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Double Feature: Highlighted Twice in Unict Magazine!

We are delighted to share with you an exciting update: our endeavors have been spotlighted not once, but twice in the esteemed pages of Unict magazine! Article #1: Delve into an exploration of Mimesis. From its conceptualization to its present iteration, uncover how innovation drives our progress. Article #2: Prepare for a momentous revelation! We have received significant updates from the European Medicines Agency (EMA) that promise to reshape our trajectory. Anticipate a transformative shift in our journey ahead. For a comprehensive insight, we invite you to peruse the complete features via the following link:https://www.unictmagazine.unict.it/ We extend our sincere gratitude to Unict magazine for the esteemed recognition, and we commend our dedicated team for their unwavering commitment. #DoubleFeature #UnictMagazine #Innovation #EMA #TeamEffort 🌟

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Pioneering the Future of Healthcare: Mimesis S.r.l. and the Universal Impact of Regulatory Support

Advancing Towards Regulatory Recognition: Mimesis S.r.l.’s Groundbreaking Effort In a world-first, Mimesis S.r.l., within the innovative In Silico World (ISW) Consortium (https://www.insilico.world), has secured preliminary regulatory acceptance from the European Medicine Agency (EMA) for its UISS-TB-DR simulation platform. This groundbreaking achievement not only marks a historic moment for tuberculosis (TB) vaccine development but also opens the door for a myriad of UISS engine-powered solutions to benefit from regulatory support. The EMA Letter of Support is publicly available following this link. Understanding the Milestone and Its Implications Preliminary Regulatory Support: The EMA’s initial support for the UISS-TB-DR platform acknowledges the innovative approach of Mimesis S.r.l. using the UISS engine. While this marks an important step forward, it comes with the responsibility to address specific limitations and gather additional data to fully meet regulatory standards. Encouraging Innovation with Caution: This phase of regulatory process underscores the importance of continued development and validation. Mimesis S.r.l. is encouraged to navigate these challenges with the aim of achieving full regulatory approval, reflecting a balanced approach to innovation and safety. Navigating the Path to Full Regulatory Approval The journey toward full regulatory approval is marked by this initial acknowledgment from the EMA, which recognizes the innovative potential of the UISS-TB-DR platform. As Mimesis S.r.l. works to address the outlined limitations and expand its research, this moment serves as a stepping stone for broader applications of the UISS engine in healthcare. The commitment to overcoming these challenges reflects a dedication to advancing medical science responsibly. A Collaborative Effort for Healthcare Innovation: Mimesis S.r.l., supported by the EMA’s guidance, is paving the way for future innovations in TB treatment and beyond. By addressing the specific feedback and expanding its data collection, Mimesis S.r.l. demonstrates its commitment to meeting the highest standards of regulatory compliance and medical efficacy.

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Mimesis is a new member of the Avicenna Alliance

It is an honour for us to have become part of this Alliance, which will certainly lead us to grow and learn a lot, both as a company and as people. Let us hope that this is the beginning of a long and worthwhile journey. Click on this link to find out more:https://avicenna-alliance.com/latest-news/news/mimesis-is-a-new-avicenna-member/