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Medical Science Liaisons facilitate and speed market approval These highly experienced Pharm.D., M.D., D.D. or Ph.D. professionals build, create and maintain relationships between biopharma, clinicians and health authorities to facilitate and speed market approval. We can also supply certified nurses in specific therapeutic areas such as oncology. We are agile enough to...
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Biopharma companies have an increasing dependence on in-licensing and acquisitions to grow their portfolios and bridge their pipeline gaps. To increase their probability of success, Quintiles offers a due diligence solution that provides an objective data supported evaluation process provided by our flexible and adaptable team of experts that have vast clinical and...
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As the demands of clinical development change, being nimble and adaptable becomes more critical. Meeting the evolving needs of multiple stakeholders ultimately determine the probability of success. And new agile development models are required to meet customer needs and increasing competitive intensity. Innovative technologies allow pharma companies to explore and...
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A global environment governed by rigorous regulatory and safety requirements brings complexity. And having to understand and manage local regulatory requirements presents a significant burden. Few companies are able to fully maintain a current global regulatory intelligence database, and few have the infrastructure to handle rapid increases in safety-related activities...
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Mature products – products that are close to patent expiry or have recently lost their exclusivity – are often neglected or under-promoted. Innovative companies need to focus on developing a “string of pearls” to provide new, but smaller revenue streams to replace aging blockbusters and so often cannot sufficiently resource mature products. Biopharma companies have...
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  The changing healthcare landscape poses significant challenges to the traditional, segmented biopharma product development model. As the industry increasingly looks for more integration and a greater depth of evidence, market insights alone are not enough. And when it comes to market research, insights alone aren’t enough. You need research combined with strategy – a...
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As outsourcing within biopharma companies has increased, partnerships have become more strategic with companies looking to maximize asset value by increasing speed to patient and optimizing productivity and efficiency of clinical development. There is a clear trend toward closer relationships with fewer CROs and longer contracts. However, historical challenges typical...
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The changing healthcare landscape poses significant challenges to the traditional, segmented biopharmaceutical product development model. Asset development has become increasingly complex as companies trying to optimize their ROI work to meet the value objectives and evidence needs of different stakeholders in order to optimize the return on their assets. Addressing...
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Pharmaceutical, biotechnology and medical device companies have been presented with extraordinary regulatory and quality compliance challenges, as a result of consolidation, restructuring and economic uncertainty. Without the right attention, these challenges can weaken quality systems and processes, erode domain and critical thinking expertise, and cause core quality...
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Healthcare systems are transforming from volume to value to outcomes. This shift fundamentally changes the way that biopharmaceutical companies approach drug development. The Quintiles Value & Outcomes Strategy Solution generates evidence to help define a product’s clinical, economic and humanistic profile. These services are tailored to individual stakeholder’s needs...
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Product launches are critical in biopharma companies’ long term success, yet they are increasingly challenged in today’s environment. Biopharma companies are struggling to find solutions to these challenges (rising costs and restrictive market access) and in most cases, are failing to meet sales expectations. Changes in healthcare systems (increased focus on value and...
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The success of a clinical development program depends on the proper documentation of research plans and results. Quintiles offers a range of flexible Medical Writing and Document Publishing solutions to support various clinical study documentation needs. Medical Writing Our team of more than 70 writers have experience working in a broad range of indications and...
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Relevant and accurate information is key to better insight into your stakeholder needs Product and disease registries are vital tools, but collecting and harnessing meaningful information requires a special approach. Obtaining results that accurately reflect real-world situations takes understanding and experience. Transforming data into resources that inform better...
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Help regulatory authorities make the right decision You know your product’s story and have confidence in the data. And you have no doubt the product will make a difference in the lives of patients worldwide. But you need to ensure that regulatory officials have all the information they need to come to the same conclusion, even after a lengthy and complex registration...
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Build and strengthen communications Recruitment is a complex process involving not only patients but physicians, sponsors, trials professionals and research staff. Hindered by tight timelines and often fragmented communications, recruitment rates can be disappointingly low. A partner who can facilitate strong relationships with investigators and sites and quickly connect...
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An integrated clinical solution Escalating costs, unexpected timeline extensions and low success rates are common in clinical development. To combat these challenges, you need an end-to-end solution to transform strategies and optimize processes for increased efficiency, greater predictability and better outcomes. Full-spectrum strategies and insights With Quintiles,...
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In partnership with Quintiles, the American Heart Association (AHA) created four premier Get With The Guidelines® programs designed to help hospitals ensure continuous quality improvement in patient care for heart failure, stroke, resuscitation and atrial fibrillation. Get With The Guidelines® focuses on care team protocols to ensure that patients are treated and...
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Small Molecule, Biologic and Biosimilar Expertise Our scientists have extensive bioanalytical method development and LC/MS/MS expertise to meet study needs. Highly trained staff utilizes leading-edge technology including AB SCIEX™ mass spectrometers and state-of-the-art extraction techniques. Clients experience superior service and results during routine as well as...
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Ligand Binding Assays ELISA Assays Mesoscale (MSD) Electrochemiluminescence (ECL) Luminex Neutralization Antibody Assays Cell-based Assays Additional Assays Macromolecule Pharmacokinetic Assays Immunogenicity Testing Assays Biomarker Assays Technical Transfer for Developed Assays Novel Assay Development Assay Validation ...
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New opportunities for biomarker integration The use of biomarkers in clinical development programs is a growing requirement for many disease areas.  With this, new opportunities to integrate biomarkers into your clinical development plan are arising including: Identifying the right biomarker for a mechanism of action or specific disease indication Choosing the...
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