Elevating our consulting capabilities to accelerate clinical research and bring therapies to market sooner.
YourEncore, a leading provider of drug development and commercialization advisory and consulting services to the biopharmaceutical industry, is becoming part of Advarra. YourEncore, combined with Advarra’s consulting services, provides unparalleled life-sciences consulting expertise worldwide to solve mission-critical challenges and bring life-changing therapies to market sooner. Through our integrated solutions that safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance, Advarra has the talent, tools, and technologies to accelerate the research and drug development journey for our clients.
Advarra Consulting serves biopharmaceutical companies, device manufacturers, academic medical centers, health systems, and institutions in nearly 60 countries. YourEncore exponentially increases the breadth and depth of expertise with industry practitioners who have extensive hands-on experience to provide effective solutions across the product development cycle. The combination of Advarra Consulting and YourEncore creates an agile life sciences advisory and consulting practice with the capability to swiftly mobilize resources and support client engagements worldwide.
Our combined deep bench of expert consultants offers something unique—they come from some of the most respected life sciences companies in the world with an average of over 25 years of industry experience. They’ve been there; they understand the need for innovative, sustainable solutions and they are distinguished in their capability to help clients deliver more valuable assets, implement more efficient organizations, and respond quickly to critical business challenges.
With an insightful knowledge base of more than 12,000 active and 30,000 historical research protocols through our IRB, IBC, and Longboat platforms, our expert teams are empowered with greater decision-making capabilities. What’s more, YourEncore’s center of excellence infrastructure, organized around practices in quality, regulatory and clinical; advances our capabilities to provide outcome-oriented solutions that accelerate innovation, reduce risk, enhance compliance, and drive operational effectiveness and efficiencies.
YourEncore’s quality and compliance subject matter experts help sponsor organizations successfully navigate complex compliance challenges with a broad range of phase-appropriate, fit-for-purpose solutions, including:
- Regulatory inspection readiness and remediation
- Quality management systems
- Audit preparation, execution, and remediation
YourEncore’s seasoned regulatory experts provide the experience-based guidance required to help clients identify the right regulatory pathway, effectively navigate compliance with global regulatory agencies, and ensure a successful regulatory submission. Whether a client needs support across the development process or in preparation for a key milestone, YourEncore is uniquely positioned to provide support from strategic guidance to tactical hands-on execution. Our regulatory solutions and services include:
- Regulatory strategy development
- Regulatory submissions and operations support
- Regulatory policy and intelligence
YourEncore’s experts in clinical provide clients with access to the leading medical and scientific thinking required to advance the development of key assets, as well as the experience-based, strategic thinking essential to drive operational transformation. We help clients innovate how clinical trials are designed and managed with clinical solutions such as:
- Drug and device development consulting
- Clinical trial oversight and remediation
- Pharmacovigilance planning and compliance
- Organization design and optimization
Combining YourEncore with Advarra’s global consulting solutions, market-leading IRB and IBC review services, and technology solutions expands our capabilities toward advancing clinical research: safer, smarter, and faster™.