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Minimize potential risks associated with IMP quality and regulatory compliance in your EU-based QP clinical trials by utilizing Zenovel's experienced local QP oversight for batch release. Our meticulous approach ensures adherence to all QP release clinical trials guidelines, safeguarding the well-being of trial participants and the integrity of your research data.
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Tired of complex formatting? Zenovel offers a meticulously designed CTD dossier template in an easily editable Word format, tailored to meet the specific requirements of both the US FDA and the EU EMA. Streamline your regulatory submissions and ensure compliance with a professional and well-structured CTD dossier.
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Partner with Zenovel for dedicated and exceptionally comprehensive QMS support in your journey to establish a world-class qms system in pharma. We are steadfastly committed to empowering your organization to achieve the absolute highest standards of quality, unwavering regulatory compliance, and demonstrable operational excellence through the strategic implementation of a robust and meticulously tailored quality management system designed specifically for the pharmaceutical sector in Ahmedabad, Gujarat, India, and beyond.
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