Clinical Resources

Resources and information for Clinical Industries

  • The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future

    The Evolution of Medical Device Clinical Trials: Their Background and a Look Toward the Future

    Knowledge of regulatory requirements and the application of rigorous clinical investigation processes can help companies accelerate the time it takes to bring new devices to the market.

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  • Fagron Uses MasterControl's Quality Management for their Personalized Medicine4:06

    Fagron Uses MasterControl's Quality Management for their Personalized Medicine

    When it comes to personalized medicine, quality is paramount. Fagron uses MasterControl for their Quality Management Systems (QMS Software).

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  • Demo Introduction: MasterControl eTMF Software Systems3:10

    Demo Introduction: MasterControl eTMF Software Systems

    Learn about MasterControl's eTMF product and how it can help your business. Learn more about eTMF Software Systems and more: https://www.mastercontrol.com/clinical/etmf-software-systems/

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  • Demo Introduction: MasterControl eTMF Software Systems1:26

    Demo Introduction: MasterControl eTMF Software Systems

    Learn about MasterControl's eTMF product and how it can help your business. Learn more about eTMF Software Systems and more: https://www.mastercontrol.com/clinical/etmf-software-systems/

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  • MasterControl eTMF Manager3:15

    MasterControl eTMF Manager

    See how MasterControl’s eTMF Manager software solution enables real-time visibility into the status of all clinical study activities and trial master file artifacts.

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  • Demo Introduction: MasterControl Clinical Studies1:20

    Demo Introduction: MasterControl Clinical Studies

    Efficiently manage all clinical study information, including Trial Master Files (TMF) and data from participating study sites and clinical vendors supporting a study.

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  • Demo Introduction: MasterControl Clinical CAPA1:45

    Demo Introduction: MasterControl Clinical CAPA

    See how MasterControl helps organizations efficiently manage clinical quality processes like clinical CAPA, site monitoring, issue management, and deviation management.

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  • Demo Introduction: MasterControl Clinical Quality Management System1:08

    Demo Introduction: MasterControl Clinical Quality Management System

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  • Demo Introduction: MasterControl Clinical eTMF Management System1:36

    Demo Introduction: MasterControl Clinical eTMF Management System

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  • Demo Introduction: MasterControl Clinical Supplier Management Software1:33

    Demo Introduction: MasterControl Clinical Supplier Management Software

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  • Demo Introduction: MasterControl Clinical Audit Management System1:09

    Demo Introduction: MasterControl Clinical Audit Management System

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  • Transitioning from the Medical Device Directives (MDD) to the Medical Device Regulation (MDR)1:07:09

    Transitioning from the Medical Device Directives (MDD) to the Medical Device Regulation (MDR)

    In this video, Linda Chatwin, Esq., RAC from UL explains how to prepare for the transition from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR).

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  • How MasterControl’s Training Management Software Helps the Institute for Transfusion Medicine6:24

    How MasterControl’s Training Management Software Helps the Institute for Transfusion Medicine

    In this customer testimonial, system administrator Patrick Farley discusses how MasterControl’s Training module has enabled the Institute for Transfusion Medicine (ITxM) to successfully complete 750,0

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  • Contract Pharmacal Corporation Successfully Complete FDA Audits with MasterControl EQMS1:20

    Contract Pharmacal Corporation Successfully Complete FDA Audits with MasterControl EQMS

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  • Top 5 Clinical Trends in the Medical Device Industry in 2018

    Top 5 Clinical Trends in the Medical Device Industry in 2018

    This white paper provides the inside scoop on the five trends currently making the most waves in the clinical research area of the medical device sector.

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  • FDA Guidance for Clinical Investigators, Sponsors and IRBs Regarding Adverse Event Reporting in GCP Regulated Environments

    FDA Guidance for Clinical Investigators, Sponsors and IRBs Regarding Adverse Event Reporting in GCP Regulated Environments

    This white paper examines the key points of the guidance and the thinking behind the FDA’s 2009 “Guidance for Clinical Investigators, Sponsors and IRBs”

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  • The Top 5 Benefits of Electronic GLP Audit Management

    The Top 5 Benefits of Electronic GLP Audit Management

    This white paper discusses common audit-related challenges faced by non-clinical research laboratories that still use a paper-based quality system.

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  • CAP Accreditation and Document Control

    CAP Accreditation and Document Control

    The College of American Pathologists (CAP) outlines the requirements and benefits of CAP accreditation for clinical laboratories.

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  • How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance

    How to Use Risk-Based Monitoring and Clinical CAPA to Ensure Compliance

    Given the enormous cost, time, and effort involved in clinical research, sponsors and CROs need to mitigate risks and ensure compliance during development to be able to launch their products.

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  • Top 5 Clinical Trends in Pharma and Biologics in 2018

    Top 5 Clinical Trends in Pharma and Biologics in 2018

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