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Catawba Research
Catawba Research
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Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
Maintenance & Renewals
Compliance
Transparency & Disclosure
Commercialization *
Customer Engagement
Brand Planning & Activation
Market Access & Policy *
Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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About
470 James Street, Suite 232, New Haven, CT 06513, USA
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Catawba Research
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Delivering Trusted Clinical Trial Management
Catawba Research is acontract research organization that provides clinical trial management services to the pharmaceutical, device, formulation development, and biotechnology industries. With a focus on conducting and managing clinical trials in accordance with ICH-GCP and regulatory requirements, Catawba leverages scientific leadership and therapeutic expertise to enable efficient, agile study delivery. Backed by an experienced team and active Scientific Advisory Board, Catawba serves as a trusted CRO partner known for innovative trial management and specialty expertise across a range of agency approvals and therapeutic areas.
As a global CRO taking on today's clinical trials in a new way, Catawba is committed to confidently advancing client programs with integrity, passion, accountability, and teamwork.
Delivering Trusted Clinical Trial Management
Catawba Research is acontract research organization that provides clinical trial management services to the pharmaceutical, device, formulation development, and biotechnology industries. With a focus on conducting and managing clinical trials in accordance with ICH-GCP and regulatory requirements, Catawba leverages scientific leadership and therapeutic expertise to enable efficient, agile study delivery. Backed by an experienced team and active Scientific Advisory Board, Catawba serves as a trusted CRO partner known for innovative trial management and specialty expertise across a range of agency approvals and therapeutic areas.
As a global CRO taking on today's clinical trials in a new way, Catawba is committed to confidently advancing client programs with integrity, passion, accountability, and teamwork.
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470 James Street, Suite 232, New Haven, CT 06513, USA
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