An Integrated Approach to Global Clinical Research.
W&P is a global provider of patient-focused Clinical Research Solutions (CRS) to the pharmaceutical, biotechnology, and medical device and diagnostic industries. We are experts, with experience across all study phases and in a diverse and wide range of therapeutic areas. Our shared attributes of innovation, expertise, and passion are at the heart of everything we do.
Our unique global partnering philosophy emphasizes an uncompromising commitment to clinical research and to the highest level of ethical standards and performance in our jobs. We are selective about the projects we engage in because we are devoted to quality and providing our partners with best-in-class service.
W&P deploys an adaptive approach to clinical trial monitoring that directs focus and activities to the areas of greatest need which have the most potential to impact subject safety and data integrity. The key components include:
Our integrated clinical development, biomarker assay, regulatory strategy and commercialization capabilities deliver unique value for CDx programs.
We’ve built well-honed systems, processes, and relationships specific to DCTs that are ready to be applied to your trial—pandemic related or any other. The result is a full portfolio of DCT capabilities to address any challenge your trial might face.
W&P’s Clinical Research Solutions are driven by our higher purpose of delivering solutions to improve patient health and safety. This is more than just a promise, it’s a commitment to keep patients at the center of everything we do.
As a full-service provider, W&P connects your clinical aspirations with our deep scientific and medical expertise, strong therapeutic insights, and unmatched clinical trials experience to help you bring high-quality therapies to market fast – always with the patients’ safety in mind.
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W&P offers end-to-end solutions for all your clinical research needs. W&P can be your ideal partner and guide throughout every step of your clinical trial, from scientific and regulatory support to compliance, pharmacovigilance, site engagement, and data management.
Our expert staff, state-of-the-art facilities, and bespoke services enable you to enhance patient engagement, reduce risk, and gain higher quality data, all towards the ultimate goal of developing better treatments and improving patient outcomes