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

Get to clinical results faster with our collaborative approach to strategy, program design and regulatory issues.

Phase II/III

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

Phase IIIb/IV

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.

Biostatistics

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

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.

Patient & Investigator Recruitment

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

Regulatory

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

Medical Writing

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

Lifecycle Safety

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