Phoenix Pharma
LabWare
BA Unternehmensgruppe
Reckitt
BIONTECH
ratiopharm
SANOFI
Boehringer Ingelheim
Biotest
Heraeus
Takeda
HAYS
UMM
STORCK
Torrent Pharma
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Consultancy services to develop comprehensive strategies for maintaining Audit Readiness status of the Quality Management Systems (QMS). We provide the necessary documentation outlining the strategy to ensure continuous compliance and readiness for future audits (e.g.: FDA and EMA). Through meticulous planning and strategic guidance, we empower clients to proactively manage their QMS and uphold high-quality standards.
We collaborate with clients to develop a strategy for maintaining Audit Readiness within their existing QMS framework. Our team outlines clear objectives, milestones, and action plans to address potential gaps and ensure ongoing compliance with regulatory requirements.
Zamann assists clients in creating the necessary documentation to support the Audit Readiness strategy, including policies, procedures, checklists, and templates. We ensure that all documentation aligns with regulatory standards and best practices, providing clear guidance for implementing and maintaining an audit-ready QMS.
Our team provide training and guidance to client teams on the use and maintenance of QMS documentation, ensuring effective implementation of the audit readiness strategy across the organization. We conduct workshops and training sessions to educate staff on the importance of Audit Readiness and equip them with the necessary skills to uphold compliance standards.
Our team collaborates closely with you to create, maintain and improve your Quality Management Systems ensuring a perfect fit between processes and goals. From initial setup to ongoing support, we ensure that every element supports robust holistic compliance, efficiency, and long-term growth.
Zamann is committed to building Quality Management Systems that exceed expectations. With a deep understanding of regulatory requirements and global practical expertise, we ensure not only compliance with regulations, but also optimization of QMS´s workflows and continuous improvement.
