Clinical Resources
Resources and information for Clinical Industries
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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
When it comes to personalized medicine, quality is paramount. Fagron uses MasterControl for their Quality Management Systems (QMS Software).
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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 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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1:08MoreDemo Introduction: MasterControl Clinical Quality Management System
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1:36MoreDemo Introduction: MasterControl Clinical eTMF Management System
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1:33MoreDemo Introduction: MasterControl Clinical Supplier Management Software
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1:09MoreDemo Introduction: MasterControl Clinical Audit Management System
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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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MoreHow 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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MoreTop 5 Clinical Trends in Pharma and Biologics in 2018
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