Medidata Solutions (http://www.mdsol.com) is a leading global provider of SaaS-based clinical development solutions that enhance the efficiency of customers’ clinical trials. For over 10 years, Medidata has consistently brought next-generation innovation to the life science industry to lower the total cost of clinical development through informed trial planning and management, optimized clinical processes and platform interoperability. Medidata’s advanced solutions address key functions throughout the clinical development process including protocol development (Medidata Designer®), trial planning and management (Medidata Grants Manager®, Medidata CRO Contractor®), user and learning management (iMedidata™), randomization and trial supply management (Medidata Balance™), monitoring (Medidata Rave Monitor, Medidata Rave Targeted SDV), Serious Adverse Events capture (Medidata Rave Safety Gateway) and clinical data capture, management and reporting (Medidata Rave®). Our diverse customer base spans biopharmaceutical companies, medical device and diagnostic companies, academic and government institutions, CROs and other research organizations, and includes more than 20 of the top 25 global pharmaceutical companies as well as organizations of all sizes developing life-enhancing medical treatments and diagnostics.
DZS Software is a SAS reseller! Come to us for savings on SAS licensing
As of March 1, 2007, DZS Software is now a reseller of SAS Software. As a Silver Alliance Partner, DZS enjoys a close collaborative relationship with SAS resulting in superior software. As a participant in the new SAS channel program DZS is able to tailor SAS licensing to each customer's unique ClinPlus requirements often resulting in lower overall costs. This program answers the call for a reliable resource with a comprehensive offering to help grow their business and maximize their clinical trials data management and analysis software investment.
Expertise in Validating ClinPlus® Software!
META Solutions offers validation consulting services to help clients assure that their computerized systems and procedures meet U.S. Food and Drug Administration (FDA) requirements. The META Solutions' ClinPlus® Validation Suite was developed to help clients identify priorities and risks and guide these required activities to ensure their ClinPlus® computerized system is appropriately validated and remains validated. For more information, visit the META Solutions website.
We are a Microsoft ISV partner!
Microsoft offers software options that provide industry with the building blocks to create and distribute software and hardware solutions to other businesses. For more information, visit the Microsoft website.
Citrix for ClinPlus® Software!
Citrix Systems, Inc. is the global leader in access infrastructure solutions and the most trusted name in secure access for enterprises and individuals. Their access software, services, and appliances makes every organization an on-demand enterprise where information is securely, easily, and instantly accessible from anywhere, using any device.
ClinPlus® Joins IBM's ISV Advantage Initiative!
IBM is the world's largest information technology company and a leading provider of e-business solutions. The ISV Advantage Initiative provides independent software vendors (ISVs) the opportunity to offer their customers flexible and secure solutions for their applications by using IBM's industry-optimized infrastructure software.
DZS is a UMC partner!
UMC offer tailor-made lexicon products and analytical services for the international community of pharma and biotech companies, CROs and software developers. Primary products are: WHO Drug Dictionary (WHO-DD) The world's most comprehensive dictionary of medicinal product information. Vigibase Services Leading-edge medicinal database analysis. Early risk forecast using advanced Neural Network intelligence. Flexible querying of WHO's ADR database. WHO-ART Flexible querying, retrieval and tabulation of international ADR data. WHO-ART terminology, highly refined terminology for coding clinical information.
WebtrialZ for ClinPlus® Software!
APT Information Technology Consultants is a specialized infrastructure services company that developed WebtrialZ. WebtrialZ combines all of the server hardware, software, database technology, network services, consulting and support necessary to deploy your validated pharmaceutical application directly to the internet, privately to your company, or both - in one complete package of services. WebtrialZ enables your precious data management resources to focus on their specialty - data management - leaving the chore of system and database management, security, and network operations to us.
European Distributor(except UK) for ClinPlus® Software!
NorthWise Services Ltd. offers a range of services, including data management, statistics, and medical writing, to the pharmaceutical industry, and other services through strategic partnerships.
