At QPS, we realize that in today's late stage drug development space you face many challenges:
# Strict Timelines
# Manage Increasing Amounts of Clinical Data from Multiple Sources and Systems
# Insufficient Trial Populations
# Budgetary Constraints
With our global presence, QPS is in an excellent position to offer solutions to all of the above needs. QPS provides high quality data, industry best timelines and a very competitive price. We also have access to a large network of investigators for all major types of therapeutic categories.
With its site management & monitoring teams operating from eight locations on three different continents (Asia/Pacific, USA and Europe), QPS has become a new strong player in the space of late stage clinical research services. Widely recognized for achieving high-quality study data and high patient enrollment rates, QPS' site management & monitoring teams bring years of experience catering to the unique needs of virtual, small, mid-size and large pharmaceutical and biotechnology firms.
As a full-dervice CRO, QPS can assist you with the entire late stage drug development process:
# Program Management
# Project Management
# Site Management & Monitoring
# Data Management
# PK / PD Analysis
# Medical Writing
# Temporary staffing / Flexible Sourcing Solutions
QPS offers a full range of clinical development services for the evaluation of compounds targeted for a wide variety of therapeutic indications including, but not limited to:
# Adrenal / Pituitary Disorders
# Alzheimer's Disease / CNS Disorders
For more information, please visit our website: www.qps.com or contact us by e-mail: firstname.lastname@example.org.