Transforming Oral Drug Products for Late-Phase and Commercial Excellence
Webinar Date/Time: Tue, Dec 3, 2024 11:00 AM EST
Learn how to extend product life cycles through innovative reformulation strategies that enhance patient compliance and streamline late-phase manufacturing. Join BioDuro-Sundia's webinar to explore opportunities to boost product performance.
Register Free: https://www.pharmtech.com/pt_w/commercial-excellence
Event Overview:
Join BioDuro-Sundia’s exclusive webinar to discover cutting-edge technologies for extending product life cycles through innovative reformulation strategies. Learn from real-world case studies how to streamline late-phase drug product development and manufacturing and unlock new market opportunities with enhanced patient compliance. Gain actionable insights to overcome obstacles in late-phase development and manufacturing, such as scaling up production, ensuring regulatory compliance, and managing complex supply chains, and accelerate your product’s path to success. Don’t miss this chance to stay ahead in the competitive pharmaceutical landscape.
Key Learning Objectives:
- Learn strategies for transforming products to enhance release profiles.
- Practice techniques to boost patient compliance through optimized dosing strategies.
- Implement effective life cycle management strategies for late-phase manufacturing
Who Should Attend:
- Directors of research and development
- Senior product managers
- Procurement managers
- Heads of formulation development
- Vice Presidents of Manufacturing
- Chief scientific officers
- Directors of clinical operations
- Executive vice presidents of product development
Speaker:
Bhavishya Mittal, PhD
Vice President of Product Development and Manufacturing
BioDuro-Sundia
Bhavishya Mittal, PhD, is a pharmaceutical scientist with over 21 years of experience in formulation and process development for solid oral dosages targeting oncology, inflammation, gastrointestinal, and CNS indications. Mittal has worked with industry leaders such as BioDuro-Sundia, AbbVie, and Takeda, and is the author of 3 books and 4 US patents. His expertise includes product development strategy, project management, regulatory interactions, and quality by design implementation. He is dedicated to advancing drug development and enhancing industry practices.
Register Free: https://www.pharmtech.com/pt_w/commercial-excellence
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