PCR Course Overview
Proper Conduct of Research (PCR) Course
The Proper Conduct of Research (PCR) Standard Operating
Procedures, known as the PCR-SOPs, are a set of guidelines developed by
the NHG Group Research & Innovation to provide detailed procedures
on conducting research in accordance with applicable guidelines and regulations.
The Proper Conduct of Research (PCR) Course seeks to equip
Clinical Research professionals with the knowledge and skills in the proper
conduct of research.
The entire PCR Course comprises 4 main modules, with multiple topics covered
under each module. Participants are encouraged to sign up for all 4 modules
to obtain a holistic appreciation of all the aspects of PCR. There are
no pre-requisites to be fulfilled for taking each PCR Modules.
Course Features
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Contents updated with the latest regulatory controls, guidelines and SOPs
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Online Learning format for greater flexibility and accessibility
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Interactive lectures and quizzes to enhance learning and understanding
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Case studies for selected topics to deepen learning, understanding and knowledge application
Who Should Attend
This course is intended for Investigators, Researchers, Clinical Research Coordinators and Research Assistants.
PCR Modules
See the synopsis for each PCR Module below:
PCR-001: Subject Recruitment and Informed Consent
In this online module, Participants will gain knowledge and application principles for research subject recruitment and informed consent based on ethical and regulatory requirements throughout the phase of planning, designing, conducting and maintaining proper documentation. Best practices, tips and common errors will also be covered in this course which includes interactive case scenarios, and quizzes and informative reference materials.
PCR-002: Study Start-Up, Data Management, Investigational Product & Safety Reporting
In this online module, Participants will gain knowledge and principles for Study Start-Up, Research Data Management, and the types of essential documents to be maintained in the investigator file. Participants will also gain a better understanding about the safety reporting requirements for both investigator-initiated and sponsored trials, and an appreciation of the myriad of regulations governing investigational product management in clinical trials. Participants will learn about handling investigational products in accordance with Good Clinical Practice principles.
PCR-003: Research Data Collection & Budgeting
In this online module, participants will learn about the general principles involved in budgeting, design and use of a case report form, database design and have an overview understanding of how REDCap is used in NHG to aid in data analysis and capture in research.
conduct of research studies.
PCR-400: Monitoring, Audits and Inspections
This online course features the closely related topics of monitoring, audits and inspections. The content will allow participants to understand the purpose of site monitoring, responsibilities of monitors, and concepts surrounding risk-based monitoring; including the process of audits and inspections, conducted either by external parties and/or regulatory authorities.
Schedule
This Online PCR Course is available on a continuous basis (via E-Learning).
Registration
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Registration for this Course is currently open. Go to the PCR Course Registration (via FormSG) here.
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For NHG Staff: Register here for the PCR course. Download the NHG Staff Self-Registration Guide for PCR Course here.
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See the Course Registration FAQs here.
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See how to Download your Course E-Certificate here.
Contact information
For any enquiries, please contact the Research Course Admin at research_courseadmin@nhg.com.sg
Note/Disclaimer: Participants are encouraged to select the courses based on their learning needs. All courses are available to the public. Please note that course details are subjected to changes without prior notice. Please check the respective course registration page for more information.