Solutions by Industry


MasterControl builds solutions to address particular needs in specific industries such as pharmaceuticals, medical devices, clinical laboratories and more. These solutions allow companies of all sizes to automate, streamline and effectively manage the processes required to ensure compliance and get products to market sooner.


MasterControl Industry-Specific Solutions:
MasterControl Clinical Quality (GCP) JumpStart
MasterControl DHF JumpStart
MasterControl DIA Reference Model EDM JumpStart
MasterControl DIA Reference Model TMF JumpStart
MasterControl GLP JumpStart
MasterControl GMP JumpStart"
MasterControl Pharma R&D JumpStart
MasterControl Submissions Gateway
MasterControl Submissions Locker
MasterControl Submissions Ready

MasterControl Clinical Quality (GCP) JumpStart™

MasterControl Clinical Quality (GCP) JumpStart provides a complete document management solution for all clinical quality document needs. It is a preconfigured document management tool for clinical quality research areas who wish to implement a solution to create, edit, revise, approve, access and train on good clinical practice (GCP) to support and ensure quality compliance of day-to-day operations in their clinical research activities.

MasterControl DHF JumpStart™

MasterControl DHF JumpStart is a tool that bridges the gap between design and manufacturing and provides project management, design control processes, and document control and approval. It's a preconfigured database that helps small- to medium-sized device companies quickly organize their work so they spend less time with administrative duties and more time in development.

MasterControl DIA Reference Model EDM JumpStart™

MasterControl Reference Model — EDM JumpStart provides an industry best practice configuration to facilitate better management of regulatory submission documents and correspondence received from agencies. The flexible model boosts efficiency and provides enterprise-level functionality.

MasterControl DIA Reference Model TMF JumpStart™

MasterControl has developed the MasterControl DIA Reference Model — TMF Jumpstart best practices configuration to facilitate management of the thousands of clinical documents generated throughout a clinical trial. This model consists of standardized taxonomy and metadata and it clearly defines and outlines the organization of TMF content using standard nomenclature.

MasterControl GLP JumpStart™

MasterControl Good Laboratory Practice (GLP) Jumpstart provides an organization with a complete document management solution for all its non-clinical quality document needs. It is a preconfigured document management tool for nonclinical laboratories who wish to implement a solution to create, edit, revise, approve, access and train on good laboratory practice (GLP) to support and ensure quality compliance of day to day activities in their laboratories.

MasterControl GMP JumpStart™

MasterControl GMP JumpStart provides life science manufacturers with tools that facilitate the organizational processes and conditions under which manufacturing activities are planned, performed, monitored, recorded, archived, and reported. It is a preconfigured document management solution for manufacturers of product, substance and excipients of pharmaceutical and biological products who wish to implement a solution to create, edit, revise, approve, access and train on good manufacturing practice (GMP) documentation to support and ensure quality compliance of day-to-day activities of their manufacturing procedures.

MasterControl Pharma R&D JumpStart™

MasterControl Pharma R&D JumpStart is a best-practice document management configuration for eCTD regulatory submissions and clinical Trial Master Files (TMF) based on the Drug Information Association (DIA) Electronic Document Management (EDM) TMF Reference Model. It is a utopian system specifically preconfigured for pharmaceutical companies' document and project management needs.

MasterControl Submissions Gateway™

MasterControl Submissions Gateway facilitates electronic delivery of FDA applications (such as IND, NDA, and BLA) by providing control in assembling and tracking necessary documentation. It provides appropriate templates to streamline the dossier-creation process. MasterControl can be integrated with leading e-submission applications, connecting approved documents and forms-based content with the dossier assembly process, to accelerate submissions.

MasterControl Submissions Locker™

MasterControl Submissions Locker MasterControl Submissions Locker is an indispensable tool that can be utilized throughout a submission's lifecycle.

MasterControl Submissions Ready™

MasterControl Submissions Ready allows organizations to accelerate the preparation and organization of submissions documents utilizing FDA- and ICH-compliant submissions templates in combination with MasterControl's unrivaled document management solution.

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Download Free Resources
Product Data Sheet: MasterControl JumpStarts and Reference Models Overview
Product Data Sheet: MasterControl Clinical Quality (GCP) JumpStart
Product Data Sheet: MasterControl DHF JumpStart
Product Data Sheet: MasterControl Reference Model™ - TMF Jumpstart
Product Data Sheet: MasterControl GMP JumpStart
Product Data Sheet: MasterControl Pharma R&D JumpStart
Product Data Sheet: MasterControl Organizer Gateway™
Product Data Sheet: MasterControl Submissions Locker™
Product Data Sheet: MasterControl Submissions Ready™