Diagnostics pharma service

Torramma
has extensive experience in applying the different genetic analysis methods and techniques which are crucial for the entire drug development and production process:

Preclinical phase through all phases of clinical trials (phases I, II and III)
Quality control for production of biologicals.
Comprehensive services available for all your study or project needs:

Analysis
Research
Development
These services are available from single sample analysis all the way through to the high throughput levels involving several thousand samples

All projects are discussed before providing a quotation to ensure a clear and precise understanding of your needs and requirements. Each project is planned thoroughly, with interim milestones scheduled, to ensure the highest probability for success.

Our pharma and diagnostic services will assist you to:

develop agents and drugs more efficiently and economically,
use them optimally and precisely regarding their effectiveness,
better avoid possible adverse effects and
ensure the safety of the compounds through quality control during their production.

Our regulated services cover in general (but are not limited to):

  • Assay development and validation
  • Scientific consultancy during the planning and implementation of analyses in the scope of clinical trials
  • Expert advice on the evaluation and interpretation of results
  • Quality assurance and quality management following GxP guidelines
  • GLP-grade documentation (study plan and final report)
  • Project consultancy and project management
Fill out this field
Please enter a valid email address.
Fill out this field
Menu