2017 Exhibitor Directory
ALTASCIENCES CLINICAL RESEARCH
|ASCPT 2017 Annual Meeting
March 15-18, 2017
(Exhibit Hall open: March 15-17)
Washington Marriott Wardman Park
575 Armand Frappier
Laval, Quebec, Canada H7V 4B3
With facilities in both the U.S. and Canada, Altasciences Clinical Research is one of the largest early phase clinical CROs in North America. They provide early phase clinical development services to biopharmaceutical and generic companies worldwide. Altasciences’ full-service solutions offering includes medical writing, biostatistics, data management and bioanalysis.
BioPharma Services, Inc.
4000 Weston Rd.
Toronto, ON Canada M9L 3A2
Bio Pharma Services, Inc. is a client-focused, regulatory inspected, Contract Research Organization specializing in Bioequivalence studies and Phase I/IIa Clinical Trials, with a total of 250 beds split between our clinical sites in Canada and the USA. We are a physician owned, full-service provider with support services in Regulatory and Scientific Affairs, PK Design and Support, Medical Writing, Data Management/Biostatistics, and Bioanalytical services.
1 Preserve Pkwy Suite 600
Rockville, MD 20852
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. Our cardiac network processes over 2 billion heartbeats a day, while supporting over 20,000 sites and 30,000 devices monthly, and monitoring nearly 600,000 patients and research subjects a year. 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. Our research team is comprised of key opinion leaders, board certified radiologists and cardiologists, sub-specialty scientists, and highly trained technicians. These experts acquire, evaluate, and report high-quality data through an efficient, cloud-based infrastructure. Additionally, we offer integrated spirometry and ECG services in cardio-respiratory clinical trials through an exclusive alliance with Vitalograph. For more information please visit www.gobio.com/research.
130 Norfolk Street
Newark, NJ 07103
Specialized in Early Development, Biotrial provides solutions from in-vivo pharmacology through Early Clinical Development and PoC. Clinical Pharmacology services are offered out of our 150-bed CPU based in France and our brand new 110-bed unit in New Jersey.
9800 Medical Center Drive
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.
621 Rose St.
Lincoln, NE 68502
Celerion, a leader in early clinical research, translates science into medicine. By leveraging over 40 years' expertise, more than 600 beds, and location in North America, Europe and Asia, Celerion delivers a wide range of innovative clinical research solutions.
Booth 10 & 11
100 Overlook Center, Suite 101
Princeton, NJ 08450
Certara is a technology and consulting organization committed to optimizing drug development and improving health outcomes. We use scientifically-advanced modeling and simulation technologies and regulatory strategies to increase the probability of regulatory and commercial success. Our clients include biopharmaceutical companies, academic institutions, and regulatory agencies.
401 E. Las Olas Blvd., Ste. 130-395
Ft. Lauderdale, FL 33301
clinicalRSVP is the leading platform for preventing Dual Enrollment in Early-Phase Clinical Trials. Biometric identification of subjects ensures data integrity and subject safety for Sites and Sponsors.
100 West Gore Street, Suite 202
Orlando, FL 32701
Compass Research, a Bioclinica Research Network site, is one of the most experienced Phase 1 sites in the U.S. Headquartered in Florida, its experienced clinicians are focused on patient safety and quality data. Compass has a total of 83 beds and is recognized for superior cCSF and advanced imaging capabilities.
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 health care challenges into tomorrow’s solutions. Information on Covance's solutions can be obtained through its website at www.covance.com
675 Massachusetts Ave.
Cambridge, MA 02139
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 reliable clinical data management.
At ASCPT 2017, Cytel’s Cecilia Fosser co-chairs the session: “Using Biomarkers to Predict Registration Endpoints: A Look Inside the Crystal Ball". Visit the Cytel booth to meet our QPP experts and learn about our open Pharmacometrics and Data Science positions in the US, UK/Europe and India.
DaVita Clinical Research
825 S. 8th St., Ste. 300
Minneapolis, MN 55404
DaVita Clinical Research has helped nearly 200 client companies with Phase 1-2a clinical trials in healthy normal volunteers and specialty populations. We deliver renal and hepatic trial expertise, 122 beds in two hospital-based facilities with onsite pharmacies, a large specialty population database, and 30+ years of experience.
Duke Clinical Research Institute
300 W Morgan St., Ste. 800
Durham, NC 27701
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.
