trials is now available from Siron Clinical. A comprehensive, experience-driven guide to building flexible, expert-led partnerships in clinical research.
Benefits of point-of-care clinical trials for sponsors
What if a clinical trial were integrated seamlessly into patient care, so each patient could get maximum benefit from the treatment on trial, while saving time and money? Point-of-care trials bring clinical research into everyday healthcare, and they have both advantages and challenges.
Siron Clinical at BioFIT 2025: Let’s meet in Strasbourg
We’re delighted to share that Siron Clinical will be attending BioFIT 2025 this December in Strasbourg.
Siron Clinical At The World Orphan Drug Congress Europe 2025
Siron Clinical will be participating in the World Orphan Drug Congress Europe 2025, held from 27 to 29 October at the RAI Congress Centre in Amsterdam.
AI tools for predictive patient recruitment and monitoring in clinical trials
Artificial intelligence (AI) promises efficiency, accuracy, and cost savings, but what can it actually deliver when it comes to clinical trials? Whether you’re in the design process of your clinical trial, working on regulatory submissions, recruiting participants, or collecting and analyzing data, there may be AI tools to help.
How site initiation visits work in clinical trials
To get the best start with a clinical trial, we carry out a site initiation visit (SIV). In this post, we look at what that entails and how we ensure it sets the trial off in a positive direction.
Clinical trial success depends on strong partnerships – here’s why
If you’re running a clinical trial, your partnerships could mean the difference between success and failure. Here we look at why and share tips for getting the most out of your collaborations.
Are You Heading to Amsterdam for the Clinical Outsourcing Group CRO Summit 2025?
From the strategic to the scientific, from AI integration to cross-functional collaboration, this year’s Clinical Outsourcing Group (COG) CRO Summit Europe in Amsterdam is set to tackle some of the most pressing challenges in clinical development today.
Clinical Trials News and Updates: 5 Tips To Stay On Top
Stay up-to-date with all the latest clinical trials news and updates without adding hours to your day. Here are five proven, time-smart ways to keep your finger on the pulse, from new regulations to emerging study data.
Difference Between Clinical Trials and Clinical Studies Explained: What Sponsors Need to Know
What’s the difference between clinical trials and clinical studies? The terms get used interchangeably all the time, but they’re not the same thing, and for sponsors, getting it wrong can be costly. It’s a simple distinction on paper, but in practice, it shapes entire strategies.
Understanding the Roles of Agencies in Clinical Trials
At first glance, it’s abbreviation soup – EMA, FDA, NIHR, OHRP, IRB – but this collection of organizations is responsible for making sure clinical trials are run properly, to protect patients and develop medicines that are safe and effective.
Celebrating 25 Years of Expert Clinical Trial Support
As Siron Clinical turns 25, we look back to where it all started, sail through more than two decades of clinical trial excellence and look forward to what’s next for us and the clients we partner with.
How to Implement a Hybrid FSP/Full-Service Model for Optimal Results
The hybrid FSP/full-service model is gaining traction in clinical research, but what is it and how can you make the most of it? Here we explore what FSP and full-service looks like, how they come together and how you can reap the benefits.
5 Clinical Trial Whitepapers (and Other Things) You Should Read
There is a plethora of information available online about clinical trials, from the basics and fundamentals to glimpses of the future. When you’re overwhelmed by whitepapers, where do you begin? Here are five things we recommend you read – whitepapers, reports, articles and books – to give you new perspectives of the clinical research you work on.
How FSP Models Enhance Drug Development Efficiency
Can the way you engage with a CRO really impact the drug development process? And how can you maximize the positive impact a Functional Service Provider (FSP) agreement can have on your clinical trial efficiency? In this blog post, we look at how the FSP model can help enhance efficiency in clinical research.
4 Reasons Why Choosing a Smaller CRO Can Boost Your Clinical Trial
If you’re looking for the right CRO for your clinical trial, you’re likely considering many factors, including expertise, prior success, budget… but what’s size got to do with it? More than you might think. In this blog post, we look at the benefits of partnering with a smaller CRO.
How small biotech can overcome clinical trial hurdles
Small biotech and biopharma companies are responsible for a significant proportion of newly approved medicines, especially for rare diseases. But with limited resources, budget constraints and a lean structure, they face many challenges with biotech clinical...
