EloquiMed Logo

Webinars & Events

Join our expert-led webinars to enhance your knowledge of medical writing, regulatory affairs, and clinical documentation best practices.

Upcoming Webinars

Mastering Clinical Study Reports: From Data to Document

Mastering Clinical Study Reports: From Data to Document

Learn the systematic approach to transforming clinical data into comprehensive, compliant study reports. This webinar covers best practices for organizing raw data, collaborating with statisticians, and creating narratives that meet regulatory requirements.

June 15, 2025
11:00 AM EDT (60 minutes)
Presented by Dr. Sarah Johnson, Director of Medical Writing
Regulatory Strategy for Emerging Biopharma

Regulatory Strategy for Emerging Biopharma

Essential regulatory considerations for early-stage biotech companies developing novel therapeutics. This session covers regulatory pathways for innovative therapies, developing an effective regulatory strategy, and efficient document preparation for successful interactions with regulatory authorities.

May 28, 2025
1:00 PM EDT (45 minutes)
Presented by Michael Chen, VP of Regulatory Affairs
AI-Enhanced Medical Writing: Practical Applications

AI-Enhanced Medical Writing: Practical Applications

Real-world examples of how AI is being ethically implemented in medical and regulatory writing. Learn about compliant AI usage, maintaining scientific integrity, and how AI tools can enhance documentation quality while reducing time-to-submission.

May 14, 2025
10:00 AM EDT (60 minutes)
Presented by Dr. Alisha Patel, Senior Medical Writer & AI Specialist

Past Webinars

Missed one of our webinars? Browse our archive of past events and access recordings to catch up on valuable insights and strategies shared by our experts.

Streamlining the Protocol Development Process

Streamlining the Protocol Development Process

Effective strategies for creating clinical trial protocols that balance scientific rigor with operational feasibility.

April 10, 2025
Dr. Marcus Wong, Clinical Development Director
Watch Recording
Global Pharmacovigilance Requirements

Global Pharmacovigilance Requirements

Navigating the complex landscape of international safety reporting and risk management documentation.

March 22, 2025
Elena Rodriguez, Head of Pharmacovigilance
Watch Recording
Effective Investigator Brochures

Effective Investigator Brochures

Best practices for developing clear, comprehensive IB documents that support clinical trial success.

March 5, 2025
Dr. James Chen, Medical Director
Watch Recording
Common Technical Document (CTD) Best Practices

Common Technical Document (CTD) Best Practices

Strategies for organizing and preparing high-quality CTD submissions for regulatory authorities.

February 18, 2025
Dr. Samantha Lee, Regulatory Affairs Director
Watch Recording
Patient-Focused Medical Writing

Patient-Focused Medical Writing

Techniques for creating clear, patient-friendly documentation for clinical trials and healthcare materials.

January 30, 2025
Dr. Emily Johnson, Patient Communications Specialist
Watch Recording
Regulatory Intelligence for Medical Writers

Regulatory Intelligence for Medical Writers

How to stay current with evolving regulations and effectively incorporate requirements into documentation.

January 15, 2025
Michael Thompson, Senior Regulatory Specialist
Watch Recording

Need a Custom Webinar for Your Team?

We offer private webinar sessions tailored to your organization's specific needs and challenges. Contact us to discuss customized training for your medical writing and regulatory affairs teams.

By subscribing, you agree to our Privacy Policy. You can unsubscribe at any time.