Showing below up to 50 results in range #1 to #50.
- ADR → Adverse drug reaction
- AE → Adverse event
- AI → Artificial intelligence
- ALCOA+CCEA → ALCOA
- ALCOA-C Principles → ALCOA
- Adverse Drug Reaction → Adverse drug reaction
- Adverse Event → Adverse event
- Artificial Intelligence → Artificial intelligence
- BIMO → FDA Bioresearch monitoring
- CA → Regulatory authority
- CAPA → Corrective and Preventive Action
- CRO → Contract Research Organization
- CTIS → Clinical Trials Information System
- Case Report Form → Case report form
- Clinical Trial Phases → Phases of clinical trials
- Clinical Trials Regulation (EU) No 536/2014 → Regulation (EU) No 536/2014
- Clinical trial (study) → Clinical study
- Corrective and Preventive Actions → Corrective and Preventive Action
- DSMB → Independent data-monitoring committee
- Data and Safety Monitoring → Data and safety monitoring
- EC → Ethics committee
- Essential Documents → Essential documents
- European Union Clinical Trials Regulation → Clinical Trials Regulation (EU) No 536/2014
- GCP → Good Clinical Practice
- Good clinical practice → Good Clinical Practice
- IB → Investigator's brochure
- ICH → The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use
- IMP → Investigational product
- IRB → Institutional review board
- Independent Data-Monitoring Committee → Independent data-monitoring committee
- Independent Ethics Committee → Independent ethics committee
- Index → Codex of clinical research
- Inspection → Regulatory inspection
- Institutional Review Board (IRB) → Institutional review board
- Investigator's Brochure → Investigator's brochure
- Investigator’s Brochure → Investigator's brochure
- LAR → Legally acceptable representative
- Main Page → Codex of clinical research
- Phase II Clinical Trials → Phase II clinical trials
- Phase I Clinical Trials → Phase I clinical trials
- Phases of Clinical Trials → Phases of clinical trials
- RA → Regulatory authority
- Regulatory agency → Regulatory authority
- Regulatory approval → Regulatory authority#Regulatory approval
- Regulatory submissions → Regulatory authority#Regulatory submission
- Researcher → Investigator
- SAE → Serious adverse event (serious adverse drug reaction)
- SI → Sub-investigator
- SOP → Standard operating procedures
- Subinvestigator → Sub-investigator