The Company
clinical trial process expertise – Till Schröer – alias ctpe – is an independent service provider under the leadership of Till Schröer, RN, CCRC dedicated in clinical research process expertise to organize SMO & CRO business, clinical operations, project management, subject & patient recruitment, laboratory logistics and quality and SOP processes.
ctpe clients are primarily pharmaceutical & biotech companies and SMOs & CROs from the USA and Europe. In addition local and central laboratories.
The team is composed of local experts around the world, networked through ctpe. If you need a scientific advice for your program, a medical writer for your report or a complete project management team to run your clinical trial. We will make it happen!
ctpe is located in Münster, close to Osnabrück/Bremen and Dusseldorf and within reach of Frankfurt, Brussels (BEL) and Amsterdam (NL). We offer a broad portfolio of productivity required in the pharmaceutical industry.
The Management
Early in May 2009 Till Schröer founded ctpe and acts as Head of this project in order to use his competence and performance in supporting clinical trials with professional services.
Till has over 20 years of experience in clinical research which he gained at various SMOs / CROs and laboratories in Germany and in the USA, with a specialty expertise in the automated glucose clamp technique running in diabetes trials. He is a registered nurse (RN) from the protestant hospital in Dusseldorf, Germany and a Certified Clinical Research Coordinator (CCRC) from the Association of Clinical Research Professionals in Alexandria, USA.
Till`s sound knowledge in the management of a Clinical Pharmacology Unit (CPU), leading operational teams in the CRO business and his first hand expertise of the needs of the clients further strengthens the expansion and reputation as a service provider for clinical trials.
You can be assured that with Till and his outstanding team, you have experts who will ensure an efficient management of all aspects of your research study.
Areas of Expertise
ctpe offers the services necessary for the successful preparation and performance of your clinical study. Clinical study management is in compliance with the applicable guidelines from EMEA, FDA and GCP/ICH regulations.
Very special expertise is abounded in the therapeutic area of diabetes.
Till has long time know-how in an automated glucose clamp technology, widely accepted as the gold standard for assessing insulin action in vivo. Till self-conducted >500 clamp experiments in Germany and in the USA.
Particular expertise in the following trial designs
- First into man / patients
- Bioequivalence
- Bioavailability
- Single ascending dose
- Multiple ascending dose
- Drug / Drug interaction
- Food effect
- Pharmacodynamic and pharmacokinetic
ctpe’s Company Mission
ctpe’s mission is to be a competent partner, who combines long-standing experience with the professional standards of design, layout and management for clinical studies. Our aim is to provide fast high-quality solutions through maximal support, establishing open communication, creating respectable confidence and transacting smoothly business.
At ctpe, we listen closely to your requirements to deliver first class results. That’s why we’ve structured ctpe to be client-centric in all that we do. Clinical Operations in specific areas is our nucleus and we will manage your processes with clear accountability for overall outcomes and deliverables.