Clinical Monitoring
Clinical Monitors, also referred to as Clinical Research Associates (CRAs), guarantee the correct and complete conduct of the clinical study. Our monitors help to ensure that trials are conducted efficiently in accordance with the protocol and in compliance with SOPs, GCP and applicable regulatory requirements. The key task in monitoring is control and supervision of conduction / implementation of clinical studies in accordance with the “Good Clinical Practice (GCP)”, the Declaration of Helsinki and the corresponding laws and regulations (pharmaceutical law, Medical Devices Law, etc.) of the individual countries performing clinical trials.
We help you conserve your valuable resources and reduce costs.
Strengths
- flexible and highly motivated staff
- deep experience in a wide range of indications
- international capabilities
In the following you will find our national and international capabilities.
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Dr. Notghi Contract Research GmbH offers you a complete service range in clinical monitoring for full service and partial service solutions.
Services at a glance
- Monitoring in accordance with protocol and regulatory requirements
- CRF (Case Report Form) completion
- Drug accountability
- On- and off-site monitoring
Our experts will gladly provide you with personal consultation. We look forward to hearing from you! Contact