GxP compliance software is critical in industries including pharmaceutical, biotechnology, and medical devices as it helps ensure adherence to strict regulatory standards and guidelines that govern the production, distribution, and quality of products.

Ensures Regulatory Compliance – GxP guidelines (e.g., Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP)) are designed to ensure product safety, efficacy, and quality. GxP compliance software helps organizations meet the requirements of regulatory bodies including the FDA, EMA, or WHO by streamlining processes, maintaining accurate records, and enabling efficient audits.

Improves Data Integrity – Accurate and tamper-proof data is essential in regulated industries. GxP software ensures compliance with standards like ALCOA+ (Attributable, Legible, Contemporaneous, Original, Accurate, and Complete) to maintain reliable and trustworthy records for all operations.

Streamlines Documentation Management – Regulatory compliance often involves managing vast amounts of documentation, including standard operating procedures (SOPs), batch records, and testing data. GxP software centralizes document management, reduces manual errors, and simplifies version control, approvals, and retrieval.

Reduces Risk – Non-compliance with regulatory standards can lead to product recalls, financial penalties, legal liabilities, and damage to brand reputation. GxP compliance software mitigates these risks by providing automated controls, validations, and real-time monitoring to ensure operations remain within compliant boundaries.

Facilitates Audits and Inspections – GxP software maintains detailed, accurate, and audit-ready records. This makes it easier for companies to demonstrate compliance during inspections and audits by regulatory authorities.

Enhances Operational Efficiency – Automating compliance processes such as monitoring, reporting, and training reduces the manual workload, enhances productivity, and allows employees to focus on innovation and other value-added activities.

Supports Global Market Access – Compliance with GxP guidelines is often a prerequisite for market authorization in different regions. GxP compliance software ensures adherence to international standards, enabling companies to expand their market reach.

Ensures Patient Safety and Product Quality – Ultimately, the primary goal of GxP compliance is to protect patients by ensuring that products are safe, effective, and of high quality. Software solutions help organizations achieve this by maintaining rigorous control over processes and quality standards.

The EVOM™ Auto GxP Compliance Module is a powerful solution designed to help GMP/GLP laboratories achieve FDA 21 CFR Part 11 compliance with secure, traceable, and audit-ready electronic records when using our EVOM Auto 96 or 24 system. By integrating advanced security controls, this module ensures data integrity, authenticity, and system access protection, helping labs meet regulatory requirements with confidence.

Key compliance features include user-configurable password strength controls and timed password expiry, limiting system access to authorized individuals (21 CFR 11.10(d), 21 CFR 11.200(a)). User privileges are fully configurable, ensuring that only approved individuals can sign off on electronic records, preserving data authenticity and traceability (21 CFR 11, Subpart B). A built-in emergency access protocol prevents workflow disruptions by allowing authorized recovery of locked-out accounts (21 CFR 11.200(3)). Additionally, seamless integration with Windows Active Directory logins and passwords enforces controlled access management (21 CFR 11.10(d)).

The EVOM™ Auto GxP Compliance Module enhances security by detecting and recording unauthorized access attempts, ensuring that only users with valid credentials can access the system. With operational and authority checks, specific actions or sequences can be automatically disabled to maintain system integrity. For audit and security purposes, every electronic signature is permanently associated with its corresponding record, including the date, time, and reason for approval, providing full transparency and traceability.

By implementing the EVOM™ Auto GxP Compliance Module, labs can simplify compliance, strengthen data security, and confidently meet regulatory expectations while maintaining operational efficiency.