Advance Course in Clinical Research (Audio+Test+Certificate)

What you’ll learn

• Importance & Types of Clinical Research
• ICH GCP Principles
• Essential Documents [For Example- Protocol, Informed Consent Form (ICF), Case Report Form (CRF), & Investigators Brochure (IB)]
• Regulatory Authorities or Central Licensing Authorities
• Audit & Inspection
• Special Population Clinical Trials [For Example- Geriatric, Paediatric & Special & Vulnerable Population]
• Clinical Trial Designs
• Case Studies
• Clinical Trial Terminologies
• Clinical Research Phases & Key Players

Requirements

• Graduate or postgraduate degree in Pharmacy
• Graduate or postgraduate degree in Medicine or any healthcare stream
• Graduate or postgraduate degree in Life Sciences
• Anyone from or related to healthcare, pharma, biotech and clinical research industry

Description

The objective of the Advance Course in Clinical Research is to provide detailed clinical research knowledge to students, Investigators, Study Coordinators, Sponsors, Clinical Project Managers, Monitors, and any other Clinical Study staff to reach top-end positions in the clinical research Industry.

This course is developed and structured in a manner considering the advance level of knowledge required in view of industry expectations. This course is integrated with practice tests in between including case study-based scenarios. In this course, you’ll learn principles and processes of clinical research, essential documents, clinical trial terminologies, understanding of the design & types of clinical trials in developing new treatments and interventions.

Who Should Enroll?

1. Graduate or postgraduate degree in Pharmacy
2. Graduate or postgraduate degree in Medicine or any healthcare stream
3. Graduate or postgraduate degree in Life Sciences
4. Anyone from a related healthcare industry

What This Course Covers?

• Module 1: Importance & Types of Clinical Trials
• Module 2: Clinical Trial Phases & Key Players at Glance
• Module 3: ICH GCP Principles
• Module 4: Essential Documents

– Protocol

– Informed Consent Document (ICD)

– Case Report Form (CRF)

– Investigators Brochure (IB)

• Module 5: Clinical Trial Regulatory Bodies

– US-FDA

– MHRA

– EMA

– PMDA

– CDSCO

• Module 6: Audit & Inspection
• Module 7: Special Population Clinical Trials

– Geriatric

– Paediatric

– Special & Vulnerable Population etc.

• Module 8: Clinical Trial Designs
• Module 9: Case Studies
• Module 10: Clinical Trial Terminologies

Who this course is for:

• Suited for people interested to learn about advance clinical research.
• Suited for CROs, Pharma, Hospitals, Ethics Committees, Corporate Training.
• Suited for clinical trial professionals for refresher training.
• Suited for people aspiring to start career in clinical research.