Clinical Resources

Resources and information for Clinical Industries

  • FDA Fronts Pivotal Life Sciences Trend in 2020

    FDA Fronts Pivotal Life Sciences Trend in 2020

    This publication provides an in-depth look at the FDA’s transformation and addresses how the agency’s initiative will impact manufacturers of regulated products.

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  • 5 Top Medical Device Industry Trends to Plan for in 2020

    5 Top Medical Device Industry Trends to Plan for in 2020

    This whitepaper will look at some of the trends anticipated to make a substantial impact on the medtech sector in 2020 and offers suggestions about how manufacturers can best position themselves...

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  • 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

    Fagron is an international personalized medicine pharmaceutical company that recently started using MasterControl to improve its quality and manufacturing processes.

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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: MasterControl Clinical CAPA1:45

    Demo: MasterControl Clinical CAPA

    MasterControl Clinical Excellence™ offers a comprehensive clinical quality management system (CQMS) that handles every component of clinical trials, including CAPA management.

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  • Demo: MasterControl Clinical Quality Management System1:08

    Demo: MasterControl Clinical Quality Management System

    MasterControl Clinical Quality Management System (CQMS) provides you with the tools you need to manage quality and operations before, during and after your clinical trial.

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  • Demo: MasterControl eTMF Management System1:36

    Demo: MasterControl eTMF Management System

    Managing all the artifacts in a trial master file (TMF) can be a daunting task. Instead of relying on paper, use the MasterControl eTMF Management System to digitize the whole process.

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  • Demo: MasterControl Clinical Supplier Management Software1:33

    Demo: MasterControl Clinical Supplier Management Software

    Managing vendors is difficult when vendor information is on different systems that don’t communicate with each other. MasterControl Clinical Supplier Management Software eliminates those problems.

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  • Demo: MasterControl Clinical Audit Management System1:09

    Demo: MasterControl Clinical Audit Management System

    Using the MasterControl Clinical Audit Management System connects training, site, study and vendor management on the same platform.

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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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