With CQ’s Audit Management Software, we ensure companies have the ability to build a flexible, scalable and configurable audit management workflow. Depending on the specific needs of your organization, you can automate a rapid audit process or configure a workflow for a complex audit.

Create, schedule and manage your audit program using the calendar view available in the CQ Audit Management…

To improve health and safety in your enterprise and reduce the costs of avoidable illness and injury, companies must depend on good and timely data to focus on the areas of highest risk first and improve their health and safety program across the company.

Although a Health & Safety program is a very essential element, every workplace will need to adopt to safeguard its greatest asset – human resource – implementing a robust health & safety program gaining without the backing…

Change is everywhere, and can be initiated from anywhere in your organization. CQ Change Management software allows you and your supply chain partners to establish and follow best practice workflows to address the entire change management lifecycle. The software supports each aspect of your own change management process from initiation and review/approval through to execution tracking,…

GMP training is a requirement as it emphasizes employees performing all the tasks in accordance with GMP expectations and established procedures. GMP training is an essential requirement for pharmaceutical manufacturers as per 21 CFR 211.25 (a) – Personnel Qualifications. The GMP training is mandatory for both drug manufacturers and ingredient suppliers. Notably, GMP training and certification are considered a…

OSHA regulations are rules that describe the methods employers are legally required to follow to protect their workers from hazards. Before OSHA can issue a standard, it must go through a very extensive and lengthy process that includes substantial public engagement, notice and comment. The agency must show that a significant risk to workers exists and that there are feasible measures employers can…

Maintain a centralized repository of identified risks at the project, department, or company level with CQ Risk Management Software. Drive strategic decisions on potential threats with the solution that is aligned with the latest standards (ISO 31000, ISO 14971, ICH Q9 and risk principles in ISO 9001:2015, ISO 13485:2016, ISO 45001 and ISO 14001) to help accelerate assessments, identify and analyze risk trends and drive risk mitigation activities. Identify the right approaches that…

With CQ Document Management, you can manage the entire document lifecycle, gain complete visibility and rely on a single source of truth across all locations for more effective decision making.

Regulatory compliance is stringent. With an electronic approach to document management across the enterprise, you’ll have a central repository to create, modify, review, approve, store, organize, access…

Another critical component of OSHA is reporting. Employers in highly hazardous industries are mandated to keep records of serious work-related injuries and illnesses. OSHA’s record-keeping regulations are based on the framework from the national occupational safety and health record-keeping system. OSHA workplace safety adheres to a structured reporting requirement that…

Every company, no matter what services or goods it produces, must deal with three most important values: time, price and quality. Customers choose to do business with organizations that have the ability to deliver excellence in quality in a timeframe that they wish for, and at a price point that is affordable. One thing that stands out in the end is the quality of product, as the customer experience lasts longer than the time or the price. An organization needs to have next generation…

Salesforce safety - ComplianceQuest is an Enterprise Quality, Safety and Environment Management (QHSE) solutions platform natively built and run on Salesforce technologies. We help our customers of all sizes deliver quality products and services in the safest, most sustainable way by mitigating risk, problems, and inefficiencies while protecting customers, employees, suppliers, and brands.

In May 2018, FDA first proposed revising its current Quality System Regulations (QSR) under 21 CFR Part 820 to more precisely align with the international ISO 13485:2016 standard as the basis for its quality system legislation. This signals an essential step forward for the international standard, which is already used globally. FDA ISO 13485 QMS standard for medical devices enables controlling…

Corrective and Preventive Action (CAPA) process helps an organization to analyze and collect relevant product-related information, investigate and identify product and quality problems, and trigger appropriate and effective corrective or preventive actions to eliminate a problem and prevent its recurrence. CAPA has two different components, corrective action and preventive action. Corrective…

The enterprise-wide quality management system from ComplianceQuest has a module dedicated to documentation workflow automation through a document management system software.

Centralize all your incident data, near misses, safety observations, investigations for implementing agile corrective actions with ComplianceQuest’s Health and Safety Incident Management Software.

Furthermore, mitigate risks and prevent accidents by detecting a hazardous trend ahead of time using built-in analytics, predictive intelligence, dashboards, and mobile capabilities. By instilling an…

The CQ Document Management Software, being a part of its enterprise-wide quality management system, empowers you to automate and manage your entire document lifecycle. It provides you with complete visibility throughout the document lifecycle and improve your decision making by providing a single source of truth across all locations.

Regulatory bodies are becoming more stringent about…

Environmental health and safety management is an all-in-one term that focuses on improving the EHS performance of a business. EHS management refers to the implementation of procedures focused on ensuring and improving the safety of workers and their surroundings. These processes play a significant role in achieving and maintaining the overall environmental goals of the organization. EHS…

CAPA (Corrective Action, Preventive Action) is a methodological strategy for mitigating risks and improving processes, identifying the sources of actual or potential issues and their root causes, planning solutions for those problems, and documenting the solution so that similar issues don’t occur in the future. CAPA is a way to improve the company’s processes by taking a series of actions…

Being IATF 16949 compliant is not a regulatory requirement but can also benefit the businesses by improving processes and efficiency that drives cost savings. Besides ensuring customer satisfaction and improvement, some of the other advantages to get IATF 16949 certification include—

Reduced operating costs

Improved stakeholder relationships

Proven business…

Change management solution is a structured, determined approach aimed to transform people, teams, and organizations from their present state to the desired future state.

Change management solution is essential for below practices:

1. Eliminate ongoing failures during the change as an opportunity for learning and promote an organizational culture that supports it.

2. Stay open…

To maintain the greatest transparency and ethical conduct with clients, customers, employees, and stakeholders, organizations must have a compliance training program to reduce risks, keep everyone updated, maintain trust, and decrease the chances of violating the law.