Search by property

This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Agreement  + (GLOSSARY - Agreement)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Audit  + (GLOSSARY - Audit)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Blinding/Masking  + (GLOSSARY - Blinding/Masking)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Case Report Form (CRF)  + (GLOSSARY - Case Report Form (CRF))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Certified Copy  + (GLOSSARY - Certified Copy)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial  + (GLOSSARY - Clinical Trial)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Clinical Trial/Study Report (CSR)  + (GLOSSARY - Clinical Trial/Study Report (CSR))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Comparator  + (GLOSSARY - Comparator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Compliance (in relation to trials)  + (GLOSSARY - Compliance (in relation to trials))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Computerised Systems Validation  + (GLOSSARY - Computerised Systems Validation)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Contract Research Organisation (CRO)  + (GLOSSARY - Contract Research Organisation (CRO))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Data Acquisition Tool (DAT)  + (GLOSSARY - Data Acquisition Tool (DAT))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Data Integrity  + (GLOSSARY - Data Integrity)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Independent Data Monitoring Committee (IDMC)  + (GLOSSARY - Independent Data Monitoring Committee (IDMC))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Informed Consent  + (GLOSSARY - Informed Consent)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Inspection  + (GLOSSARY - Inspection)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC)  + (GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Interim Clinical Trial/Study Report  + (GLOSSARY - Interim Clinical Trial/Study Report)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigational Product  + (GLOSSARY - Investigational Product)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator  + (GLOSSARY - Investigator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Investigator’s Brochure (IB)  + (GLOSSARY - Investigator’s Brochure (IB))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Metadata  + (GLOSSARY - Metadata)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Protocol Amendment  + (GLOSSARY - Protocol Amendment)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Randomisation  + (GLOSSARY - Randomisation)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Regulatory Authorities  + (GLOSSARY - Regulatory Authorities)

• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Serious Adverse Event (SAE)  + (GLOSSARY - Serious Adverse Event (SAE))

• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Service Provider  + (GLOSSARY - Service Provider)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Signature  + (GLOSSARY - Signature)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Source Records  + (GLOSSARY - Source Records)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor  + (GLOSSARY - Sponsor)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor-Investigator  + (GLOSSARY - Sponsor-Investigator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sub-Investigator  + (GLOSSARY - Sub-Investigator)
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Suspected Unexpected Serious Adverse Reaction (SUSAR)  + (GLOSSARY - Suspected Unexpected Serious Adverse Reaction (SUSAR))
• Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Vulnerable Participants  + (GLOSSARY - Vulnerable Participants)
• Reference:USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 GLOSSARY OF TERMS  + (GLOSSARY OF TERMS)
• Reference:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016 GUIDELINE 18  + (GUIDELINE 18)
• Reference:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016 GUIDELINE 19  + (GUIDELINE 19)
• Reference:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 Glossary  + (Glossary)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - 1.5 Regulatory requirements  + (Glossary - 1.5 Regulatory requirements)
• Reference:ICH ICH E9 Guideline 1998 Glossary - Double-Dummy  + (Glossary - Double-Dummy)
• Reference:ICH ICH E9 Guideline 1998 Glossary - Dropout  + (Glossary - Dropout)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - Good Clinical Practice (GCP)  + (Glossary - Good Clinical Practice (GCP))
• Reference:ICH ICH E9 Guideline 1998 Glossary - IDMC  + (Glossary - IDMC)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - adverse event  + (Glossary - adverse event)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - adverse reaction  + (Glossary - adverse reaction)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - audit of a trial  + (Glossary - audit of a trial)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - case -report form (CRF)  + (Glossary - case -report form (CRF))
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial  + (Glossary - clinical trial)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - clinical trial Phases  + (Glossary - clinical trial Phases)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - comparator product  + (Glossary - comparator product)
• Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract  + (Glossary - contract)