Medical device companies seeking to sell product in two or more of the following countries could benefit from adhering to the Medical Device Single Audit Program (MDSAP): -Australia -Brazil -Japan -Canada -United States This webinar offers insights into MDSAP requirements, the program’s members, tips for adherence and specific benefits to industry.
Visualizing a new data-centered quality paradigm. When the first Nokia and Motorola cell phones that were affordable and small enough to fit in your pocket hit the market...
WD-40 Company needed a way to ensure that every drop of product produced by globally diverse contract manufacturing organizations (CMOs) measured up to the company’s unwavering standard of quality.
2:50Cochlear helps people hear and be heard by providing high-quality devices. They use MasterControl to ensure quality across the organization.
Read how MasterControl helped Hu-Friedy ensure compliance with FDA's 21 CFR Part 820 Quality System Regulation (QSR), and ISO 13485.
NAMSA, a leading contract testing laboratory relies on MasterControl to meet rigorous FDA and ISO requirements.
Megadyne Medical Products has a global customer base, which means the medical device organization must comply with the requirements of multiple regulatory agencies.
The Medical Devices Regulation and In Vitro Dianostic Regulation deadlines are fast approaching. Learn the requirements, timelines, and terminology you need to be prepared.
Device history records (DHRs) are the most important artifacts generated in the course of medical device manufacturing, yet many manufacturers still rely on manual, paper-based DHR systems.
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.
Noncompliance among medical device developers typically falls under two areas: design control and document management. These two critical elements intersect in one place: the design history file.
Review the conundrum companies are experiencing if they want to maintain both ISO 9001 and ISO 13485 certification: How to comply with the varied requirements within only one quality system.
The medical device landscape is changing, due in large part to the controversial U.S. excise tax that applies to American-made and imported medical devices.
The Food and Drug Administration (FDA) has established and maintains Part 820- Quality System Regulation (QSR), also known as 21 CFR 820 or 'Current good manufacturing practice' (cGMP).
Examine how obtaining ISO 13485 certification can open doors to untapped domestic and international business opportunities, and obtain recertification to the new revision.
The FDA’s approach to the inspection process of medical device manufacturers, Quality System Inspection Technique (QSIT), embraces a top-down inspection of a firm’s QMS.
When a company’s product development engineers and quality professionals fail to cooperate adequately, the company risks experiencing costly delays and inefficiencies.
