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Competence Centers   

FOCUS Neuss
FOCUS Moscow & Belgrade
FOCUS Laboratories
FOCUS Biomarkers
FOCUS Biometrics
FOCUS Immunology
PDM / Product Development Management
FOCUS Japan
FOCUS Indonesia
FOCUS ME & India
FOCUS Regulatory Affairs
MCS / Formulation
FOCUS Quality Assurance

FOCUS Core Competencies


Phase I-II Clinical Studies:

  • Global development perspectives - EU/USA/JAPAN
  • Phase I - complete range of full service clinical pharmacology studies conducted in own unit in  Neuss (100 beds) and in Moscow and Belgrade
     
  • Phase IIa - Fast Proof of Concept: access to large patient pools (incl. treatment-naive patients) at our locations in highly populated areas
  • Bridging strategies Japan - EU/US, Phase I studies in healthy Japanese volunteers in Germany
  • Late clinical pharmacology studies in special patient populations like renal/hepatic impairment, PK in patients
  • Access to large volunteer/patient pool   
  • Phase IIb and III studies in Western / Eastern Europe and Asia 
  • Highly experienced medical staff in clinical pharmacology & immunology
  • Biomarker research & immune-monitoring: The FOCUS Immunology Laboratory in Heidelberg generates added value to immunology and biomarker projects. www.focus-biomarker.de
  • Bioequivalence studies with Western quality standards and low costs at FOCUS Equilab in Jakarta, Indonesia

In Early Drug Development:

  • Product Development Management packages: We support our clients from the “idea” up to clinical Proof of Concept – special service for biotech companies or pharma’s second line products. The outcome is a high quality early clinical development package for either out licensing or further development to Phase III. www.pharma-development.com
  • Pharmaceutical expertise for preclinical and early clinical development: Formulation Development, drug targeting, preclinical formulatio preparation, cGMP handling of clinical trial supplies (own Qualified Person) and drug import www.microcarriersystems.com
  • Development of regulatory strategy and regulatory support by in-house regulatory affairs professionals
  • Cooperation with external experts (toxicology, pharmacology, EMEA)
  • Strategic product consultancy and development planning for new clinical entities and biological entities, herbal products, generics plus, drug combinations (FDC) and medical device products