Germany – Pharmaceuticals

GMP-compliant cleanroom solutions for the pharmaceutical industry in Germany

ISO 7 / ISO 8 modular cleanroom systems | CE certified | EU GMP Annex 1

✔ Modular design
✔ Integrated HVAC
✔ Validation-ready

Are you facing these challenges in pharmaceutical production?

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Strict EU GMP Annex 1 requirements

Precise pressure cascades & air exchange rates

Control of particles and germs

HVAC systems with validation requirements

Short project durations for new construction or expansion

Our modular solution for pharmaceutical cleanrooms

GMP-cleanroom

Areas of application:

API Production

Sterile filling

Secondary packaging

Controlled storage areas

Technical highlights:

dersion Modular structure

ISO 7 / ISO 8 classification

ce

CE-compliant construction

h14

HEPA H14 Filtersysteme

cleanroom hvac system

Integrated HVAC systems

Cleanroom display screen

Temperature and humidity control  |  Differential pressure control

“Technical expertise for the highest cleanroom standards”

― DERSION
制药洁净室布局图(1)
  • icons8-play-50Layout optimization for production flow

    icons8-play-50Material and personnel separation

    icons8-play-50Documentation support for IQ/OQ

    icons8-play-50Risk analysis according to GMP

Your advantages with Dersion in Germany

DERSION CLEANROOM

Our Team

  • 20 years of cleanroom experience | Modular design for faster assembly | International project management | Support with validation documentation | Cost-optimized solutions without compromising quality

Transparent project process

Consulting → Layout Design → Manufacturing → Delivery → Installation → Validation Support

Trust Section

CE Certification
ISO Manufacturing Systems
Technical Drawings & Documentation Packages
International Reference Projects

“International Pharmaceutical Cleanroom Projects”

― DERSION
GMP分布
GMP-Reinraum
GMP-Reinraum

Medical cleanroom

Business area: Cardiovascular and cerebrovascular interventions, implantable medical devices, surgical robots, endoscopic imaging systems, etc.

Area: 304 m²

Cleanliness: GMPC compliant

Temperature and humidity: Temperature controlled at 18–26 °C, relative humidity controlled at 45–65% RH

Cleanroom for biopharmaceutical products

Area: 420 m²
Cleanliness: Class 1000 (ISO 6)
Temperature: 20–26 °C
Humidity: 40–65% relative humidity

Reinraum für biopharmazeutische Produkte
Reinraum für biopharmazeutische Produkte

Cleanroom for biopharmaceutical products

Area: 900 m²
Cleanliness: Class 10000 (ISO 7)
Temperature: 23 ± 3 °C
Humidity: 30–60 %

Reinraum für biopharmazeutische Produkte
Reinraum für biopharmazeutische Produkte

“Start your GMP cleanroom project today”

  • 1. Free technical consultation / 2. Tailor-made offer / 3. Layout planning included

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