In The News
Medidata Solutions' products are creating a buzz in the scientific and IT communities. Here are just a few stories highlighting recent successes.2013
The CNBC and Yahoo! Finance “Big Data Download” series features Medidata president Glen de Vries discussing how big data can help make the drug development process more efficient, cutting trial timelines and costs and ultimately creating better outcomes for patients.
Read
Medidata CEO Tarek Sherif is included in Chief Executive magazine's list of “Eight State Advocate CEOs,” part of its “2013 Best and Worst States for Business” series, and is highlighted for his role promoting other tech-entrepreneurship in NYC by mentoring CEOs of start-ups and supporting local university programs that foster business innovators.
Read
Speaking with TheStreet.com, Medidata CEO Tarek Sherif discusses how the Medidata Clinical Cloud is helping life science organizations bring better drugs to market, faster and with less cost and risk.
View
Medidata president Glen de Vries is named one of the “20 Innovators Changing the Face of the Clinical Trials Industry” in the April issue of The CenterWatch Monthly for pushing the envelope of cloud-based technologies in clinical development.
Read
The April issue of ACRP's The Monitor features Medidata senior product director Stephen Young as he discusses his career evolution from aerospace to the world of clinical development, and how his passion for analytics and data-driven development led him to this change.
Read
A recent FierceBiotechIT article highlights the roles of Medidata Solutions and Digital Infuzion in a groundbreaking observational study by Inova Translational Medicine Institute, which will examine the correlation between a child’s genetic profile, their development and their long-term health. Together, Medidata and Digital Infuzion will deliver a web-based portal and cloud technology that will act as a repository for patient data and will enable the review of study progress and access to surveys and study information.
Read
This FierceBiotechIT article offers insights from a recent webinar session, “Drugmakers go mobile,” moderated by executive editor Ryan McBride. Medidata Solutions president Glen de Vries presented—along with industry experts from Genentech, Dotmatics and Kony Solutions—on how pharma companies are embracing digital health and the use of mobile.
Read
Veeva Systems' blog Veeva Voice features a post by Medidata director of product marketing Jay Smith on the challenge and potential of cloud-based electronic trial master files (eTMF) and how they can revolutionize the management of clinical trials.
Read
In this eCliniqua article, Medidata product manager Igor Altman discusses the key issues for ensuring success when adopting new processes for study design optimization.
Read
In a recent Software Magazine article on the evolving healthcare industry and how it opens doors for new and improved IT solutions, Medidata president Glen de Vries discusses the meaningful use of electronic health record (EHR)/electronic medical record (EMR) systems and how Medidata’s cloud-based platform helps to reduce cost, reduce risk, and enhance efficiency in all stages of the clinical trial process.
Read
FierceBiotech highlights Purdue Pharma's recent multiyear deal with Medidata Solutions, broadening its already wide use of Medidata’s cloud-based solutions. The adoption will further enhance Purdue's clinical trials for pain medication.
Read
In a recent PharmaVOICE article on the future of the cloud in clinical research, Medidata president Glen de Vries shares his insight on how the cloud era will go beyond convenience and speed by bringing increased productivity across the trial team.
Read
In the January/February issue of Journal for Clinical Studies, Medidata’s vice president of trial planning solutions Frank Cattie discusses the three key variables of overall study cost—protocol complexity, geography and phase and indication—as well as ways for sponsors to control these variables, reduce study risk and increase performance predictability.
Read
Applied Clinical Trials online in January features a Medidata Insights benchmark for source document verification (SDV) coverage. Part of a monthly series highlighting industry metrics, this edition focuses on how FDA guidance on risk-based monitoring has impacted SDV coverage across the industry.
Read
2012
Forbes' Matthew Herper highlights the Forbes Healthcare Summit panel discussion on big data, led by Medidata president Glen de Vries. The feature includes video clips from the event in which Glen discusses how technology and the copious amount of data collected can help improve productivity in life sciences and health care as a whole.
Read
In a recent article posted by Journal for Clinical Studies, vice president of clinical solutions Jeffrey Handen discusses the need to adopt a more responsive, adaptive and agile model for clinical trials—as well as the evolution of the tools and methodologies needed to efficiently support this model—in order to reduce the product development life-cycle in drug development.
Read
In a Fast Company feature profiling managers who are navigating big job transitions, Medidata’s human resources project manager Naimisha Chanumolu discusses the challenges of going from a software engineer working alone to a project manager overseeing a team of 25.
Read
In a recent PharmaVOICE article on how the optimization of certain processes in clinical development is vital for the timely and efficient approval of new treatments, director of product management Michelle Marlborough assesses the impact of unnecessary procedures in a protocol, referencing the recent Medidata-sponsored study by the Tufts Center for the Study of Drug Development.
