Amidst the array of tools available to assist Life Science companies in managing their operations, the Electronic Quality Management System (eQMS) emerges as a crucial cornerstone for ensuring adherence to regulatory mandates. Notably, the eQMS shines when it comes to meeting the requirements of 21 CFR Part 11, encompassing aspects such as validation processes, time markings, the upkeep of digital records, and electronic duplicates. Moreover, it plays a pivotal role in aligning with 21 CFR Part 820, which delineates the necessary practices for maintaining high manufacturing standards, especially in the realm of medical devices.
The eQMS seamlessly connects the dots between ongoing document and process updates, providing a comprehensive trail that covers the entire lifecycle of each piece of documentation. Supported by established procedures and project models, the eQMS stands as a reliable solution, ensuring validation and enhancing the overall efficiency of the organization’s operations.
A quality system for you and your company
Harnessing the Potential of eQMS Across Your Organization
The comprehensive features and capabilities of an Electronic Quality Management System (eQMS) can be leveraged by your entire company to consistently fortify both the organization and its products. This encompasses document management, risk assessment, training, audits, corrective and preventive actions (CAPAs), as well as facilitation for other quality-related processes. The eQMS is a tool for everyone, fostering alignment throughout the company and product spectrum while providing clarity on roles and responsibilities.
Engaging Colleagues Beyond Quality Assurance
Here's how you can pique the interest of your colleagues outside the Quality Assurance realm:
1.
What’s in it for me:
Foster involvement by initiating conversations with end users from various segments of the company. Ask them, “What tools or features would enhance your daily tasks and streamline your workload?”
2.
Defining Roles and Responsibilities:
The eQMS is structured around individual roles within the organization, ensuring a clear delineation of responsibilities. This safeguards colleagues by granting access only to authorized personnel.
3.
Enhanced Accountability and Transparency:
The eQMS grants insights into the timing and contributors behind comments, inputs, and alterations in documents. This trail of information promotes traceability, accountability, and heightened visibility.
4.
Seamless Administration and System Integration:
Merging the eQMS with other systems yields a comprehensive overview of the entire organization. Integrations hold intrinsic value by adding efficiency and reducing costs.