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PPD

by Thermo Fisher Scientificthermofisher.com
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OVERVIEW

A leading global Contract Research Organization (CRO) providing comprehensive drug development and clinical trial services, underpinned by proprietary AI-enabled digital solutions.

PPD, the clinical research business of Thermo Fisher Scientific, is a leading global Contract Research Organization (CRO) providing broad, integrated drug development, laboratory, and lifecycle management services to pharmaceutical, biotechnology, medical device, academic, and government organizations. The company, founded in 1985, operates in nearly 50 countries with over 40,000 employees.

Core Technology Platform: Preclarus™ The PPD service is heavily underpinned by its proprietary technology platform, Preclarus™. Preclarus is a comprehensive clinical data solution that consolidates and standardizes data from multiple sources—including Electronic Data Capture (EDC), Interactive Voice/Web Response Systems (IVRS/IWRS), and central lab data—to provide transparent, real-time access to clinical trial operations and patient data. This allows researchers, sites, and study monitors to make faster, more-informed decisions and enables advanced research approaches like risk-based monitoring and adaptive trial designs.

Key Digital Solutions & Capabilities:

  • Preclarus Central Lab Database: A proprietary web-based enterprise and information management system for central lab operations, providing real-time access to lab data and results.
  • Preclarus Investigator Site Portal: A web portal and mobile application that provides clinical trial sites with tools for patient management, sample collection logistics, kit ordering, and reviewing laboratory results.
  • Clinical Trial Forecasting Suite: An advanced AI-powered platform leveraging deep learning models and proprietary data to enhance forecasting accuracy, optimize clinical trial planning, and predict milestones.
  • Intelligent Clinical Suite: Sophisticated AI solutions designed to enhance the speed, quality, and resource efficiency of clinical trials through a comprehensive approach to study execution and data management.
  • Full-Service CRO Offering: Capabilities cover early development, all phases of clinical development (Phase I-IV), peri- and post-approval, and comprehensive laboratory services.

The PPD clinical research business focuses on applying cutting-edge technologies and therapeutic expertise to accelerate innovation and increase drug development productivity for its customers.

RATING & STATS

User Rating
4.5/5.0
Customers
1,000+
Founded
1985

KEY FEATURES

  • Real-time Clinical Trial Data Access (via Preclarus™)
  • AI-Powered Clinical Trial Forecasting & Optimization
  • Integrated Central Lab Data Management
  • Investigator Site Portal and Mobile Application
  • Risk-Based Monitoring and Adaptive Trial Designs
  • Full-Service Clinical Development (Phase I-IV)
  • Patient Recruitment and Retention Solutions

PRICING

Model: enterprise
PPD provides custom-tailored solutions and pricing based on the scope of clinical development, laboratory, and lifecycle management services required for the client's drug development program. Pricing is not publicly disclosed.

TECHNICAL DETAILS

Deployment: cloud, saas
Platforms: web, ios, android
📱 Mobile Apps🔌 API Available

USE CASES

Full-Service Clinical Trial Execution (Phase I-IV)Central Laboratory Services and Data ManagementDrug Discovery and Development OutsourcingReal-World Evidence (RWE) GenerationPost-Approval and Lifecycle Management

INTEGRATIONS

Medidata Platform (Rave, Adjudicate)CTMS (Clinical Trial Management System)EDC (Electronic Data Capture)IVRS/IWRS (Interactive Voice/Web Response System)OpenAI (Collaboration for AI solutions)

COMPLIANCE & SECURITY

Compliance:
HIPAAGDPRFDA 21 CFR Part 11ISO 27001
Security Features:
  • 🔒2FA
  • 🔒SSO
  • 🔒Encryption
  • 🔒Access Controls

SUPPORT & IMPLEMENTATION

Support: email, phone, dedicated account manager
Implementation Time: 1-3 months
Target Company Size: medium, enterprise
TRAINING AVAILABLE

PROS & CONS

✓ Pros:
  • +Global scale, reach, and comprehensive therapeutic expertise.
  • +Proprietary, integrated technology platform (Preclarus™) for real-time data access.
  • +Strong focus on AI and predictive analytics for trial optimization.
  • +Part of the Thermo Fisher Scientific ecosystem, providing end-to-end solutions (CRO + CDMO + Lab).
✗ Cons:
  • -No public product reviews for the core technology platform (Preclarus™).
  • -Enterprise-only model, not suitable for small-scale or individual software use.
  • -Employee reviews sometimes cite high workload and stress, which can indirectly impact service delivery.

ABOUT THERMO FISHER SCIENTIFIC

Other software by Thermo Fisher Scientific:
Ion Torrent (Cancer Genomics & Precision Oncology PlatformsTumor-normal sequencing analysis)
Oncomine Pan-Cancer Cell-Free (Cancer Genomics & Precision Oncology PlatformsLiquid biopsy analysis platforms)
Oncomine Pan-Cancer MRD (Cancer Genomics & Precision Oncology PlatformsMinimal residual disease (MRD) monitoring)
Oncomine Tumor Mutation Load (Cancer Genomics & Precision Oncology PlatformsTumor mutational burden (TMB) calculation)
Thermo Fisher LIMS (HL7 Interface EnginesError handling and monitoring)