Metronomia

METRONOMIA is your Data Science CRO for biostatistical services and consulting, clinical data management, and medical writing. Since 1990, we have supported over 650 projects in all clinical development phases and major therapeutic areas. Our team of 120+ highly skilled employees serves the needs of our pharma-, biotech-, and medical device customers with the highest degree of flexibility, reliability and quality.

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Locations

  • Africa
  • APAC
  • Australia
  • Europe
  • North America
  • South America

Therapeutic Areas

  • Cardiovascular
  • Covid-19
  • Dermatology
  • Endocrinology
  • Gastroenterology
  • Hematology
  • Hepatology
  • Immunology
  • Infectious Diseases
  • Medical Aesthetics
  • Neurology
  • Oncology
  • Ophthalmology
  • Orthopedics
  • Respiratory
  • Rheumatology
  • Urology
  • Vaccines
  • Woman's Health

ABOUT METRONOMIA

For over 30 years, METRONOMIA has been an exceptional CRO partner for biostatistical services and consulting, clinical data management and medical writing.

Our team of 120+ highly skilled and committed employees serves the needs of our customers with the highest degree of flexibility, reliability and quality.

Our clients are pharmaceutical, biotech and medical device companies. Over 650 successful projects in all clinical development phases and major therapeutic areas are a testament to our data science excellence and exceptional service quality!

WHY US?

  • Sustainable business relationships with >92% repeat business and a high staff retention rate.
  • Exceptional customer experience through personalized service, and open, honest and proactive communication.
  • Direct access to subject matter experts, statisticians, clinical data managers & medical writers enables maximum efficiency and adaptability to client needs.
  • State-of-the-art knowledge, processes & technology.
  • Size matters! Our clients experience METRONOMIA as the “right”-sized partner – which always gives the “right” attention to their projects.

SERVICES

Biostatistical consulting

  • Statistical and regulatory intelligence
  • Strategic study design planning
  • Statistical consulting based on state-of-the-art methods
  • Active involvement in scientific advice meetings
  • Modelling and simulation

Clinical data management

  • CDASH compliant eCRFs
  • Complete clinical data management package incl. data review & cleaning, medical review & coding, eCRF user management, helpdesk & support
  • Vendor oversight support
  • eCRF, ePRO, IRT, RTMS
  • Systems:
    • CLINCASE
    • RAVE
    • VIEDOC
  • Bespoke Clinical Data Warehouse solutions

Biostatistical services

  • Protocol and SAP development
  • Submission support
  • ISS & ISE analyses
  • Comprehensive DSMB/IDMC support
  • Randomization
  • Non-clinical statistical services
  • Vendor oversight support

Statistical programming

  • SDTM and ADaM datasets & submission ready CDISC packages
  • TFL programming and validation
  • Conversion of legacy data

Medical writing

  • Study protocols/ Clinical Investigation Plans
  • DSURs
  • CSRs, Clinical Investigation Reports & manuscripts
  • Submission dossiers
  • Medical writing
  • Study protocols/Clinical Investigation Plans
  • DSURs
  • CSRs, Clinical Investigation Reports & manuscripts
  • Submission dossiers
  • Non-clinical medical writing

IDMC support services

  • Independent data center services and secure data storage/exchange
  • Acting as central point of contact for sponsor and IDMC members
  • Statistical services for interim analyses
  • Management of committees including contracts, remuneration and meeting minutes

Partnered Full-Service and Tailored Service Packages

Trial Rescue Services

Accreditations

Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.