Read
In the November/December issue of PharmaVOICE, President Glen de Vries—along with other thought leaders from all sectors of the industry—offers his viewpoint on the most important business objectives for life sciences, both into the new year and beyond.
Read
In the November/December issue of PharmaVOICE, vice president of trial planning solutions Frank Cattie discusses the importance of considering protocol site work effort (SWE) in determining payment levels in order to avoid extended site negotiations, delayed start-ups and low site satisfaction.
Read
Applied Clinical Trials online in November features Medidata Insights™ benchmarks for data entry times and data correction rates. Part of a monthly series highlighting industry metrics, this edition focuses on the impact of delays in entering data on the relative quality of the data being entered.
Read
In InformationWeek’s 2012 State of IT Staffing Survey—which examines the evolving role of application delivery specialists and career prospects for people with these skills—senior vice president of applications and platform Vikram Shah comments on how the cloud has changed how clinical trial software is developed, deployed and delivered.
Read
In this issue of Journal for Clinical Studies, director of CRO partnerships Julian de Bres shares his vision on how clinical research organizations (CROs) and their growing relationships with sponsors drive drug development and leverage clinical trial technology to optimize their studies.
Read
In the fall issue of SCDM Data Basics, vice president of implementation services Marco van Doeveren discusses the power and breadth of cloud computing to better manage the increasing volume and complexity of clinical data.
Read
FierceBiotechIT highlights 15 mobile apps in life sciences for 2012, including Medidata Patient Cloud™, a new app built to simplify patient data collection on iOS® devices such as the iPhone® and iPad®.
Read
Applied Clinical Trials online in October features a Medidata Insights™ benchmark for EDC autoquery rates. Part of a monthly series highlighting industry metrics, this edition focuses on the relationship between EDC autoquery rates and site quality.
Read
In a recent Scrip Clinical Research article, director of product management Michelle Marlborough and senior manager of product marketing Joshua Pines discuss the increase in clinical trial complexity, concentrating on non-core procedures in protocol development and what organizations can do to minimize them.
Read
FierceBiotech’s Ryan McBride features Medidata as a key player driving the advancement of clinical trials in Japan as vaccine maker KAKETSUKEN becomes the first Japanese pharma company to implement Medidata’s cloud-based solutions for randomization, trial supply management, electronic data capture and clinical data management.
Read
In the September issue of Journal for Clinical Studies, senior manager of product marketing Sean Cheng analyzes current trends in source document verification (SDV), highlighting obstacles to overcome and pointing to the need for further awareness and adoption of risk-based practices.
Read
A recent eCliniqua article highlights how Medidata’s deployment of Opscode Hosted Chef enables automated IT infrastructure in the cloud across clinical development processes, delivering new solutions securely in real-time.
Read
Bio-IT World’s eCliniqua reports on the launch of new research from U.S. Department of Health and Human Services (HHS), which uses Medidata’s comprehensive trial cost database products to identify factors that delay or derail clinical studies and help assess policies that encourage and enable more streamlined and efficient trials.
Read
Medidata’s vice president of information security and privacy Glenn Watt is featured in a recent Crain’s New York Business article on the popularity of hackathons as cost-effective tools to identify problems, attract talent and unleash innovation at NYC businesses. Glenn provides insight into how Medidata leverages hackathons to hack into their own code and expose bugs, helping to improve the security of its solutions for customers.
Read
Applied Clinical Trials online in September features a Medidata Insights™ benchmark for query rates. Part of a monthly series highlighting industry metrics, this edition focuses on the rate at which clinical data is queried—whether by data managers, clinical (site) monitors, medical monitors or EDC systems (autoqueries)—which can be used to estimate the quality of clinical sites.
Read
In a Fast Company article on key steps to building a successful business, Medidata President Glen de Vries shares about Medidata's history and growth path to becoming the forward-thinking technology company it is today.
Read
Medidata's vice president of implementation services Marco van Doeveren has been named one of the most influential people in clinical technology in the PharmaVOICE 100. Marco is awarded for his efforts behind Medidata's success helping mid-market organizations to reap the full benefits of advanced technology in clinical trials.
Read
In an article summarizing themes from recent tech company earnings announcements, The Street names cloud, storage and security as hot technology areas, referring to Medidata Solutions and CEO Tarek Sherif.
Read
Applied Clinical Trials online in August features a Medidata Insights™ benchmark for protocol complexity. Part of a monthly series highlighting industry metrics, this edition focuses on the increasing complexity seen in clinical trials protocols in the past decade, and how despite continued warnings from experts on the topic, complexity continues on an upward, though admittedly less steep, trend.
