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06, November de 2024

AUDIT OF COMPUTERIZED SYSTEMS IN THE PHARMACEUTICAL INDUSTRY: SECURITY AND REGULATORY COMPLIANCE

This article is complemented by: Validação de Sistemas Computadorizados Validação de Sistemas Computadorizados Agile e CSA By Gustavo Soares and Thiago Borin Evaluation based on GAMP 5, 21 CFR Part 11, and the […]

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23, October de 2024

AI and ML in the Pharmaceutical Industry

Implementation of AI and ML in the Pharmaceutical Industry: Impact, Standards, and Guidelines By Gustavo Soares Abstract With the advancement of Artificial Intelligence (AI) and Machine Learning (ML) in the pharmaceutical industry, new […]

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16, October de 2024

FDA Form 483

The FDA Form 483, issued by the Food and Drug Administration (FDA), is an official document used by the agency to communicate to a company the conditions or practices observed that may violate […]

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02, October de 2024

ABNT NBR 16328:2024 and ISO 17665:2024 norms update

ABNT NBR 16328 and ISO 17665 are essential standards for the sterilization of healthcare products, specifically for measuring temperature, humidity, and pressure in thermal equipment. Both standards were updated in 2024, reflecting advancements […]

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11, September de 2024

FDA Warning Letter: What It Is, Common Reasons, and How to Respond Properly

FDA Warning Letter: What It Is, Common Reasons, and How to Respond Properly An FDA Warning Letter is an official alert indicating that a company has violated significant regulations that could affect the […]

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