Interested in becoming a Sponsor? Apply Here!

Sponsors

Would you like to learn more about sponsorship and exhibiting opportunities at the 6th European Trial Master File (TMF™) Summit? Please contact Eric Morrin, Senior Business Development Manager, at +1 212-400-6228 or emorrin@exlevents.com.

MasterControl

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MasterControl

MasterControl quality management software and services enable research and manufacturing companies in the life sciences to increase compliance while reducing time to market. MasterControl offers solutions for the entire enterprise, including clinical, regulatory and quality management with document control (e.g. GxP); document management (e.g. eTMF); study management; monitoring; audit management; regulatory submission management; training management; supplier management; deviation management; CAPA; and more.

Medidata

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Medidata

Medidata is reinventing global drug and medical device development by creating the industry’s leading cloud-based solutions for clinical research. Through our advanced applications and intelligent data analytics, Medidata helps advance the scientific goals of life sciences customers worldwide, including over 850 global pharmaceutical companies, biotech, diagnostic and device firms, leading academic medical centers, and contract research organizations.

The Medidata Clinical Cloud® brings a new level of quality and efficiency to clinical trials that empower our customers to make more informed decisions earlier and faster. Our unparalleled clinical trial data assets provide deep insights that pave the way for future growth. The Medidata Clinical Cloud is the primary technology solution powering clinical trials for 18 of the world’s top 25 global pharmaceutical companies and is used by 18 of the top 25 medical device developers—from study design and planning through execution, management, and reporting.

Montrium

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Montrium

Montrium is a global leader in regulated electronic content management solutions and GxP Consulting Services for the Life Sciences. With over 10 years of experience in the clinical research and drug development arena, our team has developed a range of intelligent and dynamic solutions for document and quality management. eTMF Connect, an Electronic Trial Master File (eTMF) solution, centralizes and standardizes your clinical records enabling both sponsors and CROs to contribute and access information in real time. eTMF Connect has been built to:

  • Facilitate the exchange of clinical trial information to all stakeholders
  • Accurately track the progress of eTMF Completeness
  • Quickly comply with Regulatory Requirements, Audits and Inspections
  • Accelerate Study & Site Startup
  • Enhance the Quality and Integrity of Clinical Documentation

NNIT

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NNIT

NNIT is an international consultancy in the development, implementation, validation and operation of IT for the life sciences industry.

We create value for our clients by treating their IT as if it were our own and, of course, we meet the industry’s strictest requirements for quality.

We apply the latest advances in technology to make our clients’ software, business processes and communication more effective.

Phlexglobal

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Phlexglobal

Phlexglobal are the Trial Master File (TMF) experts, and pioneers in the provision of innovative, flexible and technology-enabled TMF solutions and services.

A specialist provider of electronic Trial Master File (eTMF) solutions and other support services to the global clinical research market, we offer a unique combination of technology, quality and services that deliver a range of flexible, targeted solutions to the life science industry.

Syntel

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Syntel

Syntel (Nasdaq:SYNT) is a leading global provider of automation-driven IT and knowledge process services. Syntel helps global enterprise build agile, efficient technology infrastructures that blend legacy business models with disruptive digital innovations. Our 23,000+ employees believe in building collaborative partnerships and long-term business value for clients by investing in IP, solutions and industry-focused delivery teams with deep domain knowledge. Learn more at www.syntelinc.com.

TMC

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TMC

TMC are hands-on problem-solvers who relish the fact that each project brings its own challenges. After assessing a client’s needs, we assign a team with precisely the expertise needed to design the ideal solution and follow it through to a successful conclusion.

Our services start with product manufacturing and pre-clinical testing, through full product development to obtaining global Marketing Authorisations. Post-approval our support continues with regulatory maintenance, pharmacovigilance, scientific service and much more.

TransPerfect

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TransPerfect

TransPerfect provides a collaborative web-based platform for study start-up and eTMF that enables sponsors, CROs, IRBs, central laboratories and other vendors to maintain and update clinical trial documentation in a secure online environment. TransPerfect's Life Sciences division is dedicated to working with clients on a global, collaborative level, supporting a wide range of requirements including product licensing and alliance management, endpoint adjudication, eTMF review/reconciliation, and pharmacovigilance.

Veeva Systems

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Veeva Systems

Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 200 customers ranging from the world's largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices in Europe, Asia, and Latin America. For more information, visit www.veeva.com.

Wingspan Technology, Inc.

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Wingspan Technology, Inc.

Wingspan Technology, a QuintilesIMS company, provides an ECM platform for the life sciences industry in a high-performance, scalable, validated cloud environment. Our industry-leading eTMF process is used by sponsors and CROs of all sizes to manage trials from planning through archival. Wingspan provides the transparency needed to understand TMF health and inspection readiness, along with tools to support and measure the productivity of eTMF processes. As a result, eTMF contributed significantly to supporting our clients’ record of successful health authority inspections.

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