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Worldwide Clinical Trials - Worldwide Evidence

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Northbrook, Illinois, US

About Worldwide Clinical Trials - Worldwide Evidence

Worldwide Evidence is the real-world evidence, health economics, observational research unit of Worldwide Clinical Trials, a global CRO.

We offer a unique blend of resources and perspectives, proven expertise, and innovative solutions throughout the entire continuum of a product’s lifecycle — from pre-launch into the real world.

Advancing Science and Strategy

The Worldwide Evidence team averages over 25 years industry experience in clinical research, real world evidence development, health economics and outcomes research. Focusing on the unique strategic, operational and regulatory challenges and opportunities inherent in peri- and post-approval research, we have earned an unparalleled reputation and record of success in research design and implementation to establish the clinical, economic, and humanistic value of our clients’ products.

Our Services (9)


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Observational Research/ Non-Interventional Studies

Price on request

Observational Research

Non-interventional studies
Patient registries
Post-Approval safety surveillance
Disease and product registries
Regulatory consulting
Patient Reported Outcomes


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Pharmacovigilance and Post-Authorization Safety Studies (PASS)

Price on request
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Health Economics and Outcomes Research (HEOR)

Price on request

Health Economics / Outcomes Research

Economic modeling
Cost of illness studies
Cost-effectiveness studies
Comparative effectiveness research
Patient-reported outcomes research
Systematic reviews and meta analysis
Strategic planning


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Marketing, Communication & Graphic Design Services

Price on request

Putting Evidence to Real World Use

Combining unique industry experience with in-depth functional expertise, our global team provides a broad spectrum of medical communications, strategic services, and execution support to identify and address the needs of diverse stakeholders involved in the delivery and reimbursement of healthcare. We believe strongly that medical product companies have an obligation to convey evidence of product value and safety both responsibly and persuasively.

Our goal and our clients’ goal is to achieve measurable results from effectively planned, relevant research initiatives.

Communications

Scientific platform development
Medical writing
Core claim and message development
Advisory panel development and support
Strategic publications planning and management

Market Access

Market analysis
Needs assessment and insights research
Payer and patient research and engagement
Value dossier development
Key account management strategy and materials

Medical Education

Healthcare professional community development and engagement
MSL training
KOL training
Advocacy development
Peer-to-peer education development and facilitation


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Project Management

Price on request
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Epidemiology, Healthcare, and Post-Authorization Studies

Price on request
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Clinical Trials, Consulting, and Management

Price on request
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Clinical Research

Price on request
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Phase IV Clinical Trials

Price on request
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Jeffrey Trotter

Senior Vice President

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