Evolution Research Group
12 New Providence Road
Watchung, NJ 07069
New to the Evolution Research Group (ERG) network, Clinical Pharmacology of Miami, LLC is a 24,000-square-foot, state-of-the-art, inpatient and outpatient, custom-designed clinical pharmacology unit. CPMI offers 120 clinical research beds with 6 private rooms for healthy volunteer studies and studies requiring special populations. Study experience includes but is not limited to renal, hepatic, DDI, Diabetic, SAD/MAD, BA/BE and cardiac safety.
Excelra Knowledge Solutions Private Limited
6-7 Floor, B-Wing, NSL-SEZ Arena Plot #6, Survey #1
10903 New Hampshire Avenue
Silver Spring, MD 20993
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.
HOW TO APPLY: If you are interested in further information or are considering employment with CDER’s Office of Clinical Pharmacology and will be attending the 2017 ASCPT Annual Meeting, please visit booth #51 or please contact:
CAPT E. Dennis Bashaw, Director, Office of Clinical Pharmacology, Division of Clinical Pharmacology III
Telephone: (301) 796-1502, BB 240-470-5842
700 Pennsylvania Dr.
Exton, PA 19341
Frontage, a full-service CRO with locations in the US and China, supports pharmaceutical clients in their drug development efforts since 2001. Service offerings include analytical testing, product development, DMPK, bioanalysis, clinical, and biometrics. Frontage proudly serves generic, innovator and consumer health companies from IND enabling through late stage clinical projects.
High Point Clinical Trials Center
4160 Mendenhall Oaks Pkwy., Ste. 105
High Point, NC 27265
High Point Clinical Trials Center (HPCTC) has provided comprehensive (Phase I-III) clinical site services over eight years. Our 42,000 ft2 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 Metabolic Diseases, Respiratory, CNS, Cardiovascular and Nicotine-related.
iCardiac Technologies, Inc.
150 Allens Creek Road
Rochester, NY 14618
iCardiac Technologies, Inc. is an industry-leading centralized core laboratory for cardiac safety and respiratory services. Its high precision cardiac safety assessment methodology has set a new standard for precision and accuracy in all phases of clinical trials. The company serves 8 of the top 10 global pharmaceutical companies, as well as numerous small and mid-sized pharma and biotechnology firms. For more information, please visit: www.icardiac.com
|ICON (Bronze Partner)
2100 Pennbrook Pkwy.
North Wales, PA 19454
ICON is a global provider of outsourced drug development services to biopharma, medical device, government, biosimilar and generic organisations. We offer a full range of clinical, consulting and commercial services that range from trial design to full study execution, and from clinical to post-market commercialisation. 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.
3201 Beechleaf Ct., Ste. 600
Raleigh, NC 27604
INC Research (Nasdaq: INCR) is a leading global contract research organization ("CRO") providing the full range of Phase I to Phase IV clinical development services for the biopharmaceutical and medical device industries. Leveraging the breadth of our service offerings and the depth of our therapeutic expertise across multiple patient populations, INC Research connects customers, clinical research sites and patients to accelerate the delivery of new medicines to market. The Company was named “Best Contract Research Organization” in December 2015 by an independent panel for Scrip Intelligence, and ranked “Top CRO to Work With” among large global CROs in the 2015 CenterWatch Global Investigative Site Relationship Survey. INC Research is headquartered in Raleigh, NC, with operations across six continents and experience spanning more than 100 countries.
Institute for Systems Biology Moscow
Nauchny Proezd, 20, Bldg 2
Technopark Slava, Moscow 117246
Immune Response Template is a tool for development of QSP models in immuno-oncology. QSP modeling services.
8 rue de la Renaissance
Join us at the Lixoft booth for presentation of Lixoft products.
Metrum Research Group
2 Tunxis Rd., #112
5375 Medpace Way
Cincinnati, OH 45227
Medpace is a scientifically-driven, global, full-service clinical contract research organization (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, high-science, and disciplined operating approach.
Tariffville, CT 06081
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 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.
New Orleans Center for Clinical Research
2820 Canal St.
New Orleans, LA 70119
865-305-9100 ext 7
NOCCR and VRG are privately owned multispecialty clinical research centers which together have conducted 2000+ clinical trials. Staffing includes full-time MDs, Nurse Practitioner, Nurse/Coordinators, EMTs, nursing assistants, with separate regulatory, data and recruiting departments. 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. VRG and NOCCR New Orleans are focused on conducting later phase studies in a broad array of therapeutic areas.
2525 Meridian Pkwy., Ste. 280
Durham, NC 27713
Nuventra is a leading consulting firm 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.
