Equipment qualification is the process of verifying and documenting that equipment, facilities, and systems are suitable for their intended use and operate consistently within their specified range of parameters. It is an important aspect of ensuring product quality and regulatory compliance in various industries such as pharmaceuticals, biotechnology, medical devices, and food manufacturing. The equipment …
Data integrity refers to the accuracy, completeness, and consistency of data throughout its lifecycle. In other words, data integrity ensures that data is reliable, trustworthy, and has not been altered or manipulated in any way.Data integrity ensures that research findings are reliable and can be reproduced by other scientists. To maintain data integrity, organizations must …
Regulatory compliance refers to the adherence to laws, regulations, and standards that apply to a specific industry or organization. Compliance is essential to avoid legal and financial consequences, maintain reputation, and ensure the safety and well-being of stakeholders. To achieve regulatory compliance, organizations must identify and understand relevant laws and regulations, develop policies and procedures …
Regulatory audits are an important tool used by government agencies to ensure that organizations comply with laws and regulations. These audits are typically conducted by auditors who have been trained to assess an organization’s compliance with applicable laws and regulations. During a regulatory audit, auditors will typically review an organization’s policies and procedures, as well …
