Contact Sales Support Center
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.
The pharmaceutical industry requires compliance with Good Manufacturing Practices (GMP), data integrity requirements, and global regulatory frameworks. Against this backdrop, inspection readiness and audit...
Regulated industries have always been defined by strict documentation requirements, audit scrutiny, and an ever expanding library of records. As...
Whether just hearing the acronym QMS for the first time or evaluating software for small businesses, quality management systems are central to reliable operations and...
Interested in learning more about how ACE can help?