Infrastructure

      Pharmaceutical development laboratory

      Laboratorio de Desarrollo Farmacéutico

      Modern facilities for the optimal galenic and analytical development of drugs, together with stability chambers in all conditions, allowing us to carry out ICH studies of all kinds.

      We provide formulation solutions in different pharmaceutical forms: solids (tablets, capsules, etc.), liquids (suspensions, solutions, etc.), and semi-solids (gels, creams, etc.).

      Description

      We have more than 3,500 m2 for the pharmaceutical industry and extensive experience in developing a wide variety of drugs.

       Solid pharmaceutical forms:

      • Rotary and eccentric compression machine
      • V mixer
      • High speed mixer / granulator
      • Fluid bed
      • Coating pan
      • Capsule filler
      • Extruder/ spheroniser
      • Spray-dryer
      • Freeze-dryer
      • Voluminometer
      • Rotolab

      Liquid and semi-solid pharmaceutical forms:

      • Paddle stirrer
      • Ultra-Turrax homogeniser
      • Colloid mill
      • Rheometer
      • Viscosimeter
      • Osmometer

       Control equipment:

      • Analytical balance and moisture analyser
      • Durometer
      • Friability tester
      • Disintegrator
      • Dissolution test equipment and fraction collector
      • Granulometric analysis equipment based on laser diffraction and Coulter

      Other equipment:

      • Biosafety cabinet
      • Differential scanning calorimetry (DSC)
      • Primary packaging equipment (blister packaging machine)

      Aimed at:

      • Pharmaceutical laboratories.

      Certifications and Recognitions

      AEMPS
      The Pharmaceutical Development Control Laboratory is certified by the Spanish Agency for Medicines and Healthcare Products (AEMPS) in Good Manufacturing Practice (GMP) guidelines: Physical and chemical quality control medicines for human use and medicines under research.
      AEMPS
      The manufacturing plant is certified by the Spanish Agency for Medicines and Healthcare Products (AEMPS) in Good Manufacturing Practice (GMP) guidelines: Manufacture and import of pharmaceuticals for non-sterile human use, including psychotropic and narcotic substances / Manufacture and import of non-sterile investigational medicinal products.
      ISO 13485
      The drug manufacturing plant has been granted the ISO 13485 certification for quality management for the medical devices industry.