Read
In the summer issue of International Clinical Trials, director of EMEA regional sales Richard Young discusses how technology is modernizing data management best practices, helping clinical researchers to better ensure trial integrity, lower trial costs, and make a risk-based monitoring approach a reality.
Read
FierceBiotech reports on the rapid growth of the eClinical market in China and other low-cost regions due to increased outsourcing and adoption of eClinical platforms like Medidata’s cloud-based solutions.
Read
In a Fortune article on the impact of health care legislation on technology, executive vice president of strategy and corporate development Bryan Spielman shares how results from a recent Medidata-sponsored study—which unveiled that 25% of all clinical trial procedures are potentially unnecessary—open opportunities to increase data efficiency.
Read
Outsourcing-Pharma.com spotlights Medidata’s CEO on effective M&A strategies for the clinical technology market, including targeting organizations with similar corporate cultures and complementary, rather than overlapping, capabilities.
Read
In a July Outsourcing-Pharma.com article, CEO Tarek Sherif comments on the future success of the eClinical space, and how its rapid growth and change is positioning Medidata to become "the leading provider of the clinical cloud."
Read
Pharmalot reports on the recent Medidata-sponsored study conducted at the Tufts Center for the Study of Drug Development, outlining key findings on unnecessary clinical trial procedures and ways to improve protocol feasibility.
Read
In a July article posted on PharmaPhorum.com, senior product marketing manager Joshua Pines and senior product director Stephen Young explain how adopting site quality management can streamline monitoring and improve data quality.
Read
In the summer issue of European Biopharmaceutical Review, manager of product management Sonia Araujo discusses how Europe is rewriting the rules and processes of pharmacovigilance in a move to make regulation more risk-based and proportionate, ultimately empowering patients and saving lives.
Read
The Medidata-sponsored Tufts study made eCliniqua's list of top news and product releases from DIA 2012, which took place June 24–28. President Glen de Vries says the study "emphasizes the increasing role technology, and the expertise around it, will continue to play in helping drug developers design, conduct and manage efficient and effective clinical trials."
Read
FierceCRO features the Medidata-sponsored study conducted by researchers from the Center for the Study of Drug Development at the Tufts University School of Medicine. The study examines data from 115 clinical trials and more than 22,000 procedures, and reveals that eliminating non-core procedures could save the industry up to $5 billion a year.
Read
PharmaTimes Online highlights the Medidata-sponsored Tufts study, which showcases how clinical trial sponsors spend $3–5 billion a year in unnecessary medical procedures on patients enrolled in their clinical trials.
Read
In the July issue of The New York Enterprise Report, president Glen de Vries sets the record straight about the misconceptions of owning a business in New York City, the greatest city in the world.
Read
On Outsourcing-Pharma.com, director of product management Michelle Marlborough discusses new Medidata sponsored study results, which reveal up to $5 billion in potential clinical trial cost savings and how better study design can help.
Read
Applied Clinical Trials online in July features Medidata Insights™ benchmarks on the increasing intensity of on-site monitoring. The annual trends of two critical monitoring efficiency metrics, Monitoring On-Site Rate and SDV Velocity, shows that site monitors are spending increasingly more days on-site per year and performing increasing amounts of SDV during each on-site day. The post is part of a monthly series highlighting industry metrics.
Read
In the June issue of European Pharmaceutical Contractor, vice president of partnerships and alliances Graham Bunn discusses the evolution of engagement in CRO and sponsor relationships, and how communication and technology can shape strategic partnerships in the future.
Read
In the June issue of PharmaVOICE, president Glen de Vries shares insight on the clinical cloud and how new technologies will shape the future of clinical trials.
Read
President Glen de Vries discusses the political landscape of healthcare, as well as the need for more effective and more valuable therapies, in the June issue of PharmaVOICE.
Read
Applied Clinical Trials online in June features a Medidata Insights™ benchmark for eCRF design complexity. Part of a monthly series highlighting industry metrics, this edition focuses on the alarming increase in complexity seen in recent years.
Read
As part of a series of videos commemorating the 20th anniversary of Applied Clinical Trials, Medidata's vice president of channel sales Steve Heath discusses the past and the future of the clinical trials industry.
Read
In the May issue of Pharma Focus Asia, director of China development Daniel Liu discusses the major regulatory practices related to conducting clinical trials in China, and how the quality of clinical research has improved due to the State Food and Drug Administration’s amendment of the Chinese Good Clinical Practice (GCP) guidance.
