Change Control System is an integrated approach that transforms teams, people, and organizations from their current state to their preferred future state. The objective of a Change Control System is to help employees understand, embrace, commit, and accept changes in their current business environment.

Training Compliance Management refers to handling or tracking various training modules that companies must mandate to ensure all employees are trained in their area of work, understand the processes of the company, and remain compliant with various regulations mandated by OSHA, ISO, or FDA. Training Compliance Management Solution allows businesses to identify training gaps, missed deadlines, and…

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.

EHSQ encompasses laws that govern processes, professionals, and workplace behaviors. It effectively manages your environmental, health, safety, and quality aspects to reduce incidents that impact the product quality and direct and indirect costs due to injuries. By automating the EHSQ processes using an integrated software system such as the one from ComplianceQuest, you can…

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 Management (Environment, Health and Safety) is a crucial aspect of an enterprise’s operations.

Quality managers use ISO 13485 audit checklist to determine if the QMS aligns with the ISO 13485 software standard requirements. The ISO 13485 audit checklist is used for internal audit while preparing the system for a third-party ISO 13485 certification audit. The ISO 13485 audit checklist allows quality managers to document evidence of compliance based on processes, standard…

With CQ CAPA Management Software, you can identify and initiate a corrective and/or preventive action process, detect trends, conduct or link to an existing investigation and root cause analysis (RCA), define action plans to change or improve, and ensure effectiveness checks with a structured verification and closure.

With CQ CAPA Management Software, you can identify and initiate a corrective and/or preventive action process, detect trends, conduct or link to an existing investigation and root cause analysis (RCA), define action plans to change or improve, and ensure effectiveness checks with a structured verification and closure.

OSHA safety standards are focused on protecting the workforce’s safety and health while also providing training, outreach, education, and assistance to employers.
As workplace complexity and health & safety risks have increased over the years, the OSHA safety standards guidelines too have evolved.

The EQMS from ComplianceQuest facilitates manufacturing companies with product design, managing costs, from supplier management to input quality, complaint handling to continuous improvement. ComplianceQuest’s next-generation manufacturing QMS software enables you to be compliant with GMP standards such as ISO 9001 and US FDA.

The life sciences quality management system is crucial for regulatory compliance, continuous product improvement, and managing all documentation and workflows. ComplianceQuest’s next-generation life science quality management software is designed with exceptional features and functionalities.

GMP refers to the Good Manufacturing Practices that consist of processes, procedures, and documentation. It can help to avoid recalls and fines and also reduce losses and waste. GMP addresses problems around cleanliness, handling complaints, valid process usage, sanitation and hygiene, record keeping, and employee qualifications. It also ensures the safety, purity, and effectiveness of its products by taking proactive measures. Manufacturers can understand how to implement…

Every automotive industry needs an effective and robust Quality Management System in place to detect, monitor, and address the product issues before introducing the product to the market. By following the industry best practices across the organization, ComplianceQuest’s automotive quality management software enables automotive manufacturers to meet compliance and operational…

The medical device audit checklist allows quality managers to document evidence of compliance based on processes, standard requirements, and process characteristics.

ISO 13485 that was initially published in 1996, underwent significant revisions in 2003 and again in 2016, including changes in guidelines that apply specifically to suppliers and manufacturers of medical device…

The internal audit procedure for manufacturing company focuses on improving process flows, cybersecurity, and the organization’s overall efficiency.

Any organization with a compliance management program must regularly conduct internal audits. These audits assure that the business operates at maximum efficiency across all departments.

Internal audits for…

Internal Audit in Pharmaceutical Industry operations is a standard part of most quality system plans today. There are many different ways to complete internal auditing. Once it is done completely, you can assess the internal control of a system and measure the effectiveness of the quality system. A systematic, disciplined approach can accomplish an organization’s…

Periodic workforce health and safety audits are conducted as an effective way of identifying workplace hazards. An ongoing process that needs to be undertaken periodically, these workplace health and safety management system audit checklist are used to rate a company’s health and safety program, identify its strengths and weaknesses, and highlight areas that…