This article provides detailed information on the UKCA marking and how the new UK conformity marking differs from the EU CE marking.
This article focuses on import procedures in Saudi Arabia and what foreign manufacturers need to do to pass customs and sell their goods in the country. It also provides information about the SASO Saber system.
This article provides manufacturers with information on the Moroccan Cم (CMIM) mark and lists some digital sources where they can stay updated with the changes in the local legislation.
This article provides detailed information on the new conformity marking required for products sold on the market in Great Britain.
This article provides brief information on misbranded and adulterated medical devices.
This post contains information on what safety-critical components are and a list of UL standards applicable to various safety-critical parts implemented in the design of electrical equipment.
This article provides information on all FDA’s compliance actions and penalties, including product recalls, disqualification, civil money penalties and seizure.
This article clarifies what the BXM method is and why medical device manufacturers should use it when performing risk management.
Pre-control and positrol are two methods manufacturers need to use to verify the supplier quality process performance. This article provides readers with brief information on each of these methods.
Product liability prevention is about understanding what to do and how to do it to achieve product safety excellence. For that reason, this article provides information on what product liability is and how to prevent it.