Read
Westat, an employee-owned research corporation, recently introduced Medidata Rave clinical data management services to support cancer Cooperative Groups as part of the Cancer Trials Support Unit (CTSU), a program of the National Cancer Institute (NCI). Westat presented at the Americas Medidata User Group (A-MUG) in May to share its Rave-related skills and approaches.
Read
The New York Times “The Boss” column features Medidata president Glen de Vries, highlighting how ballroom dancing has impacted his approach to business and helped him lead Medidata to its market-leading position today.
Read
Applied Clinical Trials online in May features a Medidata Insights™ benchmark for site performance. Part of a monthly series highlighting industry metrics, this edition focuses on the high percentage of clinical trial sites that fail to enroll a single patient.
Read
The Clinical Data Interchange Standards Consortium (CDISC) announces the release of the Protocol Representation "Toolkit," a standard format for study protocol data designed to save time and resources. Medidata Solutions will be providing the underlying technology for the Protocol Representation Model (PRM) Wizard, available in the next version.
Read
In this April eCliniqua feature, Medidata senior business consultant Jessica Dolfi examines how technological developments can streamline site negotiation processes to accelerate site budgeting and contracting.
Read
Applied Clinical Trials online in April features a Medidata Insights™ benchmark for data correction. Part of a monthly series highlighting industry metrics, this edition focuses on the remarkably low rate of post-capture data correction during clinical trials.
Read
Forbes spotlights Medidata Solutions for its market leadership in software for clinical trials.
Read
In its inaugural “Top 10 Biotech Techies” list, FierceBiotech honors Medidata president Glen de Vries and profiles him as builder of the clinical trial cloud.
Read
FierceBiotechIT reviews Arlene Weintraub’s profile on Medidata in Xconomy and a report from TheStreet, illustrating how the company is being “lauded on Wall Street.”
Read
Glenn Watt, Medidata’s vice president of information security and privacy, shares six key steps to reducing information security costs while ensuring sufficient risk controls in Information Management.
Read
Applied Clinical Trials online in March features Medidata Insights™ benchmarks for form design. Part of a monthly series highlighting industry metrics, this edition highlights a surprising lack of correlation between eCRF design timelines and the rate of eCRF reuse.
Read
Xconomy New York editor and veteran healthcare and life sciences writer Arlene Weintraub highlights how “Medidata Gains Raves on Wall Street,” driven by increasing demand for its cloud-based clinical development solutions and the vision and innovation of president Glen de Vries and CEO Tarek Sherif.
Read
In a March ComputerWorld feature examining agile development methods and outsourcing, Medidata’s senior vice president of research and development Andrew Newbigging discusses the company’s transition to agile and why developing in-house was the better strategy for meeting customer needs.
Read
Applied Clinical Trials online features a Medidata Insights™ benchmark on geographic shifts in enrollment. This unexpected trend in global subject enrollment was posted in February as part of a monthly series highlighting industry metrics.
Read
FierceBiotech IT highlights Medidata as “the cloud for clinical data” in this January article featuring president Glen de Vries’ Q&A in Bio-IT World.
Read
Applied Clinical Trials online features a Medidata Insights™ benchmark on source data verification, posted in January as the first of a monthly series highlighting industry metrics.
Read
Medidata president Glen de Vries chats with Bio-IT World’s chief editor about the history of the company and the focus on optimizing clinical trials from concept to conclusion, in this January Q&A on the state of e-clinical technologies.
Read
2011
In the fall issue of The Security Journal, Medidata's vice president of information security and privacy, Glenn Watt, discusses how organizations can view information security strategically in software development without falling victim to high costs.
Read
In the December issue of Journal for Clinical Studies, Medidata authors Jessica Dolfi and Sondra Pepe discuss the impact of the impending Sunshine Act on clinical trial sponsors.
Read
In eCliniqua’s December issue, Medidata’s Michelle Marlborough, director of product management, and Joshua Pines, senior product marketing manager, encourage protocol authors to think of themselves as data archaeologists, analyzing previous research to uncover and replicate best practices.
Read
Medidata’s vice president of partnerships and alliances, Graham Bunn, notes the qualities of effective CRO-sponsor relationships in Life Science Leader’s December issue.
Read
Medidata director of product marketing Stan Haavik, traces the development of interactive response technology (IRT) systems used in clinical trials for randomization, supply planning and implementation, in the December issue of Applied Clinical Trials.
Read
In the December issue of European Pharmaceutical Review, Medidata’s senior director of development Jeffrey Cohen and senior product marketing manager Joshua Pines discuss the standards created to help simplify integration between clinical technology solutions, and the external systems managing EHRs and medical images.
