Supportive Services

For well over a decade now, device manufacturers, pharmaceutical companies,medical gas developers and biological specialists have been entrusting Inamed with their early phase clinical trials. Backed by our comprehensive on-site infrastructure, we provide the professional personnel necessary to design, execute and evaluate a broad spectrum of studies including first-in-man, bioavailability/ bioequivalence and proof-of-concept trials. An industry pioneer and leader in many disciplines, Inamed accompanies sponsors to the next level through decisive research data. In order to achieve this, we support our clients right from the beginning.

Services related to Clinical Studies

  • Consulting
  • Protocol development
  • Informed Consent Form development
  • Case report forms and diaries
  • Regulatory Affairs
  • Recruitment of patients, healthy volunteers or study sites
  • Feasibility Studies
  • Project management
  • Monitoring
  • Data management
  • Biometrics
  • Medical writing (e.g., IMPD, IB, CTR)
  • Quality Assurance and Auditing
Find further information on our Clinical Operations website

Consulting Services

  • Consulting: Project assessments, external clinical development expertise, additional clinical pharmacology expertise for complex project issues and crucial decisions (second opinion)
  • Concepts: Development strategy and concepts, life cycle management, drug rescue concepts, bio-pharmaceutical concepts, add-on expertise and resource in conceptual matters and study design issues
  • Medical and scientific writing: Study synopses, study protocols, IMPDs, CTDs, expert reports, publications
  • CRO selection and management: Support in identification and selection of specialized non-clinical and bioanalytical service providers, support in establishment of co-operations and partnerships
  • Education and training: Workshops and seminars in clinical pharmacology, pre-clinical/clinical interface, early drug development