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Expedite cardiac safety with a streamlined process With a powerful combination of high performance ECG monitoring and drug development expertise, we bring together operational excellence, medical expertise and global reach to run superior cardiac safety studies and provide biopharma customers with accurate, actionable insights across the product development...
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Marketing in a multichannel world ‘Going digital’ is a global business trend across industries, and pharma has been relatively slow to embrace the technology-fuelled changes of the last decade. At the same time, patients and healthcare professionals increasingly use digital devices for health-related information. At one time, increasing healthcare regulation, declining...
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Educating patients and prescribers can open more doors for your brand and help improve outcomes In the face of healthcare complexity, knowledge is power. The more you educate your stakeholders about your product, the higher your chances of success. Increase drug adherence and compliance through targeted educational programs. Optimize you communication with...
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Our clinical monitoring teams deliver faster, more efficient investigator site support and data oversight Rigorous study-specific CRA preparation. Specialized therapeutic training. On-site in 80 countries, familiar with local customs and regulatory requirements. Streamline clinical monitoring with our Project Coordination Centers We often supplement regular...
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Our Approach Quintiles Advisory Services, the consulting arm of Quintiles, is a different kind of healthcare advisory group – built on a blend of deep industry and therapeutic expertise, strategic problem-solving skills and rich data assets. We bring a broad understanding of end-to-end drug development and healthcare delivery to help firms develop the strategies and...
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From database build to database lock, Quintiles is committed to customizing data management solutions that emphasize transparency, integrity and accountability as much as speed and accuracy. Our clinical data management team produces results that are source-verified, reproducible and cost-efficient. How do we set the standard for delivering data quality? Precision –...
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A purely prospective approach to real-world research can result in long timelines and high costs – and still may not answer all of your questions. Our Outcome® software and Enriched studies integrate the wealth of existing healthcare data now available with primary data from physicians and patients, enriched prospective studies can to greatly increase the amount of...
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Actionable Insights for Better HealthTM Quintiles now provides laboratory services through Q2 Solutions , a Quintiles Quest Joint Venture.  The new organization combines Quintiles’ scale, clinical trial expertise and diverse therapeutic experience with Quest Diagnostics’ operational, scientific and quality excellence, supply-chain network and informatics...
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Go Beyond Regulatory Compliance Ensuring the success of established products goes beyond just meeting requirements. Amidst increasing regulatory complexity and growing stakeholder pressures to reduce costs, while driving revenue, there exists an opportunity to better align regulatory, safety and medical affairs to maximize product value. Enhance Value & Maximize...
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Create lasting, successful patient relationships A strong patient relationship can accelerate go-to-market strategies, compel adherence and encourage support beyond patent expiration. But finding the right patients and disseminating the appropriate information can be difficult without sound connections and strategies. Solidify patient relationships through digital...
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Better processes to help you predict long term efficacy. Quintiles provides comprehensive product development services to deliver precision medicine solutions you can count on. Together with our central laboratory provider, Q2 Solutions, A Quintiles Quest Joint Venture, we offer end-to-end services like biomarker identification, validation, patient screening and more, we...
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Customizing our FSP model on a portfolio, geographic or therapeutic basis, we can: Provide resources – people, processes and systems – across multiple studies in any therapeutic area Help you access new markets, or exit an existing market, while minimizing fixed costs and investments in physical infrastructure Manage and execute a full therapeutic portfolio...
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Uncover the critical evidence of success You’ve spent the millions of dollars to shepherd your product through development and you’ve gained market approval, but there’s more work to be done to increase the likelihood of long-term success. Stakeholders are demanding evidence to support regulatory, reimbursement and prescribing decisions. Staying ahead of competitors will...
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Minimize risk by maximizing insight As drug development becomes increasingly expensive and time-consuming, you need expert insight to make the process more efficient and effective. By knowing the right answers to questions about dosing, patient populations and study design before you invest time and resources, you can determine the best course of action for your product...
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A solid infrastructure allows you to gear up or scale down Whether you’re just entering or phasing out of a market, in one region or in multiple countries, it’s critical to have a strong foundation in place so that you can target the right audiences, focus on appropriate stakeholders and anticipate challenges to ensure patients have access to innovative treatments....
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Adapt to a rapidly changing post-market climate Regulatory agencies increasingly call for more data past market approval. Payers are tightening reimbursement criteria. Without an agile post-marketing strategy, your investment may not reap its full value. Optimize your product’s potential Monitor safety and comply with regulatory commitments, position your product for...
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Quintiles offers a dedicated division focused exclusively on managing these relationships and projects, and a service model designed to meet the unique needs of specialty associations and patient organizations that integrates our expertise in science, medicine, technology and operations. We have worked with 19 patient associations and medical specialty associations since...
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Maximize value while reducing risk Faced with longer timelines, low predictability, escalating costs and increasing regulatory demands, clinical trials are under intense pressure to succeed. Facilitate success with renewed confidence Quintiles combines clinical expertise and technology solutions to manage complex trials efficiently and effectively while helping to plan...
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Your stakeholders, including regulators, payers, patients and providers, are looking beyond market approval; they want to see that your product can deliver proven, tangible value. Through observational research in real-world settings, you gather the real world evidence needed to develop a robust story of safety, effectiveness and quality to clearly detail your product’s...
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Helping you achieve faster, more efficient submissions from start to finishOur comprehensive global expertise can help you confidently interact with Regulatory Authorities around the world, and package and present all the information necessary to allow Regulatory Authorities to make the right decision.  Maximize the commercial value of your productsWe understand the...
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