Read
ComputerWorld includes Medidata in a December article highlighting 10 selected firms that are looking to hire tech workers.
Read
Patrick Chassaigne, director, late phase solutions, explores the patients role in Phase IV studies and registries, in the November/December Year in Preview issue of PharmaVOICE. Vice president of clinical solutions Jeffrey Handen also weighs in on engaging the patient as a drug development partner and president Glen de Vries highlights three top trends impacting R&D.
Read (Patrick Chassaigne) | Read (Jeffrey Handen) | Read (Glen de Vries)
In a PharmExec guest blog post, Medidata director of late phase solutions Patrick Chassaigne discusses ways to drive patient participation in post-approval studies.
Read
In the autumn 2011 issue of International Clinical Trials, Medidata’s vice president of data operations Lori Shields discusses the importance of new technological tools that help sponsors and sites meet their budget needs and increase study efficiency.
Read
Medidata’s director of product management Michelle Marlborough comments on the importance of structured protocol designs to minimize costly mid-study amendments in the October 2011 issue of CenterWatch Monthly.
Read
Medidata's acquisition of Clinical Force, featured in the September issue of PharmaVOICE, leads to new clinical trial management solutions (CTMS) offerings. The issue also highlights product announcements for Medidata Standards Accelerator, Insights and Coder.
Read
Medidata senior vice president of development Andrew Newbigging named to PharmaVOICE 100 for his innovative efforts in clinical technology integration and commitment to advancing industry standards.
Read
Medidata’s vice president of data operations Lori Shields addresses the variance in clinical trial overhead rates across sites in the July issue of The CenterWatch Monthly.
Read
In a PharmaVOICE interview at the DIA Annual Meeting in Chicago, Medidata president Glen de Vries discusses ways to tackle challenges across the end-to-end clinical development process.
View
Medidata vice president of partnerships and alliances Graham Bunn discusses the recent acquisition of Clinical Force with Outsourcing-Pharma senior editor Nick Taylor live from the DIA Annual Meeting in Chicago.
View
Medidata director of product marketing Stan Haavik discusses the importance of process efficiency in clinical trial randomization in the June issue of PharmaVOICE.
Read
Medidata executive vice president of product and marketing Lineene Krasnow comments on new approaches to address the challenges of growing protocol complexity in the June issue of PharmaVOICE.
Read
Medidata vice president of product management Rick Piazza discusses the value of integration to maximize the benefits of clinical development technologies in the June issue of PharmaVOICE.
Read
In the summer issue of European Pharmaceutical Contractor, Medidata senior product marketing manager Joshua Pines discusses how life science organizations can maximize the impact of EDC adoption by revisiting their internal processes and analytics tools.
Read
Boston University’s Dr. Iain Cockburn discusses the use of Medidata’s trial planning data in a National Bureau of Economic Research study analyzing the increasing costs of clinical trials in this May article from ClinPage.
Read
Medidata vice president of partnerships and alliances Graham Bunn discusses CRO industry trends, including the importance of strategic relationships with sponsors, in the May issue of Contract Pharma.
Read
The Cancer Letter interviews Medidata president Glen de Vries about the implementation of Medidata Rave by the National Cancer Institute Cooperative Groups. Published with permission from The Cancer Letter.
Read
CWWeekly's “Insider Insights” spotlights Medidata in an in-depth interview with Medidata president Glen de Vries.
Read
Medidata associate product manager Keyur (Kevin) Shroff discusses six steps to streamlining the contracting of sites for clinical studies in the March issue of Journal for Clinical Studies.
Read
Medidata director of late phase solutions Patrick Chassaigne weighs in on the growing importance of observational research in the March issue of R&D Directions.
Read
Medidata vice president of regulatory policy Pat Beers Block and senior product director Steve Young provide commentary on the high cost and questionable impact of 100% SDV in the February issue of The CenterWatch Monthly.
Read
Medidata senior director of product marketing Ron Rubinstein discusses why EDC offers an elegant solution to reducing the burden of SAE reporting for both sites and sponsors in the January/February issue of Bio-IT World.
Read
2010
Medidata business consultant Jessica Dolfi explains how to optimize a site budget in a diverse and rocky world in the December issue of Scrip Clinical Research.
Read
Medidata senior product director Steve Young and director of strategic initiatives Ashwin Mundra equip clinical organizations on the right tools to execute risk-based site monitoring in the November/December issue of VIEW on E-Solutions.
Read
ClinPage reports on October 22 on Medidata's EDC enhancements and how the company continues to innovate briskly.
Read
Medidata vice president of channel sales and head of EMEA Steve Heath focuses on Australia as an emerging global clinical research destination in the September issue of the Journal for Clinical Studies.
