CRISPR-Cas Defense Mechanism

CRISPR, Cas, defense, mechanism, genome, editing, molecular, biology, microbial, immunity, gene, manipulation, bioinformatics, experimentation, ethical, considerations, regulatory, frameworks, biotechnology, medicine, agriculture, research, innovation, technology, hands-on, learning, practical, skills, career, opportunities

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MODE
Online/ e-LMS
TYPE
Self Paced
LEVEL
Moderate
DURATION
1

Program Aim

The aim of this program is to provide participants with an in-depth understanding of the CRISPR-Cas defense mechanism, empowering them to explore its intricate workings, its applications in genome editing, and its implications across various fields.

About Program

This program offers a comprehensive exploration of the CRISPR-Cas system, from its natural origins to its revolutionary applications in genetic engineering. Participants will delve into the molecular mechanisms underlying CRISPR-Cas, examining its role in microbial immunity and its potential for targeted genome editing. Through lectures, case studies, participants will gain practical experience in utilizing CRISPR-Cas tools for gene manipulation and genetic engineering.

Program Objectives

  1. Explore the molecular mechanisms underlying CRISPR-Cas systems.
  2. Understand the natural role of CRISPR-Cas in microbial immunity.
  3. Examine the applications of CRISPR-Cas technology in genome editing and gene manipulation.
  4. Develop practical skills in designing and conducting CRISPR-Cas experiments.
  5. Analyze experimental data and interpret results using bioinformatics tools.
  6. Discuss the ethical considerations and regulatory frameworks surrounding genome editing.
  7. Foster critical thinking and problem-solving abilities in the context of genetic engineering.
  8. Prepare participants for careers in academic research, biotechnology, medicine, and agriculture.

Program Structure

1.CRISPR-Cas: Overview
2.Adaptive and heritable immune system of prokaryotes
3.Current Innovations of CRISPR- Cas Systems
4.Applications of CRISPR-Cas System
5.Project Report Submission/ Article Writing

Program Eligibility

Pharmacists and Pharmacy Technicians,Clinical Researchers,Regulatory Affairs Professionals,Medical Officers and Healthcare Providers,Quality Assurance Personnel

Program Outcomes

  • Comprehensive understanding of CRISPR-Cas defense mechanisms.
  • Proficiency in designing and implementing CRISPR-Cas experiments.
  • Ability to analyze CRISPR-Cas data and interpret experimental results.
  • Familiarity with ethical considerations and regulatory frameworks in genome editing.
  • Critical thinking and problem-solving skills in the context of genetic engineering.


Fee Structure

Standard Fee:           INR 11,998           USD 200

Discounted Fee:       INR 5999             USD 100

Certificate

Program Assesment

 

  1. Written Exams: Participants may take multiple-choice quizzes and written exams that test their knowledge of pharmacovigilance principles, regulatory requirements, and adverse drug reaction (ADR) management.
  2. Case Studies: Detailed analyses of real-world scenarios involving drug safety issues are used to assess participants’ ability to apply theoretical knowledge practically. This could involve identifying potential ADRs, proposing monitoring strategies, and suggesting mitigation actions.
  3. Group Projects: Collaborative projects where participants work in teams to design a pharmacovigilance program for a hypothetical or real drug. This assesses their ability to apply risk management principles and use pharmacovigilance tools effectively.
  4. Practical Simulations: Interactive sessions where participants use pharmacovigilance software to monitor and analyze data, simulating the role of a pharmacovigilance officer in a controlled environment.
  5. Research Papers: Participants may be required to write papers or reports on specific aspects of pharmacovigilance, such as comparative studies of international regulatory frameworks or evaluations of new methodologies in drug safety monitoring.
  6. Oral Presentations: Presentations to peers and instructors on topics related to pharmacovigilance, demonstrating participants’ understanding and ability to communicate complex information clearly.
  7. Peer Reviews: Assessment may also include peer-to-peer evaluation during group activities and discussions, fostering a deeper understanding through collaborative learning.

Future Career Prospects

  1. Pharmaceutical Industry Expansion
  2. Biotechnology Sector Opportunities
  3. Increased Focus on Clinical Trials
  4. Regulatory Bodies and Health Authorities
  5. Global Health Initiatives
  6. Academia and Research Institutions
  7. Consulting and Contract Research Organizations (CROs)
  8. Technological Innovations

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