Blogs and News

Discover our latest news and blog articles, dedicated to demystifying drug development, medicine, clinical research, and ethics.

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.

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.

How small biotech can overcome clinical trial hurdles

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 

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.

Effective Communication Strategies with FSP Partners

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.

Medical devices in clinical trials can be challenging – here’s what to expect

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.

3 Ways to Maximize the Benefits of FSP in Biotech

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.

How Artificial Intelligence Can Support Your Clinical Trial

How Artificial Intelligence Can Support Your Clinical Trial

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.

3 Ways to make decentralization support patient centricity

3 Ways to make decentralization support patient centricity

Used in the right way, decentralization can help put patients at the heart of a clinical trial. But if a fully decentralized or hybrid trial is designed and implemented without considering participants’ perspectives, it can result in gaps in data, low participant retention and delays.

Four clinical trial trends to watch in 2023

Four clinical trial trends to watch in 2023

In 2022, the clinical trials industry adjusted to post-pandemic reality, embracing new innovations that emerged from COVID-19. We expect many of these to continue: here we share four trends Siron Clinical will be watching in 2023 and beyond.

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.

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