Nous contacter

eTMF Software Systems

A trial master file (TMF) contains essential documents and artifacts associated with a clinical trial which are subject to compliance with ICH GCP, FDA 21 CFR Part 11 and other regulatory requirements. The TMF must not only contain adequate and accurate data, but it must also be organized in a manner suitable for evaluation by inspectors, and sharing with clinical study team members both internally and externally. MasterControl goes beyond mere document management by providing an eTMF software system based on the TMF Reference Model that is designed to enable real-time visibility into the status of all activities pertaining to a clinical study.


Watch Videos: Learn More About Clinical Quality Management Systems (CQMS)

Download Free Clinical Quality Management Resources

Informations sur le produit

Discover how MasterControl Clinical Management Software can manage your Clinical Quality Management Software Systems (CQMS) process, all while mitigating risk, improving speed-to-market, and generating ROI.

Données techniques produits
Données techniques produits
Données techniques produits
Questions-réponses

Demos & Toolkits

Get in-depth, comprehensive resources to guide development of your CQMS program.

Données techniques produits
Démonstrations interactives et en direct
  • MasterControl offers the most complete choice of integrated solutions covering all core areas necessary to successfully maintain quality and compliance processes, as well as a variety of services based on industry best practices.
Données techniques produits
Kits d'outils

Educational Materials

Get insider information about the most relevant issues in Clinical Quality Management Software Systems (CQMS) today, and how to navigate and overcome the complexities of FDA and ISO compliance.

Données techniques produits
Livres blancs
Educational Materials
Modèles gratuits

Educational Materials

Livre électronique
  • Depuis 2000, la conformité règlementaire s'est modernisée grâce à l'essor des nouvelles technologies. Ce livre électronique identifie 16 lois et initiatives qui ont contribué à cette évolution. Il décrit l'impact de la technologie sur l'amélioration sur les deux plans, tant les entreprises que les agences réglementées, afin de réduire les difficultés et les coûts liés à la mise en conformité, au cours de la dernière décennie.


The Value of a Compliant, Connected eTMF Software System


Managing thousands of clinical documents, tasks and processes using a paper-based or hybrid TMF system can be overwhelming and can introduce errors and oversights that put your clinical trial at risk for noncompliance. An eTMF software system can provide an industry best practice approach to document management which allows you to gain the insight you need to efficiently manage your clinical trials and accelerate your time to market. MasterControl's eTMF software systems are designed to effectively manage eTMF processes and integrate them with other quality processes critical to regulatory compliance.


Benefits of MasterControl eTMF Software

  • Designed by Experts: MasterControl TMF JumpStart is a configuration that has been developed by MasterControl with the guidance of a member of the DIA SIAC. This configuration of document types and metadata based on the DIA TMF Reference Model was designed to promote a common configuration across the industry for clinical trial document management.
  • Simple Implementation: Using the MasterControl TMF JumpStart decreases implementation time and ensures that companies get a more standard configuration.
  • Mobile Access: External light users and mobile users can quickly access information in the clinical management software system that is critical to their roles (monitor, auditor, investigators) as well as enhance the flow of information and execution of tasks, thereby reducing cycle time (i.e., review, approval and training).


Features of MasterControl eTMF Software

  • MasterControl eTMF software systems include a configuration that has been developed by MasterControl with the guidance of a member of the DIA SIAC. This configuration of document types and metadata based on the DIA TMF Reference Model was designed to promote a common configuration across the industry for clinical trial document management.
  • Using the MasterControl eTMF software system decreases implementation time and ensures that companies get a more standard configuration.
  • External light users and mobile users can quickly access information in the clinical management software system that is critical to their roles (monitor, auditor, investigators) as well as enhance the flow of information and execution of tasks, thereby reducing cycle time (i.e., review, approval and training).
  • The MasterControl eTMF Reference Model configuration is based on the DIA Reference Model. Using this model will increase efficiency and provides a central location for all required TMF documents.
  • MasterControl Taxonomy Organizers are designed to create folder structures based on metadata populated within each document to automate the placement and creation of electronic TMF organizers.
  • MasterControl provides various methods for batch importing and exporting of content to and from the clinical management system to facilitate the relationship between sponsors and CROs.
  • MasterControl TMF includes predefined rights access configuration for sponsors, CROs and sites. Documents, as well as collections of documents, can be easily shared with internal and external partners.
  • MasterControl GuestConnect feature of Documents allows a user to invite external parties to upload content into the system in a controlled method using a placeholder which must then be released by documentation manager upon verification.
  • The MasterControl GuestConnect feature of Documents allows a user to invite system users as well as external parties to controlled "collaboration spaces," enabling them to work collaboratively on documents.


TMF Management Challenges

MasterControl TMF Solution


Difficulty managing the high volume and granularity of all documents that make up a clinical trial master file.


The MasterControl TMF Reference Model JumpStart® configuration is based on the DIA Reference Model. Using this model will increase efficiency and provides a central location for all required TMF documents.


Organizing TMF documentation in a consistent structure to facilitate placement and location of information.

MasterControl Taxonomy Organizers are designed to create folder structures based on metadata populated within each document to automate the placement and creation of electronic TMF organizers.


Transferring high volume batches of information and content to and from various sources (i.e., internal, CROs, sponsors, clinical sites).

MasterControl provides various methods for batch importing and exporting of content to and from the clinical management system to facilitate the relationship between sponsors and CROs.


Sharing of critical study and site-related documentation with partners (i.e., sponsors and CROs) and sites as needed.

MasterControl TMF includes predefined rights access configuration for sponsors, CROs and sites. Documents, as well as collections of documents, can be easily shared with internal and external partners.


Exchanging documents between partners (i.e., sponsors and CROs) and sites in a controlled environment.

MasterControl GuestConnect® feature of Documents allows a user to invite external parties to upload content into the system in a controlled method using a placeholder which must then be released by documentation manager upon verification.

Collaborating on, editing, reviewing and approving documents with both internal and external partners.

The MasterControl GuestConnect® feature of Documents allows a user to invite system users as well as external parties to controlled "collaboration spaces," enabling them to work collaboratively on documents.


En savoir plus sur les logiciels de contrôle des documents

Pour en savoir plus sur les logiciels de contrôle des documents de MasterControl, n'hésitez pas à contacter un représentant MasterControl.