IVRS Platform-Hosting Services
IVR Concepts is a premier vendor of world-class Interactive Voice Response (IVR) hosted telecom solutions and Interactive Web Response (IWR) applications. Our technology platforms are capable of hosting a multitude of simultaneous applications, any of which can utilize our standard functions, including Prompt Playback, DTMT Digit Capture, Voice Sample Recording, Incoming Call Redirects, Call Blocking, Voice Transcription, Audio Call logging, Credit Card Processing, Custom Database Integration and Extranet Web Site Integration.
Our state of the art facility has all the resources needed to provide impeccable IVR services, both in- and out-bound. These resources include redundant hardware and software, long distance carrier connectivity and text to speech functions. We offer hosted service bureau solutions based on the latest carrier grade, field proven Voxpilot VoiceXML automated speech recognition (ASR) platforms, text to speech (TTS) as well as low-cost , highly efficient touch-tone (DTMF) technologies.
IVR Concepts is a leading provider of hosted IVR and IWR solutions and services that facilitate cost savings and increased efficiency. Our design and customer care teams work closely with our clients to develop applications that automate a wide variety of tasks, eliminating the drawbacks associated with paper data collection methods. and help to avoid non-compliance issues. Our innovative solutions, from reminder, alert and notification messages to the most complex clinical trial processes, can help keep your project on time, prevent budget overruns and ensure protocol compliance.
By providing exceptional customer service, quality and value in our hosted and managed IVR and IWR services, IVR Concepts has earned the trust, confidence and loyalty of clients both domestic and international. We offer organizations of all types and sizes outstanding personal service, platform reliability, advanced technology, industry compliance, large capacity and cost savings.
OmniComm Systems provides customer-driven Internet solutions to pharmaceutical, biotechnology, CROs, research and medical device organizations that conduct life changing clinical trials. OmniComm’s growing base of satisfied clients is a direct result of their commitment to deliver products and services that maximize the value of clinical research investments through the use of innovative and progressive technologies. OmniComm’s solutions offer enhanced interoperability, faster study builds and reduced time to data lock. Currently deployed in over 50 countries, TrialMaster® Electronic Data Capture (EDC) and eClinical Suites have been used in over 3,800 clinical trials around the globe. For more information about OmniComm and their award-winning technologies, please visit www.omnicomm.com.
Criterium Inc. (www.criteriuminc.com) is a full service, global and technology driven contract research organization that offers a unique mix of high-quality, innovative clinical research solutions for the biopharmaceutical, and pharmaceutical, medical device and CRO industries. From thought to finish, Criterium provides timely and accurate clinical trial data and support services at every phase of development allowing customers to make sound and cost effective decisions about their clinical trials. Drug development companies can benefit from Criterium’s expertise, high-value services and products and high-end results. Founded in 1991, Criterium’s services are customized to fit each client’s specific needs, providing a seamless flow of data and information from the investigative site through Criterium back to the sponsor. To learn more about the Criterium Edge, visit the website. Criterium has corporate headquarters in Saratoga Springs, New York with offices in Florida, California, South Africa, India, Netherlands, Israel, Russia and Canada.
Biomedical Statistical Consulting
Quality in Design, Implementation, and Presentation of Biological and Medical Research Studies
Biomedical Statistical Consulting is a contract research organization specializing in the design, implementation, and presentation of clinical trials and other medical research studies since 1986. BSC generates randomization algorithms for clinical trials using block, stratified randomization, and covariate adaptive techniques to support management of balancing sample sizes and controlling the influence of covariates a priori. They have extensive experience in a wide variety of therapeutic area clinical trials conducted to support the regulatory process including 510(k), PMA, and post approval studies. They employ a wide range of statistical tools to studies including frequentist and Bayesian study designs, adaptive study designs, and propensity score methods. An additional benefit is excellent ability to collaborate with Sponsors and their scientific consultants in the design of studies, including hypothesis and outcome measure development; statistical power and sample size analysis; and in the interpretation and presentation of statistical analysis results.
BSC is expert at providing representation for Sponsors at FDA meetings including pre IDE and Panel meetings. They also have substantial experience in ANDA studies for clinical bioequivalence and in scientific research and development including modern classification and prediction technology. The Principal Biostatistician has co-authored over 160 publications in peer-reviewed medical research journals, and is also Adjunct Associate Professor of Statistics in the Medical School of the University of Pennsylvania. BSC staff includes experienced Associate Biostatisticians, Statistical Analysts, Statistical Programmers, and Data Base Managers.
Please visit their website http://www.biomedstat.com and see their interactive consulting resume for more information, including lists of past and current clients, experiences, and areas of expertise.
TCG Supplies – The Coghlan Group
Clinical Trial Material Management
The Coghlan Group provides a full range of services related to clinical trial material management to companies around the world. The company was founded by experienced clinical trial professionals to provide the pharmaceutical research industry with a reliable source for the preparation, packaging/labeling, and randomization of clinical trial material.
As a licensed wholesale pharmaceutical distributor, The Coghlan Group provides FDA-approved products for use in clinical trials. They specialize in the handling of clinical trial material, providing services to include 24/7 “live” patient as well as integration of IVRS/IWRS randomization technologies, and final accountability and destruction of returned drugs. The Coghlan Group strictly adheres to GMP regulations, and is proud to have an extensive list of SOPs.
All details and logistics of shipping clinical trial material around the globe, such as transportation charges, insurance, documentation, duties and taxes are expertly handled. Their secured facility is located 20 minutes from the Austin Bergstrom International Airport and major shippers. Currently, a 40,000 sq. ft. additional facility with six (6) production rooms is well into planning stages.
Over 95% of the Coghlan Group’s business is repeat. Clients value them for their responsiveness, and success at focusing resources for quick resolution of any issues. The Coghlan Group looks forward to working with clients to make their clinical trial a success.