Most CEOs and top managers just don’t get it when it comes to ISO 9001 and all the derivative standards. Th...
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 2 of this 10-part series, SVP of Strategic Growth Brian Curran and Principal Product Management Director
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 1 of this 10-part series, Vice President of Product Rajesh Talpade and Principal Product Management Direc
MasterControl has an unparalleled electronic quality management system (QMS) that helps you turn compliance into a competitive advantage. The MasterControl system has five modules that work together t
Learn about quality in the modern era. A QMS must promote flexibility and responsiveness. By being configurable, risk-based, fast, and customizable, your quality management system can be ready...
Relieve the friction between quality assurance and your manufacturing teams with the help of digital production records found in MasterControl Manufacturing Excellence™. Read the brief...
MasterControl Product Management Director Sue Marchant explains the problems that stand in the way of data-centric quality and how companies can overcome them.
Many hands make light work, as the old saying goes. For businesses facing the pressure of accelerating timelines, the increasing complexity of products and a host of other challenges in modern li
Cochlear helps people hear and be heard by providing high-quality devices. They use MasterControl to ensure quality across the organization.
Ken Peterson, quality and compliance consulting partner of MasterControl and president of Touchstone Enterprises, discusses the processes that inspectors need to follow to find solutions.
In a new case study video, EpiBone, a Brooklyn-based regenerative medicine company developing living grafts for skeletal reconstruction, explains how it is leveraging MasterControl's QMS and manufactu
The book explores how the use of technology in the past decade has helped both regulated companies and regulatory agencies in easing the pains and costs of compliance.
In a regulated environment, the document control process can either be an obstacle course replete with pitfalls, or it can be a smooth ride to a successful product launch.
As a medical marijuana startup or small business you have big ambitions and little margin for error. A digital QMS technology is a driver for getting products ready to go and on the market sooner.
In industries like medical device, biotech and medical marijuana, the margin between success and failure is thin. Master compliance early on to get ahead of your competition.
Creating solutions when traditional problem solving and investigations may not work—or when an improvement or breakthrough is needed beyond a traditional CAPA approach—may be more art than science.
Both FDA inspectors and ISO auditors consider the practices and processes that comprise a corrective and preventive action (CAPA) program to be singularly critical to compliance.