Clinical

Smarter clinical development. Executed brilliantly.

Increasing costs, growing complexity, longer timelines: these are some of the most daunting clinical research challenges you face today. Quintiles is your ally in this new health environment. We bring the expertise and resources that meet your clinical needs, delivered in a way that addresses your business needs as well.

No matter how complex the challenge, you can be confident that Quintiles will deliver: 

• Smarter approaches to help you reach decisions faster. The expertise of advanced modeling and adaptive clinical trial designs to unmatched global patient access – all delivered through a platform of integrated data analytics.
• Assurance of quality data, on time. No other CRO is seen as better than Quintiles’ data management services in terms of speed of database lock.¹
• More efficient clinical trials. The result of having more experience in Phase II/III trials than anyone – even the top 5 global pharma companies.
• A rewarding working relationship. That’s why more than 90% of investigators want to work with us again.²

¹Third party blind study, 2007.
²Third party blind study, 2009.

Phase I/IIa

In phase one clinical trials, you must quickly assess the potential of your compound to set your strategy for product development.

Phase II/III

Count on specialized expertise to help you determine if your product has blockbuster potential.

Late Phase

Demonstrate product benefits and monitor safety in larger populations with cost-effective study design and execution.

Medical Devices

Trust our medical device veterans to develop the right regulatory, clinical development and post-approval programs.

Emerging Biopharma

Bring your project to market with top biotech specialists and virtual infrastructure.

Bioanalytical Laboratories

Advion Bioanalytical Labs, a Quintiles company, offers industry-leading expertise and resources to help you identify and address complex bioanalytical and drug discovery issues.

Biostatistics

Optimize study design to drive costs down while accelerating timelines and results.

Biosimilars

A holistic biosimilar solution that seamlessly integrates clinical development, multi-country regulatory support, commercialization strategy, quality and compliance to overcome your challenges.

Central Laboratories

Rely on our central laboratory services to deliver on the promise of quality, scientific expertise and proactive customer service according to your trial’s needs.

Clinical Monitoring

Choose a partner with more than 25 years’ experience in conducting clinical trials (more than 1,250 since 2004), from pharmacokinetic studies to megatrials.

Data Management

Improve uniform data quality with flexible, scalable data collection across your trial sites.

ECG

Determine your cardiac safety profile efficiently and effectively at any point in the lifecycle.

Functional Service Provider

Quintiles has a dedicated Global Functional Resourcing team offering a full range of Functional Service Provider solutions.

Lifecycle Safety

Monitor safety over your product’s lifecycle to give you a more precise picture of your product’s performance.

Patient & Investigator Recruitment

Enroll the right patients and identify investigator sites for your trials in accelerated time.

Medical Writing

Turn to our expert team of Medical Writers to keep your development program moving forward

Model-Based Drug Development

Our industry-leading model-based drug development services boost the probability of success in the New Health by enabling you to make critical decisions that optimize resources and returns.

Regulatory

Follow a more efficient path through the regulatory maze guided by our experts.

Quintiles Infosario

Think about what it would be like to immediately track your study’s progress, accessing up-to-date information with only your fingertips. Quintiles Infosario™ delivers this and so much more.

Reporting & Analytics

Leveraging the power of harmonized data to drive actionable clinical insights You expect data quality, but to optimize your compound’s success, we also need data

Data-Driven Processes

Optimize your clinical processes with data-driven work flows To generate real efficiencies for your drug development programs, we need to take advantage of new clinical

Data Archival & Warehousing

We can integrate and archive legacy data from all your studies according to industry standards and regulatory requirements (CDISC / SDTM).

Systems as a Service

Our cloud-based products give you access to best-of-breed commercial platforms and the proprietary technology we use every day to conduct hundreds of clinical trials worldwide.