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GMP

GUIDELINES FOR QUALITY ASSURANCE

GMP (Good Manufacturing Practice) covers guidelines for quality assurance in production procedures and surroundings in the manufacture of medicinal and active pharmaceutical products.
Quality assurance plays a central part in the manufacture of pharmaceuticals, as any deviations in quality in this area can have direct effects
on consumers' health.

A GMP-compliant quality management system serves to ensure product quality and compliance with the requirements set by the health authorities for the sale of products. The laboratory rooms must be constructed to cleanroom class B, C or D, must contain smooth surfaces for disinfection and hygiene
and also pressure level systems so that the air-borne particles meet the cleanroom classes.

GMP-COMPLIANT PRODUCT SAFETY

ROOM REQUIREMENTS acc. to GMP

// Clean room class B, C and D laboratory rooms
// Pressure level systems
// Hygienic and smooth surfaces
// Sluices

REQUIREMENTS ON THE MONITORING SYSTEM

// GMP-compliant system for the monitoring of all relevant parameters
// Central system for the recording of all parameters
// Extremely simple user operation
// Unambiguous and clear alarm function
// Safe storage of all quality-related data (long-term archive)
// Alarm/visualisation in the cleanroom

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Building Information Modelling (BIM)

Building Information Modelling provides new approaches for the planning and realisation of both construction projects and the operation of buildings. 
The HT Group supports users of the BIM method with modules and interfaces in the planning. Our BIM components are being continuously developed and adjusted to the latest state of technology. Revit components for your BIM model can be requested using the following contact form. ?We will be happy to answer any questions you may have on the subject of BIM planning.

Revit-Part for BIM-Model

BIM EN
Model*