How to Prepare for an OSHA Inspection - ComplianceQuest QHSE Solutions

An inspection by OSHA, whether announced or unannounced, can be a cause for much stress and concern. The stress is often caused by fear of the unknown and the implications to your enterprise from any violations. But does it have to be so?

ISO 9001 is a standard that facilitates the incorporation of best practices into an enterprise’s Quality Management System (QMS). Compliance to ISO 9001 needs automation and digital technology like ComplianceQuest’s holistic QHSE system.

Documents are an essential part of every business and can take many forms. At any enterprise, documents can include contracts with suppliers, customers, employees, and guidelines for governance.

Documents form an essential part of an enterprise’s journey. Document management is also essential as part of regulatory compliance for quality and safety.

21 CFR Part 11 is the FDA guideline that defines the criteria under which electronic records and electronic signatures are considered to be trustworthy, reliable and equivalent to that of the paper records. Part 11, as it is commonly known, was introduced in 1997 and applies to FDA-governed industries that choose to store their primary, authoritative records electronically.

CQ’s Inspection Management Solution streamlines inspection-related processes within your organization such as receiving, in-process, shipment and product returns.

CQ’s Sustainability Management System, a key solution within CQ EHS platform, enables organizations to easily and effectively manage to collect, track, analyze, trend and report the key sustainability performance indicators.

Managing your suppliers today can be a global challenge, whether you’re a manufacturing, consumer goods, energy or highly regulated life sciences operations. CQ Supplier Management is built specifically for every function in your company that’s impacted by and works with your supply chain.

CQ’s Equipment Management Software empowers businesses by simplifying equipment management by tracking, scheduling, maintaining calibration, performing regular maintenance activities and reporting.

ISO 13485 standard is an effective solution to meet the comprehensive requirements for a Quality Management System. It provides a practical foundation for medical device companies to address Medical Device Directives, regulations and responsibilities as well as demonstrating a commitment to the safety and quality of medical device products.

CQ’s Nonconformance Management Solution provides the required framework to capture, triage, investigate and disposition all nonconformances in a timely and effective manner.

CQ Training Management allows you to train employees in a timely fashion, and keep your workforce skilled with constantly evolving changes in the environment.

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.

With CQ CAPA Management, 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.

CQ Change Management allows you and your supply chain partners to establish and follow best practice workflows to address the entire change management lifecycle.

Audit management software system designed to manage your end-to-end process in a faster and effective way to increase your productivity by decreasing manual documentation.