Exhibitor Directory

2005 S. Easton Rd.
Doylestown, PA 18901
P: 267-757-3000
Bioclinica Research (formerly Compass Research) is part of a premier global site network focused on making your clinical trial a success. Our state-of-art, purpose-built,  Phase 1 facilities are designed to conduct the full range of clinical pharmacology studies from first-in-human (SAD/MAD) studies to complex Ph I/II adaptive trial designs in both healthy volunteers and special patient populations. Our dedicated Phase 1 team brings years of experience to deliver the highest quality data while ensuring safety of study participants. With two locations in Central Florida, a robust and diverse patient database, as well as, expertise in specialized procedures (i.e. cCSF), we bring you more than a site. We bring you a solution.
Booth: 222

4000 Weston Road
Toronto, ON M9L 3A2
P: 416-747-8484 x 254
Bio Pharma Services, Inc. is a client-focused, Contract Research Organization specializing in Phase I/IIa Clinical Trials, Bioequivalence Studies and Bioanalysis, serving pharmaceutical, medical device and biotechnology companies globally.  Our headquarters are located in Toronto, Ontario, Canada, with a 180+ bed, modern clinical facility, which has been inspected by EMA (ANSM & DKMA), UK MHRA, US FDA, Health Canada and ANVISA, and a new 120-bed, US Clinical Facility in Columbia, Missouri.
Booth: 100

One Perserve Pkwy., Ste. 600
Rockville, MD 20852
P: 301-214-6364
As a division of BioTelemetry, Inc. (NASDAQ: BEAT), BioTelemetry Research provides expert Cardiac and Imaging core lab solutions for the advancement of clinical drug development. We offer global operational support for cardiovascular monitoring in all therapeutic areas, and advanced imaging analyses in cardiovascular, oncology, neurology, metabolic, musculoskeletal, and medical device studies. For more information please visit www.gobio.com/research. 
Booth: 509

130 Norfolk St.
Newark, NJ 07103
P: 973-388-2848
Biotrial is your global partner in early development with offices in France, England, Canada, and the United States. We have nearly 30 years of experience providing sponsors with services ranging from Non-Clinical Pharmacology through Phase II-IV Trial Management, to Biostatistics, Data Management, ECG & Imaging Core Lab, and Medical Writing.
Booth: 208/210

9800 Medical Center Dr., Suite C-120
Rockville, MD 20850
Canon BioMedical, Inc. is focused on empowering the biomedical research and healthcare communities by developing, manufacturing and marketing innovative technologies and solutions. The technologies and solutions developed will help enable clinicians and scientists to improve our health and advance science. Canon BioMedical will pursue innovative solutions in line with Canon's Kyosei philosophy. Kyosei is defined as "all people, regardless of race, religion, or culture, harmoniously living and working together into the future." Canon BioMedical will deliver these solutions through the use of existing and emerging Canon technology, as well as strategic partnerships.
Booth: 130

621 Rose St
Lincoln, NE 68502
P: 402-476-2811
Celerion, a leader in early clinical research services, is a global company with over 1,000 employees worldwide. Our unique combination of medical expertise, clinical operations experience and scientific excellence provides our customers with the confidence to make fast, accurate decisions about their drug development path within the clinical research process. Celerion is a full service provider for First-in-Human through clinical Proof-of-Concept studies, including patient dose response studies, cardiovascular safety and clinical pharmacology research supporting product labeling. 
Booth: 406/408

100 Overlook Center, Suite 101
Princeton, NJ  08450
P: 609-716-7900
Certara is a leading decision support technology and consulting organization committed to optimizing drug development and improving health outcomes. Certara’s solutions, which span drug discovery through patient care, use the most scientifically-advanced modeling and simulation technologies and regulatory strategies to increase the probability of regulatory and commercial success. Its clients include hundreds of global biopharmaceutical companies, leading academic institutions, and key regulatory agencies.
Booth: 301/303

401 East Las Olas Blvd., Ste. 130-395
Ft Lauderdale, FL 33301 USA
P: 888-308-7787
ClinicalRSVP is the leading Dual Enrollment Prevention tool for Early Phase clinical trials. Biometric ID technology accurately identifies subjects across Sites and ensures they meet washout criteria prior to enrollment.
Booth: 124

