Støtte for legemiddelforskning og klinisk utvikling

Trial master file software and services

Vi utvider aktivt innholdet vårt for følgende løsninger.  Kom snart tilbake for å utforske de nye sidene:

  • Rådgivning om klinisk utvikling
  • Regulatorisk støtte
  • Programvare og tjenester for PV
  • Programvare og tjenester for kliniske data
  • Operasjonelt design for kliniske studier
  • Logistikk for klinisk utprøving
  • Produktstrategi for kliniske studier 
  • Klinisk forskningsnettverk

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Guide

Five reasons why your TMF isn’t inspection-ready

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We're here to answer questions and to support your drug research and clinical development needs.

Solutions to achieve TMF health and maintain inspection-readiness

Managing a Trial Master File (TMF) can be a complex undertaking, presenting challenges like maintaining clinical data integrity and security, efficiently managing vast amounts of clinical trial documentation, and ensuring that all documents are complete and up-to-date. These challenges often require vast amounts of resources and lead to increased operational costs and potential delays in clinical trials. 

At Cencora, we offer global coverage with help from hundreds of TMF experts, ready to help you simplify and streamline the entire TMF management process. Our comprehensive suite of TMF solutions work to maintain the inspection-readiness of your TMF, while freeing up your internal resources to focus on advancing clinical trials.

  • Streamline management of TMF processes throughout the study life cycle, from initial planning and study startup to closeout, inspection, and final archive. 
  • Free up your internal TMF resources with our expert TMF study project leads. Achieve seamless, precise TMF migrations and imports, regardless of scale.
  • Integrate with your own workflows and best practices with easily customizable clinical eTMF software. 
  • Incorporate business-enabling technology advances such as machine learning and natural language processing (NLP) via a steady cadence of software releases.
AI-assisted indexing makes TMF management faster, better, and easier. Download our AI case study to read about how our PhlexGlobal eTMF software generated the following results for a mid-sized pharmaceutical company. You can also view our AI Privacy and Data Protection Assurance Statement.
95%
Document classification
accuracy rate
16%
Reduction in 
processing time
6.25
Hours saved per
1000 documents
scanned

Løsninger

TMF-kvalitetsanmeldelser og varmekart
Unngå unødvendige forsinkelser, kostnader og innsats med gjennomgang av bransjens ledende TMF-eksperter og få synlighet og innsikt i TMF-helse
TMF-dokumentbehandling
Dokumentstøtte tilgjengelig når du trenger det, der du trenger det
  • Støtte for legemiddelforskning og klinisk utvikling
  • Farmasøytiske produsenter
  • Globalt
TMF-studieprosjektledere
Utvid raskt dine interne Trial Master File (TMF)-ressurser med TMF-ekspertise når som helst og hvor som helst
  • Støtte for legemiddelforskning og klinisk utvikling
  • Farmasøytiske produsenter
  • Globalt
TMF-risikovurdering
Våre bransjeeksperter gir en helhetlig gjennomgang og vurdering av teknologien, menneskene, prosessene og strategien din for å identifisere problemer som kan utgjøre en risiko under inspeksjoner.
  • Støtte for legemiddelforskning og klinisk utvikling
  • Farmasøytiske produsenter
  • Globalt
TMF-migrasjoner og -importer
Bidra til å sikre at du oppfyller standarder for god klinisk praksis (GCP) og regulatoriske krav for viktige dokumenter.
  • Støtte for legemiddelforskning og klinisk utvikling
  • Farmasøytiske produsenter
  • Globalt
Støtte for TMF-fusjoner og oppkjøp (M&A)
Få et sant bilde av det innkjøpte produktets beredskap for inspeksjon eller innlevering, og løs eventuelle problemer. Reduser risiko, effektiviser regulatoriske innsendinger og forbedre den generelle suksessen til oppkjøpet ditt.
  • Støtte for legemiddelforskning og klinisk utvikling
  • Farmasøytiske produsenter
  • Globalt

Products

Global

PhlexTMF Enterprise

Innovative TMF management for higher-quality output.

Global

PhlexTMF Express

Improve inspection-readiness with software built on TMF best practices.

Global

PhlexTMF for Viewing

Viewable, inspectable eTMF archive for closed studies from your CRO.

Global

PhlexTMF for CROs

Give your customers the confidence of TMF health from plan to archive.

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Discover more capabilities

Commercialization support

Build a foundation for a successful product launch and accelerate your speed-to-market across the globe with strategic, integrated, and proactive solutions.

Patient access and adherence support

Address potential barriers to access and increase the speed-to-therapy with our suite of pharma patient support services.

Logistics and warehousing

Leverage our global network, specialized packaging, and customs expertise to ensure safe, secure storage and timely delivery worldwide.

Want more information? 

We're here to answer questions and to support your drug research and clinical solution needs.
At Cencora, we understand that effective Trial Master File (TMF) management is a cornerstone of successful clinical trial execution, regulatory inspection readiness, and long-term document governance. As a global provider of TMF services, we are fully committed to ensuring that all personal data processed within our TMF platforms and services complies with applicable privacy and data protection laws worldwide. TMF Solutions Global Privacy Statement