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Virtual visits: moving clinical trials visits from clinics to homes -  ScienceDirect
Virtual visits: moving clinical trials visits from clinics to homes - ScienceDirect

Schedule of Events. Example visit and assessment specification from a... |  Download Scientific Diagram
Schedule of Events. Example visit and assessment specification from a... | Download Scientific Diagram

Free Clinical Trial Templates | Smartsheet
Free Clinical Trial Templates | Smartsheet

Therapeutics for Dengue: Recommendations for Design and Conduct of  Early-Phase Clinical Trials | PLOS Neglected Tropical Diseases
Therapeutics for Dengue: Recommendations for Design and Conduct of Early-Phase Clinical Trials | PLOS Neglected Tropical Diseases

On Biostatistics and Clinical Trials: Study Day in Clinical Study Protocol
On Biostatistics and Clinical Trials: Study Day in Clinical Study Protocol

Consent - Health Literacy in Clinical Research
Consent - Health Literacy in Clinical Research

PLOS Medicine: Assessment of Adverse Events in Protocols, Clinical Study  Reports, and Published Papers of Trials of Orlistat: A Document Analysis
PLOS Medicine: Assessment of Adverse Events in Protocols, Clinical Study Reports, and Published Papers of Trials of Orlistat: A Document Analysis

Clinical Trials: Coordinating Schedules – InterSECT Job Simulations
Clinical Trials: Coordinating Schedules – InterSECT Job Simulations

On Biostatistics and Clinical Trials: Study Day in Clinical Study Protocol
On Biostatistics and Clinical Trials: Study Day in Clinical Study Protocol

Clinical Trials Adverse Event Reporting Guide, 2020 Edition | CenterWatch
Clinical Trials Adverse Event Reporting Guide, 2020 Edition | CenterWatch

Clinical Trials Europe 2020 | 11/02/20-12/04/19 | mdgroup
Clinical Trials Europe 2020 | 11/02/20-12/04/19 | mdgroup

Budget and Billing Workbook | Research Management Group (RMG) | Stanford  Medicine
Budget and Billing Workbook | Research Management Group (RMG) | Stanford Medicine

Table 2 from Guidelines for time-to-event end point definitions in breast  cancer trials: results of the DATECAN initiative (Definition for the  Assessment of Time-to-event Endpoints in CANcer trials)†. | Semantic Scholar
Table 2 from Guidelines for time-to-event end point definitions in breast cancer trials: results of the DATECAN initiative (Definition for the Assessment of Time-to-event Endpoints in CANcer trials)†. | Semantic Scholar

Clinical trial regimen: Schedule of events. | Download Scientific Diagram
Clinical trial regimen: Schedule of events. | Download Scientific Diagram

Figure 1 from Knowledge-data integration for temporal reasoning in a clinical  trial system | Semantic Scholar
Figure 1 from Knowledge-data integration for temporal reasoning in a clinical trial system | Semantic Scholar

Is Retraining on Good Clinical Practice Guidelines Effective?
Is Retraining on Good Clinical Practice Guidelines Effective?

Traumatic injury clinical trial evaluating tranexamic acid in children  (TIC-TOC): study protocol for a pilot randomized controlled trial | Trials  | Full Text
Traumatic injury clinical trial evaluating tranexamic acid in children (TIC-TOC): study protocol for a pilot randomized controlled trial | Trials | Full Text

An analysis of subject recruitment issues for an HCV investigational drug  clinical trial | Semantic Scholar
An analysis of subject recruitment issues for an HCV investigational drug clinical trial | Semantic Scholar

Schedule of events for PReDICT study. NOTE: Remitters to the acute... |  Download Scientific Diagram
Schedule of events for PReDICT study. NOTE: Remitters to the acute... | Download Scientific Diagram

Clinical Trials: Coordinating Schedules – InterSECT Job Simulations
Clinical Trials: Coordinating Schedules – InterSECT Job Simulations

Writing a Protocol | CHOP Institutional Review Board
Writing a Protocol | CHOP Institutional Review Board

Participant timeline – GUIDANCE FOR CLINICAL TRIAL PROTOCOLS
Participant timeline – GUIDANCE FOR CLINICAL TRIAL PROTOCOLS

The CRC's Guide to Coordinating Clinical Research | CenterWatch
The CRC's Guide to Coordinating Clinical Research | CenterWatch