Sustaining Regulatory Compliance While Managing an Adverse Drug Event
Outdated paper based process management methods are messy, to say the least. They also foster inefficiency, disconnected processes, poor reporting systems, and a lack of oversight. If a life science company does happen to come across an adverse drug event, a paper based management method simply won't cut it.
MasterControl™ suite provides the software solution regulated life science companies need to sustain compliance with FDA regulation. When customer complaints, deviations, adverse drug event, and other incidents occur, MasterControl software solutions use automated routing, notification, delivery, escalation, and approval to launch and track all related documents. All of the documents and forms needed to report an adverse drug event to the FDA are easily accessible due to MasterControl's advanced tracking system.
To learn more about making the right decisions when it comes to managing an adverse drug event, visit MasterControl's Education Center to find informative white papers and other valuable resources.
Life Science Industry Education and Collaboration
With an ever-increasing movement towards globalization, the life science industry is becoming more competitive. MasterControl provides the educational and research materials regulated companies need to stay abreast of industry current events, software solutions, and collaborative endeavours.
MasterControl's complimentary monthly newsletter, GxP Lifeline, is aimed at providing life science companies, especially those within the pharmaceutical, biotechnology, medical devices, blood/tissue, and clinical/medical laboratory sectors, with informative and interesting stories and articles. GxP Lifeline also includes a monthly best practice tip and a list of upcoming life science events to help companies make the right decisions about managing an adverse drug event and every other part of their GxP process.
Contact MasterControl Today for Adverse Drug Event Solutions
To learn more about how MasterControl suite provides solutions for automating, streamlining, and effectively managing every step of the product development cycle, including the possibility of an adverse drug event, contact MasterControl online or call toll free at 1.800.825.9117 to speak with a representative.