Asset Manager

Updated:

CorEvitas

CorEvitas runs clinical registries within PPD, part of Thermo Fisher Scientific, providing longitudinal real-world patient data for pharmaceutical...

CorEvitas

CorEvitas operates as a clinical registry business within Thermo Fisher Scientific's PPD clinical research organization. The unit was originally established as CorEvitas before being acquired by PPD and later folded into the Thermo Fisher ecosystem upon PPD's acquisition in 2021. Its registries track longitudinal, real-world patient data to inform clinical trial design and post-market safety assessments. The strategy involves collecting standardized clinical and patient-reported data from practicing physicians across multiple disease states for pharmaceutical sponsors. Registries capture data on disease progression, treatment persistence, and outcomes, generating evidence used for label expansions, health technology assessments, and regulatory commitments. CorEvitas collaborates with Evidera, PPD's real-world evidence arm, to offer observational studies, safety monitoring, and implementation science, addressing therapeutic areas including rheumatology, dermatology, and gastroenterology. PPD employs approximately 30,000 professionals globally across clinical development, laboratory services, and real-world evidence. CorEvitas contributes within the real-world evidence segment, providing proprietary longitudinal data drawn from multiple disease-specific registries. The registries have supported academic manuscripts and conference presentations, including at ASCO 2026. No separate staffing or AUM figures are disclosed for the CorEvitas unit alone. CorEvitas holds a structural advantage through integration with PPD's broader infrastructure and Thermo Fisher's funding stability. Its registries offer longitudinal, standardized data that pharmaceutical clients cannot replicate independently. The unit's governance sits within PPD's clinical research hierarchy rather than as an independent investment vehicle, distinguishing it from venture-backed registry companies.

General information

Firm type

Asset Manager

Year founded

AUM

Undisclosed

Location

Region

North America

Country

United States

City

Waltham

Corporate office

Waltham, MA, United States

Sector focus

Healthcare Services

Frequently asked questions

Who owns CorEvitas?

CorEvitas is a business unit within the PPD clinical research organization, which Thermo Fisher Scientific acquired in 2021 (per Thermo Fisher, 2021).

What data does CorEvitas provide?

CorEvitas operates independent longitudinal registries capturing clinician- and patient-reported data on disease treatment patterns, outcomes, and safety. Its datasets cover 20-plus years and are used for regulatory submissions and trial design (per the firm's website).

How does CorEvitas compare to other real-world evidence providers?

Unlike aggregators reselling claims data, CorEvitas collects standardized, longitudinal data directly from clinicians through disease-specific registries. Its regulatory-grade data supports FDA and EMA submissions, positioning it alongside firms like IQVIA and ICON (per the firm's emphasis on regulatory evidence).

What therapeutic areas does CorEvitas focus on?

The firm's registries cover inflammatory conditions, including rheumatology, dermatology, and gastroenterology, with additional presence in oncology, as indicated by its ASCO participation (per the firm's website).

Does CorEvitas accept external investment or partnerships?

CorEvitas is not an investment vehicle but licenses its registry data to pharmaceutical companies under subscription or service agreements. It does not publicly disclose co-investment structures (per the firm's commercial model).

What is PPD's relationship to CorEvitas?

CorEvitas operates as a brand within PPD's clinical research division, alongside Evidera Real-World Evidence. PPD markets CorEvitas registries as part of its proprietary real-world data offerings (per the firm's website).

Are CorEvitas registries used for regulatory approval?

Yes. The firm states its regulatory-grade data supports post-approval commitments, label expansions, and safety assessments by regulators like the FDA and EMA (per the firm's website).

Profile maintained by using OSINT (open-source intelligence), regulatory filings, licensed data partners, and verified direct submissions. Read the methodology. Last updated: . Continuous refresh with full update cycles at least every 30 days.

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