807 Broadway St. NE, Suite 100
Minneapolis, MN 55413
OneOme’s RightMed® pharmacogenomic test helps providers with evidence-based prescription decisions by combining a patient’s genetic profile and medications in an interactive report that easily integrates into current practices. OneOme’s RightMed test covers cardiovascular disease, cancer, chronic pain, psychiatric conditions, and more. RightMed was co-developed and exclusively licensed from Mayo Clinic.
Orlando Clinical Research Center
5055 S. Orange Ave
Orlando, FL 32809
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. A special treatment/observation area has 12 hospital beds (6 used for onsite Hemodialysis studies). OCRC is specialized in Phase I trials with an emphasis in pharmacokinetic, QTc, and SAD/MAD studies in healthy, hepatic, hemodialysis, renal, hypogonadal, elderly, and postmenopausal populations.
PAREXEL International, a leading global biopharmaceutical services organization, has been a proven partner of pharmaceutical, biotechnology, and medical device companies for 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.
929 North Front St.
Wilmington, NC 28401
PPD's early development services team has the clinical research experience necessary to design, develop and execute programs that allow you to increase efficiencies and accelerate timelines. Our expertise enables us to help you transition data to later stages of research. Conduct your study at one of PPD's clinical research units.
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.
Prism Research, LLC
1000 Westgate Dr., #149
St. Paul, MN 55114
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.
Hellersberg Str. 9
Neuss, Germany 41460
Profil Germany's main business is the performance of early phase clinical trials having a strong focus on obesity, (pre)diabetes , and diabetes complications. One of the core technologies is the hyperinsulinemic euglycemic clamp, used to address action profiles of insulin analogues, beta cell function and insulin sensitivity.
3 Innovation Way
Neward, DE 1971
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 Early & Late Phase Clinical Research to clients worldwide. Our 30+ regional laboratories, clinical facilities and offices are located in North America, Europe, India and Asia. For more information, visit http://www.qps.com.
Richmond Pharmacology Ltd.
St. George's University of London
Cranmer Terrace, Tooting
London SW17 0RE
P: 44 (0)20 8664 5200
2864 Route 27, Ste. G
North Brunswick, NJ 08902
Rudraya is a Scientific Platform and Information Technology Service provider to Pharmaceutical, Biotechnology, and Healthcare organizations with core focus on High Performance Computing, Cloud Computing, Mobile Medical Applications, and Clinical Data Management. Rudraya product range includes: SONIC - Computing Platform, KEEP - Clinical Databases Platform and CPS - Clinical Pharmacology Services Platform.
Simulations Plus, Inc.
42505 10th St. West
Lancaster, CA 93534
GastroPlus™ is the leading PBPK modeling platform for prediction of absorption, DDIs, IVIVCs & population outcomes in humans & animals. DDDPlus™ & MembranePlus™ offer the mechanistic simulations of in vitro dissolution and permeability experiment. And PKPlus™ rapidly generates NCA/compartmental PK modeling reports. These programs are complemented by our PBPK and pharmacometric modeling and simulation services and clinical pharmacology support.
SNBL Clinical Pharmacology Center, Inc.
800 West Baltimore St., 5th Floor
Baltimore, MD 21201
SNBL CPC in Baltimore is a 96 bed CPU specializing in full-service, Phase I/IIa complex clinical pharmacology study execution including integrated FIH, Japanese Bridging, TQT and Patient Recruitment.
525 S. Silverbrook Dr.
West Bend, WI 53095
Spaulding Clinical Research offers a full service Phase I Unit, Biometrics and Phase I-IV Core ECG Laboratory services. Spaulding operates a 200-bed, paperless CPU featuring 96, full 12-lead telemetry beds and an intensive 12-bed unit for First-in-Human/SAD/MAD trials with extensive experience with all types of Phase 1 studies.
101 College Rd. East
Princeton, NJ 08540
Technology solutions and services for early phase clinics to automate and streamline the entire clinic floor.
Anna van Buerenplein 1
2595DA The Hague
A Dutch R&D company, TNO will present its capabilities in the field of microdosing AMS studies showing that these studies may accelerate the clinical development of drugs (small and large molecules). TNO has access to a unique combustion AMS and will demonstrate the differences to a graphitization based AMS.
Verified Clinical Trials
1305 Franklin Ave., #150
Garden City, NY 11530
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.
350 Main St.
Malden, MA 02148
Wiley is a learning business that helps people and organizations develop the skills and knowledge they need to succeed in the areas of research, professional practice and education.
Worldwide Clinical Trials
8609 Cross Park Dr.
Austin, TX 78754
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.
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