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This workshop will focus on the currently most relevant topics in the CMC (Chemistry, Manufacturing and Controls) Regulatory space within the global pharmaceutical/ biopharmaceutical arena, including reliance and global regulatory convergence, post-approval changes to COVID-19 vaccines and treatments, impact of digitalisation in CMC submissions, updates on global ICH Q12 implementation & training, challenges with innovative therapies, global case studies on medical devices and combination products, and many other topics.
The format will allow participants to engage in constructive dialogue with experts from Regulatory Agencies, International Organisations and Industry, enabling interactive cross-functional discussions.
CONNECT WITH EXECUTIVES, HEAD, MANAGERS...INVOLVED IN…
- CMC Regulatory Affairs
- CMC Policy
- Global Development
- Quality Assurance/Quality Control
- Quality Intelligence
- Regulatory Compliance
- Regulatory Policy
- API Development and ManufacturingS1S
- Formulation Development and Manufacturing
- Analytical Development
- Technical Research and Development
- ICH Guidelines implementation and development
- CMC Lifecycle Management
- CMC Project Management
- Medical Devices and Combination Products
….and many more!
Share your case study, product or services from your organization, and interact directly with the audience through the below items (not limited to):
- On-demand sponsored sessions
- Podcasts
- Lunch & learn
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