423 W 55th St.
New York, NY 10019
P: 646-215-6400
Clinilabs Drug Development Corporation is a full-service CRO that provides clinical drug development services to industry.  The company provides a broad spectrum of project management, monitoring, data management, biostatistics, and medical writing services.  Clinilabs’ global core laboratory aggregates and processes ECG, EEG, PSG, video, and wearable technology data for multicenter clinical trials.  We operate two clinical research units in the US, offering sponsors 100 beds of phase 1 capability for studies in normal healthy volunteers, patients, and specialty populations.  We are experts in the development of CNS therapeutics.  Learn more at www.clinilabs.com
Booth: 230

210 Carnegie Center
Princeton, NJ 08540
P: 608-210-7592
Covance Inc., the drug development business of Laboratory Corporation of America Holdings (LabCorp) headquartered in Princeton, New Jersey, USA, is the world’s most comprehensive drug development company, dedicated to advancing healthcare and delivering Solutions Made Real®. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, helps our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. Together with our clients, Covance transforms today’s healthcare challenges into tomorrow’s solutions. Information on Covance’s solutions can be obtained through its website at www.covance.com.
Booth: 201

100 Pier 1 Place, Suite 2001
Fort Worth, TX 76102
P: 817-882-6900
CQuentia provides next generation sequencing differentiated by specialized reporting and an integrated analytics engine to optimize actionability of results for care providers and payer. CQuentia solutions utilize hundreds of millions of medical recrods combined with information from peer-reviewed, evidence-based literature. Customers include major healthcare hospitla systems and self-insured employer groups around the US.
Booth: 228

675 Massachusetts Ave.
Cambridge, MA 02139
P: 617-661-2011
Cytel is shaping the future of drug development.  As the world's largest Biometrics CRO, we improve our customers’ chances of success through expert trial design, efficient operational implementation and clinical data management.  Our Quantitative Pharmacology and Pharmacometrics team provides the requisite expertise to support sponsors adopt model-informed approaches to drug development.
Booth 517

300 W. Morgan St., Ste. 800
Durham, NC 27701
P: 919-668-5920
Duke Early Phase Clinical Research partners with the pharmaceutical industry, technology companies, government agencies, foundations, and academic centers to bring clinical validation to innovation. Our academic thought leadership, research unit, specialized patient databases, and clinical and operational expertise accelerates the development of therapies, diagnostics, and medical devices to humans.
Booth: 120/122

Clinical Pharmacology of Miami
550 West 84th Street
Miami, FL  33014
P: 305-817-2900
Evolution Research Group is the largest, independent site company in the US and the leader in early phase specialty population study execution. ERG owns and operates 9 of the leading clinical research units (CRUs) in the US, including CPMI. Clinical Pharmacology of Miami (CPMI) is a 24,000-sq-ft inpatient and outpatient custom-designed clinical pharmacology unit. CPMI offers 120 clinical research beds with for renal, hepatic, FIH, DDI, First to File, FE, PK/PD, SAD/MAD, BA/BE, TQT/QTc, diabetes and sexual dysfunction.
Booth: 325

6-7 Floor, Wing B,
NSL-SEZ Arenda, IDA, Uppal
Telangana 500039 India
P: 91-406-7073333
Excelra Knowledge Solutions is a leading informatics and analytics solutions provider serving the life-science community.
Booth: 307

200 Meadowlands Pkwy.
Secaucus, NJ 07094
P:  877-298-9071
Frontage is a full service CRO which closely collaborates with pharmaceutical and biotech companies to help them bring promising drug candidates to market. With 14 locations in USA and China, Frontage has been assisting clients in their drug development efforts since 2001. Spanning from preclinical through late-stage development, its full service offerings include DMPK, Bioanalytical Services for Small and Large Molecule and Biomarkers, CMC, Early Stage Clinical Services, and Full Biometrics Support.  Booth: 223

4160 Mendenhall Oaks Pkwy., #105
High Point, NC 27265
P: 336-841-0700
High Point Clinical Trials Center has provided comprehensive clinical site services since 2008. Our 42,000 foot facility consists of three unique units for the execution of outpatient and inpatient clinical studies. In addition to healthy normal Phase I studies, we focus on specialty populations such as Diabetes, NASH, Renal Impairment, Respiratory, CNS, Cardiovascular and Nicotine.
Booth: 225

