Quality by Design (QbD) in Pharmaceuticals
The pharmaceutical industry is evolving rapidly, with increasing regulatory demands, complex drug formulations, and the rise of biologics challenging traditional manufacturing methods.
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How can companies stay ahead while ensuring efficiency, quality, and compliance?
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This white paper delves into Quality by Design (QbD) and Design of Experiments (DoE)—two transformative methodologies that are revolutionising drug development.
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Learn how top pharmaceutical companies like Strides Pharma leverage these approaches to enhance product quality, reduce risks, optimise processes, and streamline regulatory compliance.
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Get insights on:
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✔️ QbD’s shift from reactive testing to built-in quality
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✔️ DoE’s role in faster, smarter drug formulation
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✔️ A real-world case study on arthritis medication development
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