How to Digitally Optimize Comparability for More Effective Post-Approval Change Management

Maria Batalha (Consultant) will present the webinar How to Digitally Optimize Comparability for More Effective Post-Approval Change Management on Mar 12, at 8:00 AM EDT. There is a second session at 12:00 PM EDT.

Post-approval changes are inevitable in the pharmaceutical industry, whether due to tech transfers, the introduction of new suppliers, or other lifecycle updates. As a result, comparability exercises are critical to ensure product quality, safety, and efficacy. Traditional manual processes are slow and resource-intensive. Cloud-based digital solutions transform these exercises by integrating data, automating workflows, and leveraging AI and analytics for faster, more informed decision-making. With regulatory expectations rising and data complexity increasing, adopting a digital approach is essential for efficiency and ICH Q12 compliance.  

Join this webinar to discover how digital optimization streamlines comparability, enhances audit readiness, and accelerates change management. Register now to stay competitive in a rapidly evolving regulatory landscape.

Even if you are not able to attend the live event, we still recommend registering in order to receive a link to the full recording.

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