Read
Medidata senior product director Steve Young and director of strategic initiatives Ashwin Mundra discuss risk-based site monitoring and partial source document verification as the new paradigm in the September issue of European Pharmaceutical Contractor.
Read
Peking University Clinical Research Institute partners with Medidata to support China's Drug Innovation and Development initiative.
Read
Medidata president Glen de Vries explains to PharmaVOICE on the show floor of the DIA Annual Meeting how Software as a Service (SaaS) can improve the clinical development process as well as optimize sponsors' R&D investments.
View
Medidata vice president of operational excellence Douglas Bain provides insight on the future of e-sourcing in a September 21 article by eCliniqua.
Read
Medidata director of strategic initiatives Ashwin Mundra discusses the new paradigm in site monitoring in the September issue of Life Science Leader.
Read
Medidata vice president of partnerships Graham Bunn named to PharmaVOICE 100 as a CRO and technology partnership visionary and for inspirational industry leadership.
Read
Medidata vice president of operations Lori Shields and manager of data quality and analytics Rafael Campo discuss reimbursement and protocol complexity trends in the June issue of VIEW on Clinical Operations.
Read
Medidata business consultant Jessica Dolfi, manager of data quality and analytics Rafael Campo and other industry experts share how study managers can master currency fluctuations in global clinical trials in the June issue of Applied Clinical Trials.
Read
FierceBiotech IT reports on June 18 the unveiling of Medidata Balance, a randomization and trial supply management solution, at the Drug Information Association (DIA) meeting.
Read
Medidata president Glen de Vries discusses two new products announced at the DIA Meeting in Washington, D.C., with Bio-IT World on June 16.
Read
Drug Discovery & Development reports on June 16 that Medidata and Aris Global announced the data sharing for EDC and Safety Report Systems.
Read
ClinPage reports on June 15 that the Medidata and SAS alliance provides strong clinical data custody.
Read
Medidata president Glen de Vries talks about running a business by predicting industry needs for ten years in the future and the excitement of taking the company through an IPO during the most challenging economic climate in history in the June issue of Scrip Clinical Research.
Read
Medidata vice president of partnerships and alliances Graham Bunn provides commentary on how CROs are riding the R&D recession wave in a CRO industry update in the June issue of Contract Pharma.
Read
Applied Clinical Trials reports on June 3 that Medidata welcomed the first Australian CRO to the ASPire to Win channel partner program.
Read
Medidata senior client relations specialist Sondra Pepe provides insight on managing a global clinical trial in a June 1 article by Applied Clinical Trials.
Read
FierceBiotech IT reports on May 14 that Medidata and Aris Global have integrated the ARISg solution for pharmacovigilance and clinical safety with Medidata Rave for electronic data capture, management and reporting.
Read
Medidata client services principal Thomas Ermlich explains how companies can maximize their eClinical strategies through process optimization, technology implementation and industry knowledge in the spring issue of European BioPharmaceutical Review.
Read
FierceBiotech IT reports on April 10 that City of Hope selected Medidata Rave for its internal clinical trials after evaluating ten electronic data capture solutions.
Read
Medidata vice president of alliances Anne Zielinski discusses what makes the right menu for clinical trials technology in the April issue of Life Science Leader magazine.
Read
Medidata vice president of information security and privacy Glenn Watt shares lessons from the trenches of clinical development technology for cloud computing security in the January issue of Bio-IT World.
Read
2009
Medidata vice president of implementation services David Gemzik and other industry experts discuss the CDISC protocol representation model for optimizing clinical research via standardization in Volume 4 of Drug Development.
Read
Roche explains how it managed the successful introduction of its new EDC system, Medidata Rave, in the autumn issue of Data Matters, an ACDM newsletter.
Read
Medidata vice president of implementation services David Gemzik offers tips for a healthy clinical trial
with the help of high-quality protocol development programs in the December issue of European Pharmaceutical Contractor.
Read
Medidata vice president of alliances Anne Zielinski examines if Contract Research Organizations (CROs) and Electronic Data Capture (EDC) are a match made in heaven or an uneasy alliance in the November/December issue of Contract Pharma.
Read
Medidata vice president of implementation services David Gemzik and senior product marketing manager Sean Cheng explain why sponsors need an integrated, closed-loop clinical process in the November issue of VIEW on E-Solutions.
Read
Medidata vice president and head of EMEA Steve Heath and senior director of quality assurance Tony Hewer discuss how technology can aid in the relationship between society, regulators and the life sciences industry in the November issue of Life Science Leader.
