What are the AS9100 Required Documented Information?

When it comes to AS9100 certification, certain documents are essential. They prove an organization’s commitment to customer needs and product safety in the aerospace industry. Document control procedure is key to managing these documents. It explains how documents are made,

Documented Information

What Is The Difference Between Documented Information and Records?

Documented information is any knowledge or data created and stored in any format, like digital files, paper docs, or audio recordings. Records are a subset of this, identified as having long-term value and requiring formal control and management. They serve

What Is The Difference Between Document Control and Record Control?

Document control focuses on creating, reviewing, approving, and distributing documents. This includes making sure they are up to date and accessible to the right people. Version control is also part of document control, tracking different versions of a document. Record control,

What Are The Different Types of GMP Documentation?

GMP Documentation is the backbone of the pharmaceutical industry, ensuring quality and safety in medicines’ production. It covers many records, procedures and reports that document all aspects of the manufacturing process. What Are The Different Types of GMP Documentation?

What Is FDA 21 CFR Part 11 Compliance?

The FDA’s 21 CFR Part 11 compliance is essential for businesses in regulated industries. It guarantees the security and integrity of electronic records and signatures. Here, we investigate the key features of Part 11 compliance, such as scope, requirements, and

What Is The Difference Between Documents and Records In ISO 9001?

In ISO 9001, documents and records are often used interchangeably. However, these have distinct meanings and serve different roles in an organization’s quality management system (QMS). What Is The Difference Between Documents and Records In ISO 9001?

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