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

PDF) A double-blind, randomised, vehicle-controlled clinical study to  evaluate the efficacy of MAS065D in limiting the effects of radiation on  the skin: Interim analysis
PDF) A double-blind, randomised, vehicle-controlled clinical study to evaluate the efficacy of MAS065D in limiting the effects of radiation on the skin: Interim analysis

Clinical Trial Services
Clinical Trial Services

FAQ | Pharma Instinct
FAQ | Pharma Instinct

Immunogenicity and safety of a third dose of CoronaVac, and immune  persistence of a two-dose schedule, in healthy adults: interim results from  two single-centre, double-blind, randomised, placebo-controlled phase 2 clinical  trials -
Immunogenicity and safety of a third dose of CoronaVac, and immune persistence of a two-dose schedule, in healthy adults: interim results from two single-centre, double-blind, randomised, placebo-controlled phase 2 clinical trials -

Assessing the value of interim analyses in clinical trials - PMLiVE
Assessing the value of interim analyses in clinical trials - PMLiVE

Challenging Issues in Clinical Trial Design: Part 4 of a 4-Part Series on  Statistics for Clinical Trials - ScienceDirect
Challenging Issues in Clinical Trial Design: Part 4 of a 4-Part Series on Statistics for Clinical Trials - ScienceDirect

CLINICAL STUDY REPORTING - Assessing the Value of Interim Analyses in Clinical  Trials
CLINICAL STUDY REPORTING - Assessing the Value of Interim Analyses in Clinical Trials

American Society of Clinical Oncology Road to Recovery Report: Learning  From the COVID-19 Experience to Improve Clinical Research and Cancer Care |  Journal of Clinical Oncology
American Society of Clinical Oncology Road to Recovery Report: Learning From the COVID-19 Experience to Improve Clinical Research and Cancer Care | Journal of Clinical Oncology

A Guide to Phase 1 Clinical Trial Designs
A Guide to Phase 1 Clinical Trial Designs

Mortality outcomes with hydroxychloroquine and chloroquine in COVID-19 from  an international collaborative meta-analysis of randomized trials | Nature  Communications
Mortality outcomes with hydroxychloroquine and chloroquine in COVID-19 from an international collaborative meta-analysis of randomized trials | Nature Communications

The use of interim data and Data Monitoring Committee recommendations in  randomized controlled trial reports: frequency, implications and potential  sources of bias | BMC Medical Research Methodology | Full Text
The use of interim data and Data Monitoring Committee recommendations in randomized controlled trial reports: frequency, implications and potential sources of bias | BMC Medical Research Methodology | Full Text

Assessing the value of interim analyses in clinical trials - PMLiVE
Assessing the value of interim analyses in clinical trials - PMLiVE

SURPASS Study Confirms Real-World Safety and Efficacy of Watchman FLX  Through 45 Days – Consult QD
SURPASS Study Confirms Real-World Safety and Efficacy of Watchman FLX Through 45 Days – Consult QD

Sugemalimab versus placebo, in combination with platinum-based  chemotherapy, as first-line treatment of metastatic non-small-cell lung  cancer (GEMSTONE-302): interim and final analyses of a double-blind,  randomised, phase 3 clinical trial - The Lancet
Sugemalimab versus placebo, in combination with platinum-based chemotherapy, as first-line treatment of metastatic non-small-cell lung cancer (GEMSTONE-302): interim and final analyses of a double-blind, randomised, phase 3 clinical trial - The Lancet

UCD Clinical Research Centre Annual Report by Advantage Point - Issuu
UCD Clinical Research Centre Annual Report by Advantage Point - Issuu

Randomised clinical trials in critical care: past, present and future |  SpringerLink
Randomised clinical trials in critical care: past, present and future | SpringerLink

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

Efficacy, safety, and lot-to-lot immunogenicity of an inactivated  SARS-CoV-2 vaccine (BBV152): interim results of a randomised, double-blind,  controlled, phase 3 trial - The Lancet
Efficacy, safety, and lot-to-lot immunogenicity of an inactivated SARS-CoV-2 vaccine (BBV152): interim results of a randomised, double-blind, controlled, phase 3 trial - The Lancet

Adaptive designs in clinical trials: why use them, and how to run and report  them | BMC Medicine | Full Text
Adaptive designs in clinical trials: why use them, and how to run and report them | BMC Medicine | Full Text

Monitoring Report Template Clinical Trials (1) - TEMPLATES EXAMPLE |  TEMPLATES EXAMPLE | Clinical trials, Report template, Clinic
Monitoring Report Template Clinical Trials (1) - TEMPLATES EXAMPLE | TEMPLATES EXAMPLE | Clinical trials, Report template, Clinic

How to develop a Statistical Analysis Plan (SAP) for Clinical Trials
How to develop a Statistical Analysis Plan (SAP) for Clinical Trials

Unlocking Clinical Trial Data to Uncover New Therapeutic Opportunities –  Drug Discovery World (DDW)
Unlocking Clinical Trial Data to Uncover New Therapeutic Opportunities – Drug Discovery World (DDW)