Leveraging early insights to accelerate the oral drug development cycle
28 May 2025
2:00pm
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This webinar explores oral drug product development and how to address critical challenges such as complex formulations and regulatory hurdles.
This webinar will explore the critical challenges and barriers that often slow down oral drug development. Join to learn about practical strategies and case studies for identifying and mitigating risks early, and how proactive planning can significantly accelerate development and ensure successful outcomes. Recommendations are also offered on how to avoid the most common barriers, speed up the development programme, save time and API.
Case studies will explore real-world examples of successful oral drug development projects that leveraged early insights for accelerated development.
Key learning points:
- Early risk identification: learn how to anticipate and address formulation, manufacturing, and regulatory challenges early in the development cycle
- Strategic formulation design: discover innovative approaches to designing effective oral formulations that meet both efficacy and safety standards
- Regulatory insights: understand the latest regulatory requirements and how to navigate them effectively to ensure compliance and approval.
Register your details to join >>>
OUR SPEAKER
Ramesh Muttavarapu – Global Subject Matter Expert – Technical and Scientific Affairs
Ramesh Muttavarapu is a global subject matter expert on oral solids forms. He has more than 20 years of industrial experience in developing and commercialising these dosage forms. He is experienced in formulating simple to complex dosage forms including multiparticulates. His multiparticulate experience includes fluid bed coating, extrusion and spheronisation, hot melt extrusion and mini tablets with tailored drug release profiles covering immediate, delayed, controlled and pulsatile.
Ramesh has developed numerous multiparticulate products, commercialised three products, and is the co-inventor of a patent on delayed release pellets. Ramesh earned his Bachelors and Masters in pharmaceutics from the University of Bangalore and University of Annamalai, India, respectively. Additionally, he earned an MBA from Linder College of Business, University of Cincinnati, OH, USA
FAQs
FAQs
Is the panel discussion free?
Yes – there is no charge to watch the panel discussion, either live or on-demand.
When will the panel discussion take place?
28 May at 3pm BST.
Can I watch it later?
The panel discussion will become available to watch on-demand shortly after the live webinar takes place.
What are the benefits of attending live?
You’ll be able to ask the speakers your questions, which will be answered live in the Q&A towards the end of the session.
How long will the panel discussion be?
This panel discussion will last up to an hour.
What do I need to watch this panel discussion?
All you need is a computer with an internet connection. We recommend using headphones if possible if you’re in an office environment.