Experience Rapid Study Start-Up & Unmatched Endpoint Quality for Your Respiratory Program
Leverage our ready-to-deploy respiratory team, pre-qualified sites, and existing infrastructure to reduce your study’s start-up period significantly. We can accelerate your first 60-90 days, moving faster than a typical cycle and providing a unique opportunity for rapid deployment of your upcoming respiratory studies.
Our dedicated respiratory team brings extensive experience across a broad spectrum of conditions, ready to tackle both established and emerging indications:
We conduct qualitative interviews with patients and caregivers to gain a deep understanding of their motivations and needs, ensuring that we design our trials with the patient experience as a top priority. Our sponsors consistently report high satisfaction with our responsiveness, attention to detail, and the overall quality of our respiratory delivery teams.
Our commitment to exceptional data quality sets us apart, and we understand the nuances of pulmonary function testing. We ensure superior pulmonary function data through:
Rigorous Training
Guideline Adherence
Strategic Partnership with Clario
Proactive Monitoring
Benefit from our established network of over 100 high-performing sites across North America, Latin America, Europe, and Asia-Pacific. These relationships deliver robust patient recruitment and consistently high-quality data, ensuring the global success of your study.
One patient shared their frustrations with the amount of paperwork needed to participate in the clinical trial process, “Keep it more simplified! For one clinical trial I applied to, they called me back, then sent me 44 pages to review and sign off, then when I got to the study site they gave me the same papers, it took me four hours in my first visit.”
The Cystic Fibrosis Foundation gave Worldwide an “excellent” rating in site relationship and communications. Contact us to talk Cystic Fibrosis.

Franchise Area Lead, Respiratory Medicine
Drew Matheson is Worldwide’s Franchise Area Lead for Respiratory Medicine and has over 25 years experience in clinical trials. He is responsible for the strategy and oversight of our respiratory portfolio and is passionate about bringing new therapies to patients.
Our methodology and delivery puts our partners first in each and every program. We tailor this approach to match the unique medical, scientific, and regulatory needs of everyone we work with.