Preparation and readiness of GMP and regulatory inspections
Автор: Pharma GMP News
Загружено: 2025-12-23
Просмотров: 33
Practical advice for preparation and readiness of gmp and regulatory inspections
This guide provides comprehensive strategies for pharmaceutical and medical device companies to maintain constant regulatory readiness and successfully navigate health authority inspections. It outlines various audit types—such as pre-approval, routine, and for-cause visits—while emphasizing that the primary goal is ensuring patient safety and product efficacy. The text details essential personnel roles, including Subject Matter Experts (SMEs), escorts, and scribes, who collaborate to manage the flow of information and documentation. Practical advice is offered on inspection etiquette, such as honesty and brevity, alongside technical requirements for setting up dedicated inspection and war rooms. Additionally, the source addresses modern challenges by providing a framework for virtual inspections, focusing on IT infrastructure and remote communication protocols. Ultimately, the author advocates for a proactive approach to compliance to mitigate the significant risks and costs associated with reactive remediation.
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