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Modular white room vs. Conventional construction: when to choose each

Raúl Fernández October 9, 2026 No Comments

The choice between a modular clean room and a conventional construction depends on critical factors such as the lead time, the necessary flexibility, the possibilities of expansion and the technical…

Types of doors for clean rooms: features and how to choose them

Roberto Navarro October 2, 2026 No Comments

White room doors are a critical architectural element within any controlled environment environment. Far from being simple points of passage, they directly intervene in the control of contamination, the tightness…

<strong>Laminar flow cabins</strong> and its sterilization and disinfection

Laminar flow cabins and its sterilization and disinfection

Raúl Fernández September 22, 2026 No Comments

When we deal with cleanroom issues, processes that require a controlled and aseptic environment, cleanliness is one of the most important points to touch. But, in sectors and circumstances in…

why and how to get the <strong>GMP Certification</strong>

why and how to get the GMP Certification

Raúl Fernández September 8, 2026 No Comments

Any product that affects people's health, that is, is consumable, so that it can go on the market, it must meet a series of quality standards. These standards are complied…

Autoclave in the laboratory: types, uses and regulations of sterilization

Raúl Fernández July 22, 2026 No Comments

The autoclave is one of the most critical equipment in highly regulated laboratories, hospitals and industries. It is a team that uses high pressure and temperature water vapor to sterilize…

White room monitoring: Control of differential pressure, particles and temperature

Roberto Navarro June 26, 2026 No Comments

White room monitoring consists of continuously measuring and recording critical environmental parameters, such as particle concentration, differential pressure, temperature and humidity, to ensure compliance (GMP/ISO) and safeguard the integrity of…

GMP cleanroom in the pharmaceutical industry: design, requirements and validation

Raúl Fernández June 18, 2026 No Comments

A GMP Pharmaceutical cleanroom is a controlled environment designed to minimize contamination during drug manufacturing. Its design, construction and validation must comply with the GMP guidelines and guarantee specific conditions…

Biosafety levels BSL 1, 2, 3 and 4: what they are and what they contain

Raúl Fernández June 5, 2026 No Comments

The biosafety levels They are an internationally standardized containment scale that dictates the physical barriers, protective equipment, and operational practices necessary for working with biological agents. The objective of this…

GMP in pharmacy: differences with the standard laboratory

Raúl Fernández May 20, 2026 No Comments

GMP Good Manufacturing Practices (GMP) is the quality system that regulates how medicines are manufactured to ensure their safety, efficacy, and traceability. Unlike a standard laboratory, a GMP laboratory operates…

What is biosecurity? Levels, standards and application in the laboratory

Raúl Fernández May 6, 2026 No Comments

The Biosafety It is the set of rules, measures and practices aimed at preventing biological risks and protecting the health of people, the environment and laboratories. It is applied especially…

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