If you’re looking for the right CRO to support your clinical trial operations, 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...
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...
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...
There are many challenges to overcome when running a clinical trial, and if treatments for pediatric rare diseases are being tested, those challenges can be significantly greater. Siron Clinical has expertise in these crossover therapeutic areas – here’s how we...
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? For a small biotech or pharma company, a...
Cancer is a leading cause of morbidity and mortality 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...