UK (United Kingdom) Distributor for ClinPlus® Software!
Amadeus Software Ltd.'s provides SAS® Programming and SAS® Consultancy with an excellent return on investment for existing and new Business Intelligence Solutions.
The Society for Clinical Data Management, Inc., (SCDM) is a non-profit professional society founded to advance the discipline of clinical data management. The binding interest of all members is quality clinical data management practices.
The Society of Clinical Research Associates, Inc. is a non-profit, professional organization dedicated to the continuing education and development of clinical research professionals.
PharmaSUG is a forum for the exchange of information and the promotion of new ideas concerning the use of SAS software as it relates to quantitative health sciences including epidemiology, health economics, health management, outcomes research, biostatistics, clinical research and the pharmaceutical industry.
MDMA's mission is to promote public health and improve patient care through the advocacy of innovative, research-driven medical device technology.
ACRP is a global association comprised of more than 20,000 individuals in over 60 countries dedicated to clinical research and development.
The global source of news, directories, proprietary market research, and analysis for clinical trials professionals and patients.
The American Society for Microbiology is the oldest and largest single life science membership organization in the world. Membership has grown from 59 scientists in 1899 to more than 43,000 members today, with more than one third located outside the United States. The members represent 26 disciplines of microbiological specialization plus a division for microbiology educators.
The Regulatory Affairs Professionals Society (RAPS) is the leading worldwide member organization devoted to the health product regulatory profession. With more than 12,000 individual members from industry, government, research, clinical and academic organizations in more than 50 countries, RAPS develops professional standards for knowledge, competency and ethics and is the leading source of information on the scope of practice of regulatory professionals and their critical roles in the health sector. Founded in 1976, RAPS advances learning and fosters knowledge exchange in regulatory, scientific, business, legal and other areas essential to effective product development and regulation. (See more on RAPS history.) RAPS administers the only recognized credential for the profession-the Regulatory Affairs Certification (RAC).
AMWA's mission is to promote excellence in medical communication. Through an extensive educational program, various publications, and unparalleled opportunities for networking, AMWA encourages and enables its members to extend their professional expertise.
BIO is the world's largest biotechnology organization, providing advocacy, business development and communications services for more than 1,200 members worldwide. Our mission is to be the champion of biotechnology and the advocate for our member organizations-both large and small.
The Board of Editors in the Life Sciences (BELS) was founded in 1991 to evaluate the proficiency of manuscript editors in the life sciences and to award credentials similar to those obtainable in other professions.
ISPE, the International Society for Pharmaceutical Engineering, is the world's largest not-for-profit association dedicated to educating and advancing pharmaceutical manufacturing professionals and their industry. Founded in 1980, today ISPE serves 25,000 members in 90 countries.
The global federation of national associations representing 2 million pharmacists and pharmaceutical scientists around the world.
The American Association of Pharmaceutical Scientists, a professional, scientific society of more than 12,000 members employed in academia, industry, government and other research institutes worldwide. Founded in 1986, AAPS provides a dynamic international forum for the exchange of knowledge among scientists to enhance their contributions to public health. AAPS offers timely scientific programs, on-going education, information resources, opportunities for networking, and professional development.
The American Statistical Association (ASA), a scientific and educational society founded in Boston in 1839, is the second-oldest, continuously operating professional society in the United States. For 170 years, the ASA has provided its members and the public with up-to-date, useful information about statistics. The ASA has a proud tradition of service to statisticians, quantitative scientists, and users of statistics across a wealth of academic areas and applications.
Founded in 1999, Capterra is the online marketplace dedicated to connecting buyers and sellers of enterprise software. Capterra has helped millions of people select the right software for their organizations, while providing the ideal online channel for software vendors to reach active buyers. As the online marketplace for the enterprise software industry, Capterra helps organizations make better software purchase decisions, while helping software vendors reduce the cost of reaching IT buyers.