With MDS Pharma Services as your partner, you are working with the most experienced CRO in the world. With five clinical facilities and more than 1100 beds, no other research organization equals our knowledge, our capacity, or our commitment to your success. MDS Pharma Services' capabilities and expertise in clinical pharmacology are simply unmatched.

Yet beyond our extensive expertise, our time-proven processes, and our highly trained staff, we offer another advantage others cannot—the commitment to intelligently apply our collective resources to ensure that your study progresses quickly, seamlessly, and successfully.

We have helped establish the global standards by which all clinical studies are conducted. Now the strength of that experience is intelligently applied to deliver the data you require to support crucial decisions.

We offer a full array of services in both Phase I and Phase IIa studies, including:

• Clinical pharmacology
• Clinical research (IIa)
• Clinical laboratory
• Data management
• Statistical services
• PK/PD analysis

With these services and decades of experience, we can support you at every step along your study's path to help you make the critical decisions you need to—quickly.

Phase I
No other CRO comes close to matching the collective experience and resources of MDS Pharma Services in early clinical research. In addition, you have our commitment to apply our resources intelligently at all levels of planning to best meet your drug development needs. Efficient, accurate, cost-effective solutions—these are the results of intelligence applied to your study—only from MDS Pharma Services.

Bioequivalence Studies
For your next bioequivalence program, MDS Pharma Services will help get your product to market faster. We offer global clinical capacity, on-time recruitment capabilities, proactive study design and assay development programs—all of which mean faster study start-up for you.

Pharmacokinetics / Pharmacodynamics
MDS Pharma Services provides comprehensive data management, statistical and pharmacokinetic services, from protocol development and case report form design to regulatory submission assistance.

Early Clinical Research

Phase I-IIa

Bioequivalence Studies

PK/PD

Study Design and Protocol Development

Data Management

Statistical Analysis

PK/PD Analysis

Medical Writing and Reporting

Modeling and Simulation

Consultation

Webinars

First-In-Human Studies