Diploma in Clinical Research, Pharmacovigilance and medical writing

QREC Clinical Research Institute
Distance

Rs 14,999
You can also call the Study Centre
75973... More
Compare this course with other similar courses
See all

Important information

  • Diploma
  • Distance learning
  • Duration:
    6 Months
  • When:
    Flexible
  • Online campus
  • Delivery of study materials
  • Support service
  • Personal tutor
  • Examinations- physical attendance required
Description

Diploma in clinical research will provide you with an in-depth understanding of the core areas of the clinical research and enhance your skills and knowledge to the level expected of a Clinical Research Associate / Professional.
In this Diploma we are providing you knowledge about Clinical Research, Pharmacovigilance and medical writing.
This Diploma course is 6 month program initiating with online teaching and enhance skills of Students and Professionals.

Important information
Venues

Where and when

Starts Location Timetable
Flexible
Distance learning

Frequent Asked Questions

· What are the objectives of this course?

our success lies in the success of our students .We make every effort to equip and prepare our students to undertake successful career.

What you'll learn on the course

To gain knowledge about Clinical trial procedures
Learn about quality management
To convert your Clinical practice into academic research for pub
To enrich knowledge on Clinical research & procedures

Teachers and trainers (5)

Dr. Deepak langade
Dr. Deepak langade
Biostats and Clinical Data Management

Medha saharasbudhe
Medha saharasbudhe
Faculty

Mrs. Neha Ghondhale
Mrs. Neha Ghondhale
Regulatory affairs

neelam jhangiani
neelam jhangiani
Faculty

Ritesh khandelwal
Ritesh khandelwal
Clinical operations and regulatory affairs

Course programme

Course curriculum for Diploma in Clinical Research- Module.1- General Introduction to Clinical Research Module.2 – Clinical Pharmacology Module.3- Drug Discovery, Development & Phases of Clinical Trial Module.4- Credentials of Clinical Trial Module.5- CT Activities – Before, During & After Module.6- Roles & Responsibilities of Clinical Research Professional Module.7- Need of Ethics in Clinical Research Module.8- An Introduction to Clinical Data Management Module.9- Regulatory Affairs – Indian & Other countries requirements
Course curriculum for PvG and MW Module-10. General introduction to PvG Module-11. Basic principles of pharmacovigiliance Module-12. Scope of pharmacovigiliance Module-13. Regulatory Guidelines & Laws in Pharmacovigiliance Module- 14. Medical Writing

Compare this course with other similar courses
See all