Read
Medidata vice president and head of EMEA Steve Heath explains how small and mid-sized biotech and pharmaceutical companies can continue to build an eClinical strategy in today's economy in the autumn issue of the Journal for Clinical Studies.
Read
Medidata vice president and head of EMEA Steve Heath provides the editorial advisory keynote for the July issue of the Journal for Clinical Studies.
Read
Medidata vice president Lori Shields honored in PharmaVOICE 100 for innovation, creativity and inspirational leadership.
Read
Medidata vice president of implementation services Mukhtar Ahmed looks at the growth and challenges of the Asia Pacific region in European Pharmaceutical Contractor.
Read
Medidata senior client relations specialist Sondra Pepe provides an overview of the proposed Sunshine Act legislation and how pharmaceutical, biotechnology and medical device companies can prepare for the potential impact of these new federal requirements in Pharmaceutical Executive.
Read
Medidata explains how electronic protocol solutions can save time and costs for sponsors in eCliniqua.
Read
Medidata senior director of product marketing Ron Rubinstein and president of MonitorForHire.com, Scott Freedman, explain how EDC has changed clinical monitoring in VIEW on Clinical Operations.
Read
Medidata president Glen de Vries and SAS global director of health and life sciences market segments Jason Burke discuss the current state of health business innovation, particularly around providing solutions for clinical trials and drug development in a Bio-IT World podcast.
Read
Medidata director of late phase solutions Patrick Chassaigne and vice president of quality assurance Fran Nolan explore how EDC can meet the regulatory challenges of post-approval research in the Good Practice Clinical Journal.
Read
AstraZeneca's use of Medidata Rave receives honorable mention from Bio-IT World magazine's fifth Best Practices Awards program.
Read
Medidata head of EMEA Steve Heath provides commentary on India as an emerging market for clinical trials in R&D Directions.
Read
Medidata director of late phase solutions Patrick Chassaigne explains how EDC can help power post-marketing studies in the Journal for Clinical Studies.
Read
Medidata vice president of global CRO partnerships Graham Bunn defines what global means and provides commentary on global development for drug developers in PharmaVOICE.
Read
Medidata general manager of Trial Planning Solutions Ed Seguine explains why it's time to change protocol design and how eProtocol will provide a radical shake-up of old processes and lead to improved productivity in International Clinical Trials.
Read
Medidata supports the efforts of the American National Standards Institute (ANSI) in facilitating the use of electronic health information to support global clinical research activities.
Read
Medidata selected as finalist for the Software & Information Industry Association's (SIIA) 24th Annual CODiE Awards, which celebrate outstanding achievement and vision in the software, digital information and education technology industries. Medidata Rave's Web Services API was among 5 finalists nominated in the Best Medical and Health Information Product category.
Read
Medidata vice president of global CRO partnerships Graham Bunn discusses the world of opportunity for contract research companies in choosing sites for clinical trials in R&D Directions.
Read
Medidata vice president of operations for Trial Planning Solutions Lori Shields provides expert commentary on process improvements for investigator payments in PharmaVOICE.
Read
Medidata senior director of product marketing Ron Rubinstein offers three key ingredients to cost effective clinical system interoperability in Bio-IT World.
Read
Bio-IT World explains how Medidata avoids the pitfalls of EDC training.
Read
Medidata head of EMEA Steve Heath takes a look at electronic data capture solutions in Next Generation Pharmaceuticals.
Read
2008
Alan Louie, research director at Health Industry Insights, an IDC company, offers his perspective on how Medidata brings intelligent design to clinical trials.
Read
Senior research fellow at the Tufts Center for the Study of Drug Development Ken Getz and Medidata general manager of trial planning solutions Ed Seguine address the cause, not symptoms, of rising clinical trial delays and costs in a Bio-IT World podcast.
Listen
Medidata senior vice president of development Keith Howells explores the opportunities, risks and technical requirements needed for an integrated EDC environment in IDrugs.
Read
Medidata vice president of knowledge management Daniel Mudgett and manager of knowledge management Ashwin Mundra discuss how integrated eLearning enables efficient and streamlined global trials in VIEW on E-Solutions.
Read
Bio-IT World discusses how Medidata spurs innovation with Developer Central.
Read
Medidata vice president of global operational excellence Doug Bain provides commentary on CDASH as the final piece in the end-to-end eClinical interoperability puzzle in Clinical Trials Today.
Read
Medidata vice president of integrations development Andrew Newbigging discusses how ePRO and EDC are perfect together in Applied Clinical Trials.
Read
Medidata general manager of trial planning solutions Ed Seguine senior data analytics specialist, Rafael Campo, and other industry experts assess protocol complexity and the impact of protocol design changes on clinical trial performance in the American Journal of Therapeutics.
