Difference between qualification and validation in the pharmaceutical sector
In the pharmaceutical industry, robust control of equipment, facilities and processes is essential to guarantee the safety of the […]
Data Integrity according to FDA, EMA and MHRA
Data Integrity is a central pillar in the pharmaceutical industry and in any regulated environment.
Design of clean areas for aseptic processes: GMP principles and current challenges
The design of clean areas for aseptic processes is one of the pillars on which the manufacturing of
Technical guide for the design, construction, validation and maintenance of pharmaceutical clean rooms
Regulatory compliance and contamination control strategies 1. Introduction to the modern pharmaceutical engineering paradigm The pharmaceutical industry
Why is risk key in the validation of automated systems?
In the pharmaceutical industry, automated control systems are the basis for the safe, efficient and reproducible operation of products.
GMP requirements for the qualification of water systems in pharmaceutical environments
In the pharmaceutical industry, water is one of the most critical services. Used as raw material, solvent, agent
AI and document control: automation of the life cycle of Standard Procedures
In a highly regulated pharmaceutical environment, where traceability, accuracy and regulatory compliance are non-negotiable, document management
What role does outsourcing play in today's pharmaceutical industry?
Productive outsourcing, also known as contract manufacturing, has been consolidated in the pharmaceutical industry as a central strategy for
How to ensure quality in engineering projects for the pharmaceutical industry
In the pharmaceutical industry, engineering projects must not only meet technical objectives and execution deadlines, but
Materials, regulations and trends in piping for the pharmaceutical industry
The design and installation of piping in the pharmaceutical industry are fundamental aspects to guarantee the quality of the products.