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The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) has introduced several mandatory requirements, from adverse event reporting and facility registration to product listing and safety substantiation, all of which require robust documentation and traceability. PSC Software offers eQMS and inspection management solutions to help organizations meet these and other regulatory requirements like ISO 22716 and EC Regulation 1223/2009. These solutions enable businesses to maintain product quality and adapt to changing demands of the cosmetics market.
ACE centralizes and automates critical quality processes through validated workflows. ACE also provides real-time document control, ensuring that product specifications, safety data, and SOPs are always current and accessible, supporting MoCRA’s record access requirement. Robust CAPA and deviation management workflows are also available to keep critical quality events on track.
Access continuously updated global regulatory information straight from ACE. Track product registrations, health authority interactions, and submission timelines in one platform, with onboard data analytic options and customizable dashboards for clear visualization.
ACE provides the tools to integrate quality across every stage of the product lifecycle.
ACE solutions are designed to help you produce safe, high-quality dietary supplements efficiently. Scale your operations with ease and stay agile to meet evolving industry demands and regulations.
ACE’s cloud-based platform offers scalable solutions tailored to fit your business needs, ensuring you have the tools to drive success at every stage.
Whether you’re a growing startup or a large enterprise, ACE adapts to organizations of all sizes with customizable features and workflows.
As your business expands, ACE grows with you—offering seamless upgrades and advanced functionalities to handle increased complexity and demand.
In regulated industries such as life sciences, pharmaceuticals, and medical devices, quality management is a strategic necessity. Manual processes, paper-based systems,...
In regulated industries like medical devices and life sciences, strong quality management is essential. An Electronic Quality Management System (eQMS) helps organizations maintain compliance,...
The life sciences sector is accelerating toward a future where quality and compliance are continually optimized. Two forces are driving this...
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