2100 Pennbrook Pkwy.
North Wales, PA 19454 USA
P: 215-606-3000
ICON is a global provider of outsourced drug development services to biopharma, medical device, government, biosimilar and generic organizations. We offer a full range of clinical, consulting and commercial services that range from trial design to full study execution, and from clinical to postmarket commercialization. Our services are supported by in-depth therapeutic and regulatory expertise and market-leading technology and analytics. We are the only full service CRO that offers the knowledge, software and systems for adaptive trials.  With headquarters in Dublin, Ireland, ICON currently operates from 89 locations in 37 countries and has approximately 12,300 employees.
Booth: 202

Nauchny Proezd, 19
Technopark Slava, Moscow 117246
Russian Federation
P: 7-499-645-53-36
InSysBio will be presenting quantitative systems pharmacology (QSP) modeling services and QSP modeling platforms including Immune Response Template, tau and amyloid bet AD platform.
Booth: 106

4820 Emperor Blvd.
Durham, NC 
IQVIA (NYSE:IQV) is a leading global provider of information, innovative technology solutions and contract research services dedicated to using analytics and science to help healthcare stakeholders find better solutions for their patients. Solutions are powered by the IQVIA CORE™, which combines big data, advanced technology, analytics and extensive industry knowledge. Formed through the merger of IMS Health and Quintiles, IQVIA has approximately 55,000 employees worldwide. Learn more at iqvia.com.
Booth 507

1200 Rt 22E, Suite 200
Bridgewater, NJ 08807
P: 908-253-3608
The mission of the International Society of Pharmacometrics (ISoP) is the promotion and advancement of the discipline of pharmacometrics, through Integration, Innovation, and Impact: quantitative integration of multisource data and knowledge of clinical, biomedical, biological, engineering, statistical, and mathematical concepts, resulting in continuous methodological and technological innovation enhancing scientific understanding and knowledge, which in turn has an impact on discovery, research, development, approval, and utilization of new therapies.
Booth: 505

5375 Medpace Way
Cincinnati, OH 45227
P: 513-579-9911
Medpace is a scientifically-driven, global, full-service clinical CRO providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its physician-led, disciplined operating approach that leverages local regulatory and therapeutic expertise.
Booth: 104

2 Tunxis Rd., Ste. 112
Tariffville, CT 06081
P: 860-735-7043
Metrum Research Group is the leading innovator in biomedical modeling and simulation. We have provided strategic decision making with the highest quality of scientific expertise for 100+ companies on over 300 projects. Visit our exhibit booth to learn more about our quantitative approach to drug development and to experience METWORX, our cloud based platform, and mrgsolve, our R package for simulations from ODE-based models. 
Booth: 420

99 Creek St.
Brisbane, Australia
P: 61-7-3105-2887
Model Answers increases the likelihood of successful drug development by applying modeling and advanced analytics to PK and PD data. It specializes in population based analyses to aid dose selection, as well as development of interactive data analysis tools.
Booth: 229

1928 Alcoa Highway, Suite 107
Knoxville, TN 37920
P: 865-305-9100
NOCCR is a privately owned multispecialty clinical research center and a site within the Alliance for Multispecialty Research.   NOCCR-Knoxville is a fully equipped Phase I Unit with 50 beds and 24,500+ sq. ft. of space located within the University of Tennessee Medical Center. This unit excels at FIH, procedurally complex trials and special populations.
Booth: 108

2525 Meridian Pkwy., Ste. 200
Durham, NC 27713
P: 888-615-5111
Nuventra is committed to improving human health through a deep understanding of the sciences that drive drug development. With roots in Clinical Pharmacology, Pharmacokinetics, Pharmacodynamics, Population PK, and Modeling and Simulation our team provides actionable insights, regulatory expertise and strategic guidance to support your team from discovery through late phase development.
Booth: 515

10903 New Hampshire Avenue
Silver Spring, MD 20993
Join Our Team Today!
The Office of Clinical Pharmacology in the office of Translational Sciences, Center for Drug Evaluation and Research, FDA, invites applications from Clinical Pharmacologists with a background in biomedical, biological, pharmaceutical, or pharmacological sciences and strong communication skills. As a clinical pharmacologist at the FDA, you will apply your skills to address unique and precedent setting problems while refining your skills. You will evaluate and advise on protocols for clinical studies and assess the evidence for safety and efficacy from clinical studies submitted in drug and biologics applications from a clinical pharmacology perspective. Our active regulatory research program will allow you to advance your skills and professional development. We have open positions related to small molecules, biologics and biosimilar product review.

