YOUR CLEANROOM SOLUTION

FOR THE

PHARMACEUTICAL INDUSTRY

Why Cleanrooms Are Critical in Pharmaceutical Production

The pharmaceutical industry is constantly evolving, facing emerging public health challenges. Recent global events have underscored the need for reliable, local drug manufacturing capabilities.

To combat medication shortages, new production facilities are being re-established in France and across Europe. In this context, sterile production environments are a top priority.

The manufacturing and testing of pharmaceutical products must take place in controlled cleanroom environments, regulated by strict international standards and guided by the principle of one-way workflow (also known as “forward flow”).

Pharmaceutical cleanrooms must comply with Good Manufacturing Practices (GMP) to ensure product integrity, safety, and traceability.

Your Goals: Safety and Compliance in Pharmaceutical Cleanroom Environments

Maîtriser-la-contamination-bactériologique,-microbiologique-et-particulaire

Prevent product contamination during production

Controle ultrastrict des particules en suspension

Protect operators and the working environment

Réguler le taux de brassage et de renouvellement d’air

Control air change rates and airflow patterns

Réaliser des zones de process de classe A B C D

Define and maintain classified zones (Classes A, B, C, D)

Your Goals: Safety and Compliance in Pharmaceutical Cleanroom Environments

Prevent product contamination during production

Protect operators and the working environment

Control air change rates and airflow patterns

Define and maintain classified zones (Classes A, B, C, D)

Disinfection, sterility and compliance

of your pharmaceutical cleanroom

Pharmaceutical cleanrooms must meet the strictest standards defined by global health authorities such as (ANSM, FDA, …). Manufacturers must demonstrate excellence in process control, product handling, documentation, and compliance management.

Traceability, risk mitigation, and non-conformity management are everyday requirements in this sector.

Case Study: For one of our long-standing pharmaceutical clients, a global leader in vaccine production, we designed and installed a sterile cleanroom featuring custom-made laminar flow, ensuring maximum air purity across their production line.

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Our advice for your tailor-made pharmaceutical cleanroom

Following a detailed assessment of your operations and regulatory requirements, we provide a tailored cleanroom solution optimized for your pharmaceutical processes.

We address every critical aspect:

Adapter for airflow ensuring the required dust class
Compliance with forward-flow principles for personnel and materials
Pressure cascade management between zones
Temperature and humidity control
Consideration of ATEX risks (explosive environments or chemicals)
Hygienic cleanroom architecture for easy maintenance and low particle retention

We also recommend essential cleanroom equipment and systems:

Air showers for decontaminating personnel and materials
Pass-through chambers for controlled material transfer
Decontamination airlocks (SAS)
Laminar flow for sterile production zones
Advise you on monitoring (GTC) and communication solutions

Our mission: Deliver pristine air quality, ensure process sterility, and improve your energy efficiency.

Our top priority: The sterility and compliance of your pharmaceutical production environment.

Learn More About Our Cleanroom Solutions

Your Future Pharmaceutical Cleanroom

Euroflux supports your project from initial consultation to turnkey installation of cleanrooms, clean zones, or controlled atmosphere areas (ZAC) classified as A, B, C, or D per ISO 14644-1.

We design a complete pharmaceutical cleanroom or laminar flow equipment to meet the requirements of your sector:

Weighing booths: For volatile product dosing in production zones
Sampling booths: For testing volatile products in logistics areas
Laminar flow : For transport, filling, capping, or packaging (liquid or solid forms)
Airlocks (SAS): With electric or mechanical interlock
Partitioned SAS: For handling bulk packaging (pallets, Octabins, etc.)
Pass-throughs: For secure material entry and exit
Waste management systems: Integrated via SAS or pass-throughs
Air showers : for decontaminating personnel and product flow
Containment cabins: Offering triple protection (product, personnel, and environment)

Euroflux integrates all technical components to ensure your cleanroom is fully compliant, efficient, and ready for operation. Our expertise also extends to medical devices, cosmetics, and chemical sectors.

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