How an eTMF can improve your clinical trial
When you’re running a clinical trial, you need to make sure that your records, from protocols to results, are compliant, organized and managed so that they’re always ready for inspection. You can do this by effectively managing your trial master file (TMF) – a crucial element of a successful trial.
Pediatric Rare Disease Clinical Trials
There are many challenges to overcome if pediatric rare disease treatments are being tested, those challenges can be significantly greater.
The Importance of Expertise in Clinical Research FSPs
When a sponsor works with a CRO, they’re looking to bring expertise into their team. But what impact does the type of contract – full-service or FSP – have on this, and how can sponsors get the most out of the CRO’s expertise?
Successful Clinical Operations In Oncology Trials Europe
Cancer is a leading cause of death globally, but the more we understand about this complex group of diseases, the more opportunities we have to target it with new therapies. Running an oncology clinical trial can be challenging; here are three tips to help you succeed.
Orphan Indications: Exploring Siron Clinical’s Specialized Therapeutic Expertise
According to the European Medicines Agency (EMA), about 30 million people in the EU suffer from a rare disease. Since Siron Clinical was founded over 20 years ago, we have been involved in clinical studies with rare diseases.
Effective Communication Strategies with FSP Partners
FSP in clinical research can deliver flexibility and adaptability, helping sponsors keep their clinical trials on track and on budget. To unlock these benefits, effective communication is key. Here Siron Clinical shares some insights to help build a foundation of good communication.
How to Maintain Quality and Compliance with FSPs – 3 Top Tips from Siron Clinical
The increasingly popular Functional Service Provider (FSP) model in clinical research can offer sponsors like biotech and pharma companies flexibility at a lower cost compared to full-service. But what does this mean for compliance? And how can you use FSP to boost quality? We address these questions in this blog post.
Clinical Trial Support – 5 Reasons Why You Don’t Have To Do Everything Yourself
Clinical trials are complex, which means they involve a lot of work and require a range of skills and experience. It can be daunting when you start planning a clinical trial – how will you manage everything that’s needed, especially if you have a small team?
Medical devices in clinical trials can be challenging – here’s what to expect
Medical devices are vital for diagnosing, treating and monitoring diseases, saving lives and keeping us alive. There are about 2 million medical devices on the market today, in more than 7,000 categories. Each of them underwent a journey from innovation through clinical trials to the market. Here we look at medical devices, the challenges you can face with a trial and how to overcome them.
Five Factors to Consider for Your Cardiovascular Clinical Trial
Cardiovascular clinical trials are essential in developing interventions like treatments and medical devices for a wide range of cardiovascular diseases. The sheer size and complexity of cardiovascular clinical trials is just one of the factors that make this...
Clinical Trial Quality Assurance – Why It’s Important and How to Do It
Quality assurance is a critical element of a clinical trial, as it ensures the safety of the participants, as well as the reliability and integrity of the documentation and data, and therefore the validity of your results. But what does it entail, when should it happen, and how can you get it right? We share our insights.
FSP Services for clinical trials – Siron Clinical’s FSP Approach
Siron Clinical’s FSP Approach Partnerships are foundational to clinical research, particularly those between the sponsor, such as a biotech or pharmaceutical company, and the contract research organization (CRO), like Siron Clinical. Clinical research outsourcing has...
Siron Clinical Joins BioFit 2024 to Accelerate Innovation in Clinical Development
We’re excited to announce that we will be heading to Lille, France, for BioFit 2024 on December 3-4, 2024. This premier life sciences event unites leaders from biotech, research, and industry to foster partnerships that accelerate new therapies to market.
3 Ways to Maximize the Benefits of FSP in Biotech
Functional Service Provider (FSP) models can offer biotech and pharma companies more flexibility in the support they get from a CRO while putting them in control. But is it the right choice for your trial? And how can you get the most out of this approach? This blog post explores FSP and its benefits for clinical research.
Experience Matters
As an international contract research organization (CRO), we offer unparalleled knowledge, support, guidance, and experienced clinical research professionals to the biotechnology, life science, and medical device industries. We are committed to leading the development of new and advanced treatments by offering a range of CRO clinical trial services, from Customizable FSP to full-service.