Visit the ASCPT Career Center in the Annual Meeting App to learn more.

Booth 229

5055 S. Orange Ave.
Orlando, FL 32809
P: 407-240-7878
Located in the heart of Central Florida, OCRC is a cutting edge independent Phase I – IV custom-built 35,000 sq. ft. research site. Designed specifically for Phase 1 clinical trials, OCRC includes 110 in-house volunteer beds, dual lead digital telemetry, CCTV security system, and cardkey access.
Booth: 204

195 West Street
Waltham, MA 02451
P: 781-487-9900
PAREXEL International, a leading global biopharmaceutical services organization, has been a proven partner of pharmaceutical, biotechnology, and medical device companies for more than 30 years. Together with our customers, we have applied expertise, resources, and technologies in a shared mission to develop life-saving therapies for patients around the world.
Booth: 207

Baltimore, MD
P: 443-685-5800
Pharmaron is a premier R&D service provider supporting the life science industry with diverse and well-established drug R&D service capabilities, from early discovery to clinical development. With operations in China, US and UK staffed by over 5,300 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China. Learn more during our clinical metabolism session on Friday, March 23 at 10:00 am in the Orange Ballroom.  Meet our team at Booth 224.
Booth: 224/226

4130 ParkLake Ave., Ste. 400
Raleigh, NC 27612
P: 919-786-8200
PRA Health Sciences’ early phase professionals live and breathe clinical pharmacology. As the most comprehensive high-end Phase I CRO in the world, PRA Early Development Services provide a unique scientific environment required for complex compound development in both healthy volunteers and special patient populations. Committed to the highest standards of clinical excellence and scientific expertise, we operate state-of-the-art facilities in The Netherlands and North America as well as an innovative patient pharmacology model in Central and Eastern Europe. Our fully harmonized, GLP-compliant laboratories are located close to our clinical units, enabling us to quickly analyze time-critical samples.

Booth: 416/418

1000 Westgate Dr., #149
St Paul, MN 55114
P: 651-641-2914
Prism Research is a 52-bed, early phase research site in the center of Minneapolis/St. Paul metro area. Prism specializes in complex early phase and patient based trials.
Booth 205

9 Nollet Drive
Andover, MA 01810
P:  978-621-9870
qPharmetra, a leader in pharmacometric modeling and clinical pharmacology consulting, helps drug companies increase the odds for clinical trial success by choosing the best dose, designing efficient trials and providing analysis to support positive regulatory reviews. Using cutting-edge pharmacometric techniques, we integrate datasets into mathematical models which drive rational development decisions.
Booth: 231

3 Innovation Way, Suite 240
Newark, DE 19711
P: 302-690-4962
QPS is a GLP/GCP-compliant CRO that supports discovery, preclinical, and clinical drug development. We provide quality services in Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, and Clinical Development to pharmaceutical and biotech clients worldwide. Our regional laboratories, clinical facilities and offices are located in North America, Europe, India and Asia. For more information, visit https://www.qps.com.

Booth: 309

Mere Way
Ruddington, Nottingham NG11 6JS
United Kingdom
P: 44(0)115-974-9000
Quotient Sciences provides formulation development, clinical pharmacology trials, and clinical and commercial manufacturing services to the pharmaceutical and biotech industry. Whatever Phase 1 clinical pharmacology study you require, you can expect rapid study start-up and recruitment through our locations in Jacksonville and Miami (U.S.) and Nottingham (U.K.). 
Booth: 503

777 Old Saw Mill River Rd.
Tarrytown, NY 10591
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions.
Booth: 331

2864 State Route 27, Ste. G
North Brunswick, NJ 08902 USA
P: 888-521-3787
Rudraya is a leading provider of cloud computing, data management and visualizations platform (SONIC), supporting drug discovery at pharmaceutical, biotechnology and and healthcare organizations. Eight out of ten pharma companies are our customers, and are using SONIC to perform cutting-edge genomics, machine learning, modelling, clinical trial simulation, bioinformatics and other computation workflows.
Booth: 305

