QUALITY RISK MANAGEMENT

Prioritizing risk management increases patient safety and product quality

RISK DEMO ON-DEMAND

Risk Management System – Digital and Integrated

Proactively manage risks of pharmaceuticals, medical devices and other products with TrackWise Digital. The built-in templates comply with ISO 14971 and ICH Q9 allowing manufacturers to manage risks throughout the entire product lifecycle directly within TrackWise Digital.

Risk Management Datasheet

Risk Analysis

Integrated top-down and bottom-up risk assessments, such as the Hazard Analysis and FMEA, for holistic quality and product risk management.

Residual Risk

Visualize severities, occurrences and residual risks on a risk matrix to facilitate evaluation of the overall residual risk and benefit.

Production and Post-Production Review

Improve existing risk assessments and evaluations through data gathered throughout TrackWise Digital.

About Risk Management Systems

Webinar

An Integrated Approach to Quality Risk Management

Industry experts from Axendia and Honeywell discuss the value of quality risk management and its practical applications.

Blog

6 Signs of a Flawed Risk Management Process

The ability for the risk management process to create long term quality value for manufacturers is hindered by legacy processes that are a messy result of ad-hoc changes and hasty compliance initiatives.

Datasheet

TrackWise Digital Risk Management

Risk Management Connected to the QMS

Datasheet

Medical Device Risk Management

Effectively Manage Medical Device Risks With TrackWise Digital

Blog

Beyond Compliance: The Benefits of Integrated Risk Management

To reduce harm to patients and users, quality risk management must successfully integrate with the quality management system.

White Paper

Quality Risk Management: A Data-Driven Approach

Insights into the methods and benefits of digitally integrating a quality risk management program to the quality management system.

Risk Management and Quality Integrated With TrackWise Digital

Proactive risk reduction

Increase patient safety and improve product and process quality with effective risk management visibility across the organization and supply chain, allowing manufacturers to quickly prevent or mitigate quality issues.

Built on TrackWise Digital

Ensure all risk-based decisions and actions within the QMS are handled using consistent criteria for risk analysis, evaluation, control and acceptability of residual risks. Leverage data from core TrackWise Digital quality processes.

Risk Management for the Entire Lifecycle

Manage risks from concept development to production and post-production with a living risk management file that reflects the latest data from the QMS and the supply chain.

TrackWise Digital Risk Management System Testimonials

The outcome is clear. An integrated Quality and Risk Management program can maximize the use of QMS data supporting enhanced Risk Management and mitigation and improved product quality that delivers the maximum benefit to the patient.

Axendia

Dan Matlis | President

Risk Management System Capabilities

Supporting Quality Risk Management for ICH Q9 and ISO 14971

Risk Management File

Risk registry provides traceability of each hazard through risk analysis, evaluation, and control for specific products, product families, or a product platform. Electronic signatures and audit trail functionality, in accordance with 21 CFR Part 11.

Risk Analysis

Hazards Analysis and Failure Mode and Effects Analyses (for Use, Design, and Process) for a complete risk analysis. Save time and resources when building a risk analysis for similar new products, or product line extensions, with the ability to leverage portions of existing risk analysis into a new risk analysis.

Risk Evaluation and Control

Consistent risk evaluations to determine risk control. Track risk control activities for completion with team assignments and due dates. Evaluate residual risks to monitor risk reduction after risk control measures have been implemented.

Overall Residual Risk

Visual representation of individual residual risks on a risk matrix shows graphical distribution of the risks and facilitates evaluation of the overall residual risk and benefit.

Nonconformance and CAPA

Nonconformance and CAPA records directly linked to individual residual risks within the risk management file to aid in root cause analysis.

Production and Post-Production

Collect information throughout the product’s lifecycle to improve accuracy of the risk evaluations, signal detection and benefit-risk analyses.