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Our common goal in clinical research is the protection and safeguard of trial subjects’ rights, safety and well-being. Benefit from Accovion’s expertise in protocol design, patient information and informed consent processes that promote fast reviews by ethical and regulatory bodies.
We provide guidance on:
- Social value - the research must be worth doing
- Scientific merit - the design and methods must be scientifically sound
- Respect for persons - implies concern for the safety, well-being, beliefs and customs of individuals and communities taking part in research
- Respect for vulnerable persons - researchers must be especially sensitive toward persons whose autonomy is in some way compromised
- Privacy and confidentiality - protect patients from harm that might result from access to personal and sensitive information
- Fair subject and community selection - the benefits and burdens of research must be shared fairly among individuals and communities
- Favorable balance of benefits and harms - because of the purpose of the research
- Collaborative partnerships - to ensure that research is relevant and acceptable
- Ethical review - no research involving humans can begin until the ethics committee has granted approval
- Professional competence - researchers must be technically competent in their specific fields to conduct a study
Dr. Rainer Porrmann
Manager Study Coordination & Clinical Trial Submission
+49 6196 7709-385
