Incoming and outgoing links Clinical trial
Back to articleOutgoing links
- Adverse event
- Adverse event
- Amendment
- Benefit - risk - analysis
- Bias
- Case number calculation in clinical studies
- Case report form
- Certifications in clinical research
- Clinical investigator
- Clinical research associate
- Clinical research organization
- Clinical study report
- Clinical trial
- Clinical trial
- Clinical trial manager
- Consort statement
- Contract research organisation
- Declaration of consent
- Declaration of helsinki
- Dimdi
- Dossier on the investigational medicinal product
- Electronic case report form
- Endpoint
- Ethics committee
- Eudract
- Evidence level
- Fda
- Feasibility study
- Feasibility study
- Final report
- Freiburg international ethics committee
- German register of clinical studies
- Good clinical practice
- Higher federal authorities
- Impd
- Informed consent form
- International conference on harmonisation
- Investigational product
- Investigator
- Investigator initiated trial
- Investigator meeting
- Iso 14155
- Jadad scale
- Jadad score
- Medical devices act
- Non-interventional study
- Notified body
- Notified body
- Openclinica
- Patient consent form
- Pharmacovigilance
- Project management
- Quality assurance
- Query
- Randomization
- Remuneration of investigators
- Risk - benefit - analysis
- Robert koch institute
- Secutrial®
- Serious adverse event
- Sponsor
- Standard operating procedure
- Strobe
- Study nurse
- Subjects in need of protection
- Test person
- Trial master file
- World health organization
- Xclinical