From Idea to Implementation
Whether as permanent support or selectively on a specific topic: I am happy to share my knowledge with you. Let us start with a cost-free 1,5 hour online-meeting, to identify your needs and to get to know each-other. If the chemistry is right and my experience matches your needs, I will be happy to provide you with a quote for further support.
You are a physician in a private practice or working in a hospital? You do have the impression, that performing clinical studies might be beneficial to both your patients and your income? You might even have performed one or two studies in the past, but you do not know how and where to start to do so on a regular basis?
I am happy to discuss the „must-have´s“ and „nice-to-have´s“ to support your start. We might
Feel free to get in touch!
You are performing clinical studies for many years and do have quite an extensive experience? You would like to grow this part of your business but due to time constraints it is difficult to manage? Potential business partners asked for Standard Operating Procedures or higher recruitment rates, but you never find the time to tackle these tasks?
Get in touch with me! I am happy to take over some of those tasks, keeping your back free from administrative overload.
During the more than 20 years that I have been conducting clinical trials at emovis, my knowledge and experience of recruitment activities has constantly expanded. During this time, we have tried out countless activities, statistically recorded the outcome, evaluated the results and constantly optimised our recruitment activities over the years.
I am happy to share this experience with you. Whether you want to establish a system for identifying suitable study participants in your practice for all studies conducted at your site or would like to recruit additional participants beyond the practice's patient pool.
I have extensive knowledge of the resources you need to deploy to maximise your recruitment success. Let me help you implement this on your site.
Link zum Training Recruitment Campaigns
Are you aware, that Standard Operating Procedures (SOPs) are requested for sites more and more and might become compulsory for sites during the upcoming years?
Quality Management Systems for clinical studies are different to those you will have established already in your practice or hospital. You might use your already existing SOPs as basis, but you will need to add additional ones to cover the needs for clinical research.
During my time as CEO of emovis, I wrote several versions of our SOPs on my own. This enabled me to learn from scratch which SOPs are more of a hindrance in practice, and which are helpful. I am looking forward to sharing my experiences with you, having always in my mind of providing high quality data without making day-to-day life for you and your staff extremely annoying.
Eventuell hier ein pdf zum Download mit einer Beispiel-SOP einfügen.
Link zum Training Quality Management
