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Science / Pharmaceutical sciences / Design of experiments / Pharmacology / Clinical research coordinator / Clinical trial / Institutional review board / Good Clinical Practice / Case report form / Clinical research / Research / Pharmaceutical industry


The Study Site Master File and Essential Documents Standard Operating Procedure Office of Health and Medical Research Queensland Health
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Document Date: 2013-10-01 01:47:32


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File Size: 107,98 KB

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City

RGO / /

Company

GCP / /

Country

Australia / /

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Event

FDA Phase / /

Facility

Laboratory Manual Instructions / /

IndustryTerm

Insurance statement / investigational product / investigational products / trial site / blinded investigational product / pharmaceutical products / clinical research site / medicinal products / /

MedicalCondition

injury / /

MedicalTreatment

gene therapy / /

Organization

Research Governance Office / Public Health Organisation / Victorian Managed Insurance Authority / Institutional Review Board / Institution Review Board / Independent Ethics Committee / FDA / Sponsor’s Data Safety Monitoring Committee / Regulatory Authority / Governance Office / Research Ethics and Governance Unit / or Research Governance Office / Study Site Master File and Essential Documents Standard Operating Procedure office of Health / /

Person

Jane Jacobs / Katrina Brosnan Approved / /

Position

Investigator / Author / Governor / Principal Investigator / Coordinator / Director / Applicability Coordinating Principal Investigator / Principal Investigator / research worker / Investigator / where applicable / responsible leader of the team / site Principal Investigator / Document Purpose Investigator / Clinical Trial Coordinator / Institutional Research Governance Officer / District CEO / delegate / investigator and the investigator / correspondence investigator / /

Product

Clinical Drug / /

Technology

gene therapy / /

URL

http /

SocialTag