Clinical Resources
Resources and information for Clinical Industries
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MoreFDA 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
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
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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4:06MoreFagron 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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3:10MoreDemo 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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1:26MoreDemo 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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3:15MoreMasterControl 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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1:20MoreDemo 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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1:45MoreDemo: 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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1:08MoreDemo: 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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1:36MoreDemo: 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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1:33MoreDemo: 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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1:09MoreDemo: 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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1:07:09MoreTransitioning 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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6:24MoreHow 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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1:20MoreContract Pharmacal Corporation Successfully Complete FDA Audits with MasterControl EQMS
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MoreTop 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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MoreFDA 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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MoreThe 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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MoreCAP 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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