Academic Training in Clinical Research & Pharmacovigilance with Certification

We are excited to announce the launch of the Academic Training in Clinical Research & Pharmacovigilance with Certification, designed for professionals seeking to expand their expertise in both clinical research and pharmacovigilance, two critical areas in the healthcare and pharmaceutical industries. This program offers an in-depth understanding of clinical trials, regulatory compliance, and drug safety monitoring.

Course Overview: This dynamic program provides a comprehensive curriculum that integrates key concepts in clinical research and pharmacovigilance. Participants will learn how to design, manage, and evaluate clinical trials, as well as how to ensure drug safety and regulatory adherence throughout a product’s lifecycle – from pre-market clinical testing to post-market surveillance.

Key Topics Include:

• Clinical Research Fundamentals:
  • Clinical Trial Design and Methodology
  • Good Clinical Practice (GCP) Guidelines
  • Regulatory Requirements for Clinical Trials (FDA, EMA, ICH)
  • Ethical Issues and Patient Safety in Clinical Trials
  • Data Management and Clinical Trial Monitoring
• Pharmacovigilance Essentials:
  • Introduction to Pharmacovigilance and Drug Safety
  • Adverse Drug Reaction (ADR) Reporting and Management
  • Signal Detection and Risk Management Strategies
  • Global Pharmacovigilance Regulations (FDA, EMA, WHO)
  • Post-Marketing Surveillance and Risk Minimization
• Integration of Clinical Research and Pharmacovigilance:
  • Combining Clinical Data and Safety Data
  • Role of Pharmacovigilance in Clinical Trials
  • Best Practices in Managing Safety Data and Regulatory Compliance

Target Audience: This program is ideal for:

• Clinical Research Associates (CRAs) and Coordinators (CRCs)
• Pharmacovigilance Professionals
• Medical Affairs and Regulatory Affairs Specialists
• Healthcare Professionals
• Research and Development Teams
• Professionals looking to transition into clinical research or pharmacovigilance roles

Certification: Participants will receive Academic Clinical Research & Pharmacovigilance Certificates upon successful completion of the training, demonstrating their proficiency in both fields.

Why Choose This Training Program?

• Gain a deep understanding of clinical research and pharmacovigilance processes.
• Learn from experienced professionals and academic experts.
• Receive a recognized certification that boosts your career in clinical research and drug safety.
• Access a wealth of resources and case studies from leading industry practices.
• Networking opportunities with peers and professionals in the healthcare and pharmaceutical sectors.

Program Details:

• Duration: 3 months
• Format: onsite, 1.5 hours, 3 times a week, 17:00- 18:30 (GMT+4)
• Start Date: 17 March 2025
• End Date: 17 June 2025
• Language: English
• Fees: 100,000 AMD
• Registration Deadline: 07 March 2025
• Training Address: Avan, Duryan 1^st str. 10, Armenia
• Link for registration: https://forms.gle/tTZyKKFfjkxxdgLK8  

*Once you register, we will contact you for payment details

For any queries contact us: Dr. Liana Kasyan – (+374) 94 02 08 23, liana.kasyan@etl.am, kasyanliana@gmail.com

Training is a journey of growth, where the pursuit of knowledge meets the responsibility to protect lives. It reminds us that learning is the bridge between understanding and making a meaningful impact on the world.