Read
Medidata's corporate compliance officer and vice president of global regulatory affairs & quality assurance Earl Hulihan provides a perspective on the FDA's updated guidance on the use of computer systems in clinical research in Applied Clinical Trials.
Read
ClinPage discusses the use of reality-based budgeting to optimize protocols with Ed Seguine, Medidata general manager of trial planning solutions.
Read
Medidata Solutions' R&D head Keith Howells recognized by PharmaVOICE for industry vision.
Read
Medidata general manager of trial planning solutions Ed Seguine discusses the efficiencies of EDC and eProtocols in View on Clinical Operations.
Read
ClinPage discusses protocol optimization and EDC with Medidata's acquisition of Fast Track.
Read
Medidata and other industry thought leaders share the steps to shaping success in adaptive clinical trials in a Future Pharmaceuticals podcast.
Listen | Read
PharmaTimes reports on Medidata's new protocol development and planning tools.
Read
Bio-IT World reports on Medidata's move 'upstream' with the Fast Track acquisition.
Read
ClinPage explains how Medidata is raising the bar with its updated EDC offering.
Read
Medidata executives explain how late phase studies benefit from EDC in Applied Clinical Trials.
Read
Medidata executives provide insight on China's SFDA commitment to regulatory transparency in Bio-IT World.
Read
ClinPage reports on the INC Research and Medidata alliance.
Read
2007
Bio-IT World explains why Wyeth selected Medidata Rave as its EDC standard.
Read
Medidata vice president of Product Strategy Hugh Levaux discusses the interplay between adaptive clinical trials and e-clinical architecture on the VIEW on E-Solutions.
Read
Medidata receives rave reviews from R&D Directions. Reprinted with permission from R&D Directions, October 2007.
Read
Fast Track vice president of clinical strategy Fredric Cohen discusses the considerations for building or buying critical eClinical applications in Next Generation Pharmaceutical.
Read
Fast Track vice president of clinical strategy Fredric Cohen describes the role and importance of the clinical protocol in drug development in Next Generation Pharmaceutical.
Read
ClinPage reports on Enterprise Deal With Wyeth.
Read
Fast Track vice president of clinical strategy Fredric Cohen discusses smart clinical research protocols in the Journal of Clinical Research Best Practices.
Read
Medidata vice president of Product Strategy Hugh Levaux describes how EDC meets the needs of postmarketing research in Applied Clinical Trials.
Read
Medidata vice president of Global Regulatory Initiatives and Pharmacovigilance Bart Cobert, Ph.D., provides a contrarian's point of view on drug safety in the Food and Drug Law Journal, Volume 62, Issue 3. With permission from FDLI.
Read
Data from Fast Track confirms that more sites are asking for separate startup fees and that oncology trials are leading the way, as reported in Applied Clinical Trials.
Read
Medidata Solutions CEO and co-founder Tarek Sherif selected as PharmaVOICE 100 Most Inspiring People in the Life-Sciences Industry.
Read
Mark Uehling of ClinPage.com reveals how Medidata and statistical powerhouse SAS are raising the bar on integrations and how Medidata Rave is bringing customers closer to a complete end-to-end solution.
Read
Medidata vice president of Global Regulatory Affairs and Quality Assurance Earl Hulihan offers Five Lessons in Outsourcing in Good Clinical Practice Journal.
Read
Medidata CTO Glen de Vries discusses the role of EDC in adaptive clinical trials in the supplement to Applied Clinical Trials.
Read
Crain's New York Business tracks Medidata as one of the fastest-growing homegrown technology firms.
Read
Fast Track vice president of operations Lori Shields spotlights research fees and trends in cost-per-subject pricing in the Journal of Clinical Research Best Practices.
Read
Medidata CTO Glen de Vries discusses why EDC is not a replacement for CDMS but is the next logical evolution in PharmaVOICE.
Read
Fast Track CEO Ed Seguine explains what's different now in EHR and subject recruitment in Bioexecutive International.
Read
2006
Medidata CTO Glen de Vries examines the challenges and opportunities of managing clinical data and medical records across borders in Pharmaceutical Executive Europe.
Read
Read
Fast Track CEO Ed Seguine explains how to juggle clinical development in Next Generation Pharmaceutical.
Read
Medidata co-founder and Chief Medical Officer Ed Ikeguchi, MD, discusses "Global clinical trials: challenge or opportunity?" in Next Generation Pharmaceutical magazine.
Read
Medidata CMO Ed Ikeguchi's insight on why 'China welcomes EDC' is profiled in R&D Directions.
Read