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Clinical Data Management

Basics of case report form

"Case report form (CRF) is designed to collect the patient data in a clinical trial as per the clinical trial protocol"

How to resolve reference ranges issue in RAVE eDC- CRA, CRC and DM prospective.

Whether you are a Clinical Research Associate (CRA), Clinical Research Coordinator (CRC) or a Clinical Data Manager (CDM), you all face...

What is the difference between the Central lab and local lab in clinical research?

Before understanding the difference between central lab and local lab, let's understand about "why lab tests are conducted"

Parts of a clinical trial protocol and Clinical Data Management (CDM) prospective to review

This blog talks about Protocol parts and key information needed for any Data Manager to design CRF. Protocols are quite specific to...

When to Start and Stop collecting Adverse Events

When to start and when to stop? Before answering this question, let’s understand where the confusion relies. Generally we...

ECOG Performance Status

ECOG Performance Status-scale was developed by Eastern Cooperative Oncology Group. Now this group is a part of ECOG-ACRIN Cancer Research Group.This scale...

Important data points in Protocol for CRFs Creation (CDM Prospective):

Reading of whole protocol is quite important and indispensable act but by keeping following points in mind, one can read protocol with...

Parts of a clinical trial protocol and Clinical Data Management (CDM) prospective to review

This blog talks about Protocol parts and key information needed for any Data Manager to design CRF. Protocols are quite specific to studies but...

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