Cencora solution

PhlexTMF for Contract Research Organizations (CROs)

Give your customers the confidence of TMF health from plan to archive
  • Pharma
  • Global
  • Drug research and clinical development support

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PhlexTMF is the ideal eTMF for Contract Research Organizations


In today’s marketplace, the electronic Trial Master File (eTMF) is viewed as a competitive differentiator for contract research organizations (CROs).

eTMFs offer CROs the opportunity to:

  • Enable your sponsor oversight in an easy and cost-effective way
  • Increase inspection readiness through management of timeliness, quality, and completeness
  • Provide a compliant eTMF offering to your current and potential sponsor partners
With decades of Trial Master File experience, Cencora has a unique understanding of the industry’s TMF challenges and opportunities, and we partner with our clients to complement your capabilities with our expertise to deliver measurable results. 

Our best-in-class eTMF, PhlexTMF, is optimally designed to very efficiently enable teams to work within the system, and flexible enough to support multiple client standards, conventions, and TMF structures – key criteria for any CRO looking to select the right eTMF system and TMF partner.

At Cencora, we are committed to delivering Trial Master File (TMF) services that meet the highest standards of data protection, confidentiality, and compliance with applicable global privacy regulations. As your trusted Contract Research Organization (CRO) partner, we assure you that our TMF services are designed, implemented, and continuously reviewed to align with international and national data protection laws, regulations, and industry best practices. CRO Privacy Assurance Statement

eTMF is a commercial imperative for CROs

Many CROs offer an eTMF capability, and they report a broad range of benefits related to audit and inspection readiness.
Most sponsors are comfortable with, and many prefer that, their CRO manage eTMF(s) in their system on their behalf.
There is a substantial market opportunity for CROs to become more competitive by becoming eTMF-enabled.
CROs report that most requests for proposals ask for an eTMF capability to be provided by potential CRO partners.

Guide

Reasons why CROs are choosing our eTMF

Get more details around the reasons contract research organizations (CROs) and academic research organizations (AROs) are turning to Cencora, such as:
  • The industry’s only advanced eTMF SaaS solution built around the business practices of CROs and AROs
  • Pre-configured, CRO- and ARO-specific workflows to accelerate time-to-value and streamline TMF operations
  • Cencora’s commitment to a genuine partnership and support to help your customers achieve ongoing compliance and inspection-readiness

Inspection-readiness

We offer you and your customers optimum inspection-readiness through superior collaboration, communication, and workflows:

  • Manage multiple TMF structures to meet the filing needs of clients. Easily apply study-specific logic to the default TMF structure.
  • Provide highly-configurable workflows and auto-assign activities and tasks to your staff based on priority
  • Report on the completeness of an eTMF at any point in time and better facilitate TMF quality review
  • Offer site access for electronic Investigator Site File (ISF) and provide a cost-effective, long-term archiving solution for you or your sponsors
  • Leverage our market leadership and recognition, presentations, and proposal content to drive new business
  • Partner through every phase of an implementation to share our knowledge on how to support the broad range of industry expectations for paper and electronic TMF content management with accelerators, such as templates to capture client conventions
 

Connect with our TMF experts to learn more


Get in touch to learn about how our solutions can help accelerate better health outcomes. Whether you have questions or just need more information, our experts are here to assist you.

Hos Cencora forstår vi at effektiv håndtering av Trial Master File (TMF) er essensiell når man skal lykkes med klinisk utprøving, være klar for regulatorisk inspeksjon og gjennomføre langsiktig dokumentstyring. Som en global leverandør av TMF-tjenester er det vår forpliktelse å sørge for at alle personopplysninger som behandles på våre TMF-plattformer og -tjenester, overholder gjeldende personvernlovgivning i hele verden. TMF Solutions' globale personvernerklæring