TrialTop Logo
#
Abacus International
United Kingdom
About
Services
Therapeutic Expertise
Founded in 1995, Abacus International started life as a specialist health economics consultancy. Since then, we have evolved into a global provider of integrated market access services. In this time, the market access landscape for pharmaceutical and medical devices companies has changed immeasurably. Payers, and not prescribers, have become the primary decision makers; health technology assessment (HTA) bodies have emerged worldwide; and, most recently, we have seen the trend towards value-based pricing in place of free or reference pricing. As our environment has changed, however, Abacus International has always innovated and adapted to our surroundings – evolving our market access consultancy offering to meet the ever-changing needs of our clients. Today, our integrated market access services deliver effective health economic and evidence-based solutions across the product lifecycle: Payer Insight and Reimbursement Strategy – plan for success Systematic review – evaluate the evidence Health economics – develop cost-based value argument Clinical outcomes assessment – Develop and validate patient-centred outcome measures Health technology assessment – achieve positive recommendations Value communication – maximise access & uptake Strategic market access planning & consultancy

Do you work for Abacus International?

Type

Likely Type

Founded

1997

Number of employees

51-200

Number of employees

website_link

#

Lorem Ipsum is simply dummy text of the printing and typesetting industry.

Lorem Ipsum is simply dummy text of the printing?

#####

Your headline

  • Lorem Ipsum is simply dummy text of the printing and typesetting industry.

  • rambled it to make a type specimen book.
    Benefit 1

  • Benefit 2

  • Benefit 3

Clinical Directory

Clinical Software

Provide digital tools like EDC, ePRO, and telemedicine platforms to manage clinical trials, streamline data, and ensure regulatory compliance.

  • Electronic Data Capture (EDC)

  • ePRO (Electronic Patient-Reported Outcomes)

  • eConsent Platforms

  • Telemedicine Platforms (eVisits)

  • Clinical Trial Management Systems (CTMS)

  • Data Analytics and Real-World Evidence

  • Regulatory Compliance Software

Clinical Research

Offer services for conducting clinical trials across phases, from preclinical to post-marketing, helping companies accelerate drug development.

  • Preclinical CROs (Animal studies, toxicology)

  • Phase I CROs (First-in-human studies, safety)

  • Phase II CROs (Efficacy, small patient groups)

  • Phase III CROs (Large-scale trials, effectiveness)

  • Phase IV CROs (Post-marketing surveillance)

  • Full-Service CROs (End-to-end solutions for all phases)

Clinical Development

Handle drug development and manufacturing, including API production, formulation, and large-scale commercial manufacturing.

  • API Manufacturing (Active Pharmaceutical Ingredients)

  • Drug Product Formulation and Development

  • Clinical Trial Material Supply

  • Commercial Manufacturing

  • Biologics Manufacturing

All rights reserved. Blueprint.io