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Educational Underwriters

To learn about becoming an Educational Underwriter, please contact Eric Morrin, Senior Business Development Manager, at 212-400-6228 or emorrin@exlevents.com.

Corementum

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Corementum

Corementum helps clients with the Trial Master File Management and Regulatory Submissions Operations necessary to acquire agency approval for regulatory applications in the biotech and pharmaceutical organizations. We help companies who conduct clinical trials to standardize and organize their information that is compliant with the regulations set by the agencies. Corementum assists clients with information management but with compliance, regulation and timely approval of clinical trials by the agency. We are passionate about helping our clients receive the agency approval they need in a timely manner. We make it work the first time!

HSRAA

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HSRAA

Established in 1981, the not-for-profit Health Sciences Records and Archives Association (HSRAA) provides support, guidance, and networking for those working in healthcare organizations. Members work with GxP records from their creation to archiving and destruction.

The Health Sciences Records and Archives Association’s aims are to:

  • Raise the profile of records management and archiving as business critical activities;
  • Improve the professional competencies of records managers and archivists;
  • Encourage the consistent interpretation of pertinent laws, regulations, and guidance; and
  • Influence the regulatory environment.

The association welcomes Records Managers, Archivists, Regulators, Suppliers, and Consultants that work in the Health Sciences industry. https://the-hsraa.org/

Just in Time GCP

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Just in Time GCP

Just in Time GCP supports small and mid-size pharma companies and CROs in managing their Trial Master Files. Whether you are anticipating a regulatory inspection, need resourcing for routine quality oversight of your TMFs or are planning the implementation of a TMF system, Just in Time GCP can support you. We have extensive industry experience in clinical operations and truly understand the complexities of trial management and drug development. We partner with your organization in ensuring that your TMFs are inspection-ready. We take the stress out of TMF management.

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.

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