Clinical data mgmt

Duration

Five days of classroom sessions followed by an evaluation test

Topics Covered

  • Overview of New Drug Development
  • Introduction to Clinical Research
  • GCP and Schedule Y
  • 21 CFR Part 11
  • Regulations and Ethics
  • Informed Consent Process
  • Clinical Trial Phases
  • Clinical Trial Design
  • Clinical Trial Protocol
  • Study Conduct
  • Essential Documents

Eligibility

No specific pre-requisite.

Data mgmt small

Who should Attend?

  • SAS® Programmers / Statisticians working in Clinical Domain
  • Candidates who have begun a career in Clinical Trial Data Analytics or Clinical Research
  • Candidates trained in SAS® and aspiring to enter the Clinical Trial Services Industry
  • Candidates who are required to learn about the Clinical Trial Domain as part of their profession or academic studies

Tools Used

Not Applicable

Batch Size

10-15 students per batch

Features of the Course

This 5-day training program aims to equip the participants with basic knowledge about the Clinical Trials Domain. Participants get exposure to a variety of topics ranging from an overview of drug development to essential documentation for Clinical Trials, thereby getting ready to work on projects with confidence.

  • The training course consists of videos on individual topics with an approximate run time ranging between 30 and 90 minutes each.
  • Training is delivered by an eminent faculty in the industry – Dr. Ravindra Ghooi, using relevant examples from his rich academic and professional experience
  • The batches can be planned as per your convenience
  • The faculty is available to address the questions of the participants in the middle of the course and at the end of the course
  • Payment can be done by Cheque/DD/Credit Card/Debit card
  • Group Discounts / Corporate Discounts available

For batch schedule & course fee kindly contact at respective locations or email us info@cliplab.co.in