Essential Strategies for Successful Pharmacovigilance and Post-Market Surveillance
4:00 PM – 5:30 PM, Central European Time (CET)
10:00 AM – 11:30 AM, Eastern Time (ET)
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Overview
Are you prepared for the challenges of getting your drug to market? The journey doesn’t end once your product is launched; it’s just the beginning.
Join our engaging webinar focused on mastering pharmacovigilance and post-market surveillance. Discover critical best practices that will ensure the long-term success of your products and operations. With the right knowledge and strategies, you can effectively navigate the complexities of ongoing safety monitoring.
Imagine having a robust pharmacovigilance program that meets regulatory requirements and protects your company from costly recalls and fines. Learn to identify key signals, triggers, and actions that should shape your post-market strategy. By attending, you’ll gain insights into building a best-in-class surveillance program tailored for pharma companies bringing their first products to market or those seeking to strengthen their existing practices.
Don’t leave your product’s future to chance. Register now to secure your spot in this essential webinar and empower your organization with the expertise needed to excel in pharmacovigilance and post-market activities.
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Who Should Attend:
- Quality Assurance Professionals
- Regulatory Affairs Professionals
- Skill Level: Novice, Intermediate
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Topics:
- Understand and apply the key elements of good pharmacovigilance practice (GVP)
- Learn how to build a best-in-class post-market surveillance program
- Understand the signals, triggers and key actions that should shape your post-market program
- Insulate your business from the risk of recalls and fines
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Special event information:
All participants will get a complimentary certificate of attendance courtesy of the webinar's sponsor - Qualio.
Speaker
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Dr. Manolo Ernesto Beelke (MD, PhD)Chief Medical Officer, Managing DirectorDr. Manolo Beelke brings over 28 years of extensive experience in clinical research with a focus on Neurology, Psychiatry, and Sleep Medicine. As an accomplished consultant and former Chief Medical Officer, he has designed and provided medical guidance for over 160 clinical trials and authored more than 40 peer-reviewed articles. Dr. Beelke holds an MD and a PhD in Sleep Medicine, along with board certifications in Clinical Neurophysiology and Sleep Medicine. His expertise in Clinical Development and Medical Affairs, combined with his leadership skills, positions him as a recognized authority in the field, making significant contributions to advancements in pharmaceutical practices.
Partner
Qualio
Website
https://qualio.com/Founded in 2012, Qualio is the first cloud quality management software for all Life Sciences companies. Medical device and pharmaceutical companies need a secure and scalable quality management system with the flexibility to support their evolving needs. Qualio meets that challenge by cutting through the complexity to optimize and automate critical quality processes. The remote-first, Qualio team is distributed across North America and Europe.
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Event Registration
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