THANK YOU TO OUR CONFERENCE PARTNERS & EXHIBITORS:
For more information on how to become a Conference Partner and or Exhibitor Opportunities, please contact:
Kelly Murphy, Vice President, Business Development, iiBIG
Tel: 516-442-0176 • Email: info@iibig.com
The Almac Group provides a broad range of services from R&D, biomarker discovery and development, API manufacture, formulation development, clinical trial supply and IXRS® technology (IVRS/IWRS), to commercial-scale manufacture. Almac provides services to more than 600 companies, including all the world leaders in the pharmaceutical and biotech sectors.
The company employs over 3,000 individuals and is headquartered in Craigavon, Northern Ireland. US operations are based in Pennsylvania, North Carolina and California. Almac has now moved into its new North American Headquarters located in Souderton PA.
For more information about the Almac Group, please visit www.almacgroup.com or e-mail info@almacgroup.com
Aspire Independent Review Board provides customized IRB services to meet the unique needs of our clients in all phases of clinical research. We are committed to the highest level of human research protection with an emphasis on flexibility, efficiency and a commitment to customer service.
Aspire IRB is fully accredited by AAHRPP.
At Clinical Resource Network, LLC (CRN), we make clinical trials “patient-centric” by bringing the clinical trial to patients wherever they live, work or play. We have been deploying our international network of in-home nurses since 2003 to increase patient enrollment and retention. Perfecting how we conduct mobile clinical trials is our sole focus. We can execute a “patient-centric” model well because we have highly experienced teams with diverse backgrounds in big Pharma, healthcare, clinical research trials and logistics management. As a result, we deliver evaluable results on time and on budget.
Our mission at
Compounding Solutions is to provide you with customized investigational products for clinical projects of any size. We bring our expertise in formulating dosage forms such as capsules, oral suspensions, tablets, creams and other non-sterile delivery systems. Other services include: acquisition, distribution, repackaging and appropriate labeling. You can count on our flexibility and commitment to bring USP grade products in a timely manner.
Confluent Translations’ mission is to go beyond translation to honest understanding through ongoing dialog with clients to ensure success. We are ISO 9001:2008 certified dedicated to providing quality work in a timely manner. Our name reflects the company’s customer centric philosophy by merging the client and Confluent in a fluid process to obtain a positive outcome. Good translation and cultural training can make everything a company does fall into place internationally. You, your end customers, partners, and employees will appreciate the joy of engaging with people, products and processes in their first language. That’s the most respectful and profitable way to conduct business globally. “Reliable and responsive” are words we hear every day from our clients. Visit
www.confluenttranslations.com or call Nancy Cardone at 412 539 1410 x 101 to make sure your message is clearly delivered.
Forte Research Systems develops clinical and translational research management software. The company’s cloud-based Allegro® Research on Demand product line includes the Allegro CTMS@Site™ system for clinical research sites and disease groups engaged in industry-sponsored clinical trials, and the Allegro CTMS@Network™ system for trial and site management organizations and investigator site networks. Please visit
www.ForteResearch.com
Huron Life Sciences’ Clinical Research Management solutions enhance financial performance, compliance, service levels, and efficiency across the research enterprise for hospitals, academic institutions, and independent research organizations. Our depth of experience, customized approach, and focus on implementation help clients achieve optimum results. Huron’s Click™ Portal software enables institutions to consistently budget, code, and bill trials correctly; improve cash flow through timely sponsor billing and collections
; and negotiate better contracts — all with a single, integrated, configurable
solution.
Meade & Roach, LLP distinguishes itself as a law firm focused on delivering practical solutions for healthcare regulatory compliance needs. Each of our partners has more than a decade of focused, industry-leading experience in this area. The results we have achieved for clients speak for themselves. We not only understand the law, we understand our clients—who range from the country’s largest academic medical centers and hospital systems to stand-alone specialty facilities and physician practice groups.
