We’re your full-service CRO solution.
Worldwide’s international infrastructure and dedication to providing responsive, personalized partnerships facilitates your success no matter how complex your drug development program. See what Worldwide’s contract research and bioanalytical lab services can do for you.
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The Worldwide Difference
From start to finish, Worldwide delivers a truly engaged and responsive partnership for your success.
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Making Preclinical and Early Phase Transitions Seamless
Our clinical pharmacology unit and integrated bioanalytical laboratory are located near each other to allow for rapid sample processing and data generation.
Making Preclinical and Early Phase Transitions Seamless
Biotech firms with a molecule ripe for study can benefit from a strategic research partner sooner rather than later. Our clinical pharmacology unit and integrated bioanalytical laboratory are located near each other to allow for rapid sample processing and data generation. Each facility offers leading-edge technologies, advanced clinical and analytical services, and extremely high quality. From protocol concepting and scientific consulting to IND support, and from data and project management to multi-site, first-in-human pharmacokinetic and clinical monitoring, our preclinical and early-phase services take the
Sherilyn Adcock, PhD., RPh.
Chief Scientific Officer,
Early Phase Development
Lona Sheeran
Senior Vice President,
Head of Clinical Pharmacology Services
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Full-Service Clinical Trial Support
Our team is constantly on the lookout for efficiencies and opportunities to make your data, budget, and efforts go further through strategic planning and proactive communication with regulatory and program stakeholders.
Full-Service Clinical Trial Support
Once clinical research is underway, you can rely on our broad team of experts to diligently manage your drug development program. Our team is constantly on the lookout for efficiencies and opportunities to make your data, budget, and efforts go further through strategic planning and proactive communication with regulatory and program stakeholders. Advanced biostatistics support, our global network, access to our leadership, and intelligent, adaptive approaches to challenges provide you with the best partner to navigate the difficult road toward approval.
Michael Murphy, MD., PhD.
Chief Medical and Scientific Officer
Jeffrey Zucker
Senior Vice President, Global Clinical Operations, Site Management & Trial Optimization
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Regulatory, Commercialization, and Beyond
We understand that the end goal doesn’t exist in a vacuum; it involves hitting strategic targets throughout the program. Our inhouse teams are diverse in knowledge and background, with the expertise needed to partner with you at every step of your program.
Regulatory, Commercialization, and Beyond
The end goal for each client may be different. Whatever your strategy – finding a buyer, partnering with big pharma, or marketing the drug yourself – Worldwide can help you get there. That’s because we understand that the end goal doesn’t exist in a vacuum. It involves hitting lots of strategic targets along the way. Through early and ongoing discussions with regulatory bodies, and strategic planning throughout the entire development program, we help ensure our clients and their molecules are prepared for the rigorous review process.
And our services don’t end at a successful product launch. We offer continuing support through real-world evidence gathering, patient-reported outcomes studies, health economic and outcomes research, economic dossiers and modeling, safety surveillance, literature reviews, and more.
Aman Khera
Global Head of Regulatory Strategy
Jeff Trotter, MBA.
Senior Vice President, Scientific Solutions, Real World Evidence
No matter the challenge, we can help.
Developing an integrated, big-picture roadmap for your molecule .
Worldwide offers full-service assistance, from mid-preclinical phases to commercialization and beyond. By working with a partner skilled in the nitty-gritty details and infrastructure of early development and late phase trials, regulatory requirements, and market access, you get a customized, strategic roadmap to get you where you want to go.
Adapting to changes without losing sight of – or progress toward – the end goal.
When the development process hits inevitable bumps in the road, having the right CRO partner makes all the difference. Knowing how to navigate new hurdles, re-envision the development process, and strategically align with regulatory and industry requirements can help your molecule maximize its success premarket so that it’s ready for an impactful launch. A nimble, responsive, experienced CRO can help you avoid major pitfalls and adjust intelligently to any challenge.
Maximizing ROI and minimizing risk through planned and timed steps.
There’s a lot that goes into drug development. Having a single partner you can rely on – who knows your drug and company strategy inside and out – means each part of your journey is done with care and forethought about the impact on both the present and future of your program. It also results in fewer interruptions and delays, a more predictable development and regulatory review process, tighter budget control, and a more responsive, in-depth relationship with your CRO.