Supporting Sciences

Explore the comprehensive supporting CRO services provided by Resolian.

Resolian’s dedicated specialists are committed to delivering a wide range of CRO services, either as standalone solutions or as part of a complete drug development package.

Reach out to us directly to learn more about Resolian’s comprehensive supporting CRO services.


Our Supporting Sciences

Statistical PK Analysis

Offering full bioanalytical and PK/TK support for all stages of drug development.

Global Quality

A global team of professionals proficient in GLP, GCP, cGMP, and CSV standards, with expertise in GxP compliant quality systems.

Other Supporting Sciences

Flow Cytometry Sample Processing Packages

The Flow Cytometry team offers sample processing packages with the aim of stabilizing the sample prior to shipping and decreasing variability.

Logistics and Clinical Study Support

Our bioanalysis, logistics, and sample management teams work together to provide an integrated service for global, multi-center clinical studies for our clients.

Data Management

Delivering comprehensive Data Management services using efficient and meticulous processes, coupled with state-of-the-art technologies to ensure your clinical trial data is managed with precision and accuracy. 

Microsampling

Delivering specialized methods and workflows that leverage innovative microsampling technology at the pre-clinical, clinical, and bioanalytical levels.

Document Writing and Publishing

Providing high-quality reports following eCTD guidelines that are customizable to the sponsor’s needs.

 

Project Management

Our Project Management team has extensive expertise in a wide range of study types and therapeutic areas, and will oversee every aspect of your study.

Statistics

Delivering you timely, high-quality statistical services, in accordance with regulatory requirements.

Sample Management

Our sample management kits provide all the materials necessary for accurate, efficient, and safe preparation, collection, and shipment of clinical samples from trial sites to bioanalytical laboratories.

Archiving

Offering GLP-compliant archiving solutions within an HVAC-controlled environment.

Pharmacokinetics – Area Under the Curve Calculations

The area under the concentration vs. time curve is a useful description of exposure of drug following administration. There are different ways in which AUC may be calculated…

Introduction to Pharmacokinetics

An understanding of the characteristics of drug exposure following administration and how it relates to safety and efficacy is critical for progressing drug development (e.g. in decision making for drug candidates…

Pharmacokinetics (PK) Urine Analysis

Whereas blood is collected for analysis at a discrete time point, urine is collected over periods of time known as collection intervals…

Statistical PK Analysis

Offering full bioanalytical and PK/TK support for all stages of drug development.

Global Quality

A global team of professionals proficient in GLP, GCP, cGMP, and CSV standards, with expertise in GxP-compliant quality systems.

Logistics and Clinical Study Support

Our bioanalysis, logistics, and sample management teams work together to provide an integrated service for global, multi-center clinical studies for our clients.

Data Management

Delivering comprehensive Data Management services using efficient and meticulous processes, coupled with state-of-the-art technologies to ensure your clinical trial data is managed with precision and accuracy.

Microsampling

Delivering specialized methods and workflows that leverage innovative microsampling technology at the pre-clinical, clinical, and bioanalytical levels.

Document Writing and Publishing

Providing high-quality reports following eCTD guidelines that are customizable to the sponsor’s needs.

Project Management

Our Project Management team has extensive expertise in a wide range of study types and therapeutic areas, and will oversee every aspect of your study.
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Zhiyang Zhao, Ph.D.

Chief Scientific Officer

Zhiyang Zhao, Ph.D., serves as Chief Scientific Officer (CSO) at Resolian. Dr. Zhao has over 30 years of pharmaceutical industry experience with special focus on drug metabolism and bioanalysis of small and large molecules in drug discovery and development. Dr. Zhao has previously held positions at Pfizer, GlaxoSmithKline, and Amgen. Before joining Resolian in 2015, Dr. Zhao served as Site Director of Preclinical Research at Amgen in Cambridge, Massachusetts, for over a decade. 

Currently, Dr. Zhao serves as an Adjunct Professor at the Eshelman School of Pharmacy of the University of North Carolina at Chapel Hill, North Carolina, and as Editor-in-Chief of Drug Metabolism & Bioanalysis Letters, a journal by Bentham Science, which publishes in all areas of drug metabolism and bioanalysis. Dr. Zhao received his Ph.D. degree in Medicinal Chemistry from Virginia Polytechnic and State University (popularly known as Virginia Tech) in Blacksburg, Virginia. 

Patrick Bennett

Chief Executive Officer

Patrick Bennett has over 35 years of experience in pharmaceutical analysis and laboratory management. Now Chief Business Officer at Resolian, Patrick’s experience includes the roles of Strategic Marketing Director for Pharma with Thermo Fisher Scientific, LabCorp, and Vice President of Strategy and Development with PPD. 

Patrick earned a B.S. degree in Toxicology and a M.S. degree in Pharmacology from the College of Pharmacy and Allied Health at St. John’s University and an M.B.A in International Marketing from the Martin J. Whitman School of Management at Syracuse University.