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Researcher-oriented clinical trials

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If you wish to participate in the K-master project, the procedures will not deviate from those already in place for standard investigator-initiated trial (IITs).

Researcher-oriented clinical trials
1
arrow Clinical Trial Registration

dot When new clinical trials are initiated, KCSG will recruit research institutions through
each division.

dot If you wish to participate, you will be subject to the same registration procedure as
standard IITs.

1
bar
arrow Clinical Trial Support System

dot The K-master project will support you throughout the whole clinical trial period.

dot With the support of a dual contract research organization (CRO), you can be involved
in protocol development, clinical trial registration and monitoring.

dot The K-MASTER project consults directly with pharmaceutical companies so that
efficient clinical trials can be conducted.

Clinical Trial Support System
3
bar
arrowClinical Trial Planning

The K-master project supports researchers to propose and carry out necessary clinical trials.

※ To plan a clinical trial

dot The study plan can be submitted to the KCSG and the K-master project coordinators.
(see our website for more information)

dot Once the synopsis has been approved by the Clinical Trial Steering Committee,
the protocol is developed by the CRO and approved by the K-master project;
the drug is then obtained from the Clinical Trial Committee.

dot We will also provide research monitoring and quality control for subsequent clinical
trials, as well as results analysis and reporting.

Clinical Trial Planning
연구자 중심 임상시험
1
arrow Clinical Trial Registration

dot When new clinical trials are initiated, KCSG will recruit research institutions
through each division.

dot If you wish to participate, you will be subject to the same registration
procedure as standard IITs.

1
bar
arrow Clinical Trial Support System

dot The K-master project will support you throughout the whole clinical trial
period.

dot With the support of a dual contract research organization (CRO), you can be
involved in protocol development, clinical trial registration and monitoring.

dot The K-MASTER project consults directly with pharmaceutical companies
so that efficient clinical trials can be conducted.

Clinical Trial Support System
3
bar
arrowClinical Trial Planning

The K-master project supports researchers to propose and carry out necessary clinical trials.

※ To plan a clinical trial

dot The study plan can be submitted to the KCSG and the K-master project
coordinators. (see our website for more information)

dot Once the synopsis has been approved by the Clinical Trial Steering
Committee, the protocol is developed by the CRO and approved by
the K-master project; the drug is then obtained from the Clinical Trial
Committee.

dot We will also provide research monitoring and quality control for
subsequent clinical trials, as well as results analysis and reporting.

Clinical Trial Planning
Researcher-oriented clinical trials
1
arrow Clinical Trial Registration

dot When new clinical trials are initiated, KCSG will recruit research institutions
through each division.

dot If you wish to participate, you will be subject to the same registration
procedure as standard IITs.

1
bar
arrow Clinical Trial Support System

dot The K-master project will support you throughout the whole clinical trial
period.

dot With the support of a dual contract research organization (CRO), you can be
involved in protocol development, clinical trial registration and monitoring.

dot The K-MASTER project consults directly with pharmaceutical companies
so that efficient clinical trials can be conducted.

Clinical Trial Support System
3
bar
arrowClinical Trial Planning

The K-master project supports researchers to propose and carry out necessary clinical trials.

※ To plan a clinical trial

dot The study plan can be submitted to the KCSG and the K-master project
coordinators. (see our website for more information)

dot Once the synopsis has been approved by the Clinical Trial Steering
Committee, the protocol is developed by the CRO and approved by the
K-master project; the drug is then obtained from the Clinical Trial
Committee.

dot We will also provide research monitoring and quality control for sub-
sequent clinical trials, as well as results analysis and reporting.

Clinical Trial Planning
Researcher-oriented clinical trials
arrow Clinical Trial Registration

dot When new clinical trials are initiated, KCSG will recruit research institutions through each division.

dot If you wish to participate, you will be subject to the same registration procedure as standard IITs.

arrow Clinical Trial Support System

dot The K-master project will support you throughout the whole clinical trial period.

dot With the support of a dual contract research organization (CRO), you can be involved in protocol

Clinical Trial Support System
arrow Clinical Trial Planning

The K-master project supports researchers to propose and carry out necessary clinical trials.

※ To plan a clinical trial

dot The study plan can be submitted to the KCSG and the K-master project coordinators. (see our website for more information)

dot Once the synopsis has been approved by the Clinical Trial Steering Committee, the protocol is developed by the CRO and approved by the K-master project; the drug is then obtained from the Clinical Trial Committee.

dot We will also provide research monitoring and quality control for subsequent clinical trials, as well as results analysis and reporting.

Clinical Trial Planning