Every clinical trial is made up of multiple moving parts and everyone needs to work smoothly and consistently to deliver projects on time and meet expectations, i.e. deliver reliable study data and at the same time to protect study participants.

If a part within this machine (i.e. clinical study) breaks down, a ripple effect occurs across the entire organization, resulting in project delays and huge cost overruns but what even more important may put study participants at risk and negatively affect quality of data.

So how can we turn clinical trials into a well-oiled machine? How can we systemize your processes and ensure more consistent results?

The answer is with… standard operating procedures (SOPs) — a way to document the processes from start to finish.

During this training you will learn how to plan and prepare effective SOPs that will help in quality maintenance if improvement and work efficiency.

The training is dedicated to staff from the investigational sites, CROs, pharma or biotech companies or vendors who have already experience in clinical trials conduct and might be the process owners or might be delegated for SOP writing.