42505 10th Street West
Lancaster, CA 93534
P: 661-723-7723
Simulations Plus is the premier developer of modeling & simulation solutions supporting drug discovery and development. With subsidiary companies Cognigen Corporation & DILIsym Services, we provide easy-to-use software (including GastroPlus™, ADMET Predictor™, KIWI™, and DILIsym®) and PBPK modeling, pharmacometrics, and systems toxicology/pharmacology consulting services to assist with safety risk assessment and preclinical/clinical development efforts.
Booth: 321

525 S. Silverbrook Drive
West Bend, WI 53095 USA
P: 262-334-6020
Spaulding Clinical Research is a global CRO based in West Bend, Wisconsin providing Phase I – IV drug development services to the biotechnology and pharmaceutical industries. Founded in 2007, Spaulding Clinical operates a 200-bed Clinical Pharmacology Unit, Cardiac Core Laboratory, and provides full Biometrics/Scientific Affairs services.
Booth: 206

3201 Beechleaf Ct.
Raleigh, NC 27604 USA
P: 919-257-6999
Syneos Health (Nasdaq:SYNH) is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies – INC Research and inVentiv Health – we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together, we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to lifeTM visit SyneosHealth.com.
Booth: 221

One Promenade Blvd., Ste. 1101
Fair Lawn, NJ 07410 USA
P: 201-587-0500
TKL Research is a fully integrated network of clinical research centers consisting of two clinical pharmacology units and five outpatient clinics in the NY/NJ metro area. Our comprehensive approach allows us to run your study start to finish. Design. Recruit. Execute. Manage. Report. We are your solution.
Booth: 519

The Hague, DA
P: 31623295637
TNO will exhibit the latest developments on the use of microtracer labelled drugs in clinical pharmacology. Besides the use of microtracers to establish absolute bioavailability, the application of the automated AMS analysis combined with simultaneous direct hrMS/MS for metabolite profiling will be shown. In addition, please visit our booth to discuss possible participation in our joint innovation programs that are under development:- 14C-labelled payloads to facilitate ADC preclinical and clinical studies- pediatric MIST studies for safe dosing and metabolite profiling in children- the TNO fully anaerobic colon metabolite production platform I-screen to establish gut metabolism for low absorbable or enterohepatically circulating drugs- Robot PAL Charlie to increase objective data collection while increasing the fun factor and education level of diseased children in pediatric studies.
Booth: 102

1305 Franklin Ave., #150
Garden City, NY 11530
P: 516-998-7499
Verified Clinical Trials (VCT) is by far and away the largest research subject database registry adopted globally by numerous pharmaceutical companies, CROs and nearly all of the Phase 1 CRUs across the country. Verified Clinical Trials will stop professional research subjects from dual enrollment and is utilized across all phases of clinical research.  Verified Clinical Trials prevents several other significant protocol violations that are critical to a clinical trials success. Verified Clinical Trials is the one and only research database registry selected by NIH/NIDA to protect their trials. Verified Clinical Trials improves research volunteer safety and data quality and reduces liabilities.
Booth: 209

5630 Cerritos Ave.
Cypress, CA 90630 
P: 714-252-0700
WCCT is a multisite, full-service pharmaceutical contract research organization (CRO) of outsourced early drug development and late phase CRO services to the pharmaceutical, biotechnology and medical device industries.
Booth: 227

101 Stations Landing
Medford, MA 02155
P: 781-388-8200
Wiley, a global company, helps people and organizations develop the skills and knowledge they need to succeed. Our online scientific, technical, medical, and scholarly journals, combined with our digital learning, assessment and certification solutions help universities, societies, businesses, governments, and individuals increase the academic and professional impact of their work.
Booth: 404

8609 Cross Park Drive
Austin, TX 78754 USA
P: 512-834-7766
Worldwide Clinical Trials employs more than 1,400 professionals around the world. One of the world’s leading, full-service contract research organizations (CROs), we partner with sponsors in the pharmaceutical and biotechnology industries to deliver fully integrated clinical development and bioanalytical services, extending from first-in-human through phase IV studies. For more information, visit www.worldwide.com.
Booth: 220
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