This course outlines the required components of study documentation for all clinical research, defines standard documentation terminology, and applies knowledge of documentation best practices to everyday scenarios faced by study teams. Course Objectives: Outline required components of study documentation for all clinical research Distinguish between documentation regulations and best practice Define standard documentation terminology Apply knowledge of documentation best practices to day-to-day documentation scenarios faced by study team
A best practice is an in-depth study of an organizational practice used in one or more organizations...
Goal: This course has been established to develop an internationally accepted standard of knowledge ...
Study sponsors along with the researchers and the OHRPP share in the responsibilities for protecting...
English: In our Best Practice series we will inform you about examples for good practice and useful...
Clinical study report is one of the main documents during the drug development. The preparation of t...
This Guideline provides guidance on the maintenance of study files, regulatory files and source docu...
Data management is one of the essential areas of responsible conduct of research, as outlined by the...
What is a study protocol? Review the university of Zambia Biomedical Research Ethics Committee Resea...
Developing protocols for clinical research in collaboration with investigators at Boston Children‘s ...
One of the most common inspection findings in investigator site inspections is lack of reliable, acc...
This self-guided course is designed to outline best practices for clinical research. You will gain a...
Documentation is an essential component of good data management and yet data service providers often...
This guideline provides a resource for the development and implementation of research pharmacy proce...
This chapter outlines general guidelines for documentation of clinical occupational therapy services...
The protocol is the central document in a clinical trial. It provides the foundation for other docum...
A best practice is an in-depth study of an organizational practice used in one or more organizations...
Goal: This course has been established to develop an internationally accepted standard of knowledge ...
Study sponsors along with the researchers and the OHRPP share in the responsibilities for protecting...
English: In our Best Practice series we will inform you about examples for good practice and useful...
Clinical study report is one of the main documents during the drug development. The preparation of t...
This Guideline provides guidance on the maintenance of study files, regulatory files and source docu...
Data management is one of the essential areas of responsible conduct of research, as outlined by the...
What is a study protocol? Review the university of Zambia Biomedical Research Ethics Committee Resea...
Developing protocols for clinical research in collaboration with investigators at Boston Children‘s ...
One of the most common inspection findings in investigator site inspections is lack of reliable, acc...
This self-guided course is designed to outline best practices for clinical research. You will gain a...
Documentation is an essential component of good data management and yet data service providers often...
This guideline provides a resource for the development and implementation of research pharmacy proce...
This chapter outlines general guidelines for documentation of clinical occupational therapy services...
The protocol is the central document in a clinical trial. It provides the foundation for other docum...
A best practice is an in-depth study of an organizational practice used in one or more organizations...
Goal: This course has been established to develop an internationally accepted standard of knowledge ...
Study sponsors along with the researchers and the OHRPP share in the responsibilities for protecting...