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QPS Late Stage Clinical Services
 

QPS Late Stage Clinical Services

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At QPS, we realize that in today's late stage drug development space you face many challenges: ...

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
# Biostatistics
# 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
# Allergy
# Alzheimer's Disease / CNS Disorders

For more information, please visit our website: www.qps.com or contact us by e-mail: info@qps-usa.com.

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    QPS Late Stage Clinical Services QPS Late Stage Clinical Services Document Transcript

    • INFLAMMATORY DISEASE ALLERGYCARDIOVASCULAR DISEASE DIABETES F E M A L E H E A LT H PHASE II-IV CLINICAL OVERVIEW ONCOLOGY INFECTIOUS DISEASE QPS Phase II-IV Clinical Overview QPS is your Global Link to all your Phase II - IV Clinical Sourcing Needs
    • Introduction to QPS’ Phase II-IV Clinical Research Services: 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. SITE MONITORING SITE MANAGEMENT PROJECT MANAGEMENTSITE LOGISTICS CLINICAL DRUG RESEARCH PROGRAM MANAGEMENTSITE TRAINING
    • Why should QPS be your first and only choice to conduct your Phase II-IV studies? Professional and Experienced Staff With QPS you get immediate access to its global Clinical Development Teams composed of well-trained Clinical Research Associates, Clinical Research Coordinators, Clinical Project Managers, Regulatory Affairs Staff, Data Managers, Biostatisticians, Clinical Pharmacokineticists, Medical Writers, Quality Control Staff, Safety Reporters and Clinical Research Trainers who are capable of meticulously managing the conduct and taking on the overall responsibility for your clinical trials. As a full-service CRO, QPS can assist you with B A L C R O G L O the entire late stage drug development process: PRECLINICAL Program Management Biostatistics Project Management PK / PD Analysis (includes Pop PK) SiteOManagement & Monitoring BI ANALYTICAL Medical Writing Data Management Temporary Staffing/Flexible Sourcing Solutions CLINICAL DRUG DEVELOPMENTFind out how to Global Flexibility and Capacityachieve your nextdevelopment At QPS, we realize that in today’s late stage drug development space you face many challenges: TRANSLATIONAL MEDICINE QUALmilestone ahead Strict Timelines Insufficient trial populationsof time. Manage increasing amounts of clinical data Budgetary constraints from multiple sources and systemsCall to scheduleyour tour at one With our global presence, QPS is in an excellent position to offer solutions to all of the above needs.of QPS’ worldwide BIOTECHNOLOGY QPS provides high quality data, industry best timelines and a very competitive price. We also havelocations today! access to a large network of investigators for all major types of therapeutic categories.
    • PHARMACEUTICAL INNOVATIONCOST EFFECTIVE BREAKTHROUGHS PERSONALIZED MEDICINE PASSIONATE BENEFIT PATIENTS PRODUCTIVE Customer Focus QPS focuses on the needs of each client and works to make sure that those needs are met. We strive to make certain all studies are recruited fully and completed on time. We also strive to ensure optimal communications so you always have complete visibility into your project’s status and can rest assured that your deadlines will be met and your budgets will not be exceeded. At QPS, we measure our success by your success. Preferred Provider Relationship: Improved Efficiency and Lower Costs Improve the efficiency and effectiveness of your drug development efforts and qualify for volume discounts by embracing QPS as your preferred provider for your specific drug development sourcing needs. You will be assigned a dedicated program manager and enjoy maximum benefit of conducting different types of studies at distinct global sites in order to keep your overall drug development costs as low as possible. 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 Gastrointestinal Disorders Allergy Hemostasis/Angiogenesis Alzheimer’s Disease/CNS Disorders Immunology/Autoimmune Disease/Rheumatoid Anemia Arthritis Asthma/COPD Infectious Disease Bone Disease/Metabolism Inflammatory Diseases/Immune Status/ Cardiovascular Disease Cell Response Diabetes/Obesity/Lipid Metabolism/Carbohydrate Renal Disease Metabolism Thyroid Disorders Female Health Care/Gynecological Endocrinology/ Oncology/Tumors/Neoplasia Reproductive Endocrinology
    • QPS is a reputable and profitable provider of Call to arrange for a tour at one of world-class pharmaceutical development services, possessing unparalleled scientific expertise QPS’ worldwide locations today within our core competencies: DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical, Phase II-IV Clinical and Program Management. NETHERLANDS USA TAIWAN INDIAQPS|Taiwan QPS|CTPS QPS|Qualitix QPS|Bio-Kinetic QPS|HQ QPS|Netherlands QPS|Bioserve
    • Time is of the essence, so contact a member of the QPS Business Development Team today and find out what QPS can do for youNorth America Asia Europe- Wendy Nelson -  eff Moran J - Alex Chang - Jelle Hempenius  +1 508 543 0228  +1 302 690 2163  +886 2 2655 7555  +31 50 304 8000  wendy.nelson@qps.com  jeff.moran@qps.com alex.chang@qps-taiwan.com.tw  jelle.hempenius@qps.com -  erry Gromelski J -  ndrew Nehls A - Manish Kalwani - Fabien du Fraisse  +1 570 451 3015  +1 402 895 2022  +91 40 2377 0873 74  +44 7834 704426  jerry.gromelski@qps.com  andrew.nehls@qps.com manish@bioserve.co.in  fabien.du.fraisse@qps.com -  arina Abanto M - Dave Dehler - Edwin van Vulpen  +1 513 232 4772  +1 540 751 1325  +31 50 304 8000  marina.abanto@qps.com  dave.dehler@qps.com edwin.van.vulpen@qps.com -  im Cunningham J - Stacie Knebel (Phase II-IV Clinical)  +1 402 541 6041  +1 302 635 4341 - Sylvia Demandewicz  jim.cunningham@qps.com  stacie.knebel@qps.com  +32 477 752970 sylvia.demandewicz@qps.com  - Lily Rosa  +1 512 350 2827 HQ BD Office  info@qps.com