Medidata Solutions is a leading global provider of SaaS clinical development solutions that enhance the efficiency of customers’ clinical trials. Medidata’s advanced solutions lower the total cost of clinical development by optimizing clinical trials from concept to conclusion: from study and protocol design, trial planning and budgeting, site negotiation, clinical portal, trial management, randomization and trial supply management, clinical data capture and management, safety events capture, medical coding to business analytics. Our customers include biopharmaceutical, medical device and diagnostic companies, academic and government institutions, CROs and other research organizations, encompassing 20 of the top 25 global pharmaceutical companies as well as research organizations of all sizes.
www.mdsol.com
Optum™ is an information and technology-enabled health services business platform serving the broad health marketplace, including care providers, plan sponsors, life sciences companies, and consumers. Its business units—OptumHealth™, OptumInsight™, and OptumRx™—employ more than 30,000 people worldwide who are committed to enabling sustainable health communities.
The people of Optum serve care providers, including 250,000 professionals or groups and 6,200 hospital facilities; more than 270 state and federal government agencies; over 2,000 independent health plans; two of every five FORTUNE 500 employers; 2,200 global life sciences companies; and one in every five U.S. consumers. They help organizations address significant challenges such as improving clinical performance, implementing new models for care delivery and reimbursement, complying with new regulations, and reducing administrative and financial burdens. Optum’s deep understanding of the needs of the multiple participants across the health ecosystem enables it to deliver collaborative solutions that provide the insights and care to help build sustainable health communities.
PCM TRIALS has been providing alternate-site visits since 2008. PCM TRIALS’ approach of directly hiring, training and managing Certified Mobile Research Nurses (CMRNs), rather than subcontracting to local home health agencies, removes significant risk and administration normally associated with clinical trial home-visits. PCM TRIALS’ CMRNs have completed thousands of alternate-site visits across a wide range of therapeutic areas throughout the US. Sponsors, CROs, and Sites see a significant improvement in recruitment and retention, which accelerates trials and reduces costs with the same quality and care as on-site visits. For additional information go to PCMTRIALS.com
Quorum Review is an independent ethics review board that is fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP). Our primary focus is to safeguard the rights and well-being of research participants. We provide sponsors, CROs, institutions, and sites with reliable, responsive service that ensures efficient study start-up and management. For more information, visit www.QuorumReview.com
Schulman Associates IRB has been a leading provider of review services in the US and Canada since 1983. Schulman is AAHRPP accredited and has an unparalleled FDA audit history. Schulman offers a full line of IRB services including expedited protocol review for minimal risk research, informed consent writing, rush review, translations, and real-time eTools for securely submitting documents, tracking the review process and downloading approval documents. In 2011, Schulman acquired Independent IRB, an industry leader in Phase I review service. The transaction allows both organizations to provide one of the most comprehensive suites of review services in the industry.
SNR Denton is a client-focused international legal practice delivering quality and value. We serve clients in key business and financial centers from more than 60 locations in 43 countries, through offices, associate firms and special alliances across the US, the UK, Europe, the Middle East, Russia and the CIS, Asia Pacific and Africa, making us a top 25 legal services provider by lawyers and professionals worldwide.
TrainingCampus.com® is the home of The International Electronic Education Network®. It is both a production area and a market place where members can get discounted products, services and specialties, build educational material to be sold, exchanged or distributed to any arena requiring training, assessments and surveys. We provide the most efficient means of documenting competency for evidence based education.
XaitPorter is a 100% web based software application that allows you to produce proposals, contracts, NDAs, project documentation, and all other critical business documents up to 70% faster. XaitPorter lets several people work on the same document – all at the same time in true collaboration style. Porter automatically takes care of all the formatting (i.e. fonts, styles, figures, numbering, referencing and layout) according to your marketing guidelines, which allows you to focus more time on what matters most, your content. Please stop by our booth in the Exhibitor’s Lounge – at the MAGI Conference.
