Two Types of Documentation Used To Manage and Record GMP Compliance

What Are The Two Types of Documentation Used To Manage and Record GMP Compliance?

Are you confused about the various types of documentation involved in GMP compliance? You’re not alone. With strict regulations and evolving practices, it can be overwhelming to keep track of all the required documentation. In this article, we will explore

What Is GMP Document Control?

Document control in the context of Good Manufacturing Practices (GMP) is a structure for organizing documents. Its goal? Ensure compliance with regulations. Implementing processes for creating, reviewing, approving, distributing and maintaining documents throughout their lifecycle is how it’s done. What

What are GMP Good Documentation Practices?

Good Documentation Practices (GDP) are key in GMP to ensure compliance, traceability, and accuracy. Clear and accurate documentation helps maintain product quality and safety during manufacturing. Promptly record info, use approved formats, and ensure proper review and sign-off. What are

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?

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