Tom Latham shared Ce Marking Consultants
We are able to represent both our local and international clients with the same intensive focus on quality that is eligible for early CE Certification because of the shared, transparent strategy and structure inside our organisation. After
Tom Latham shared Medical Device Regulatory Consulting Services
Explore top-notch medical device regulatory consulting services to ensure compliance and smooth market entry. Our experts navigate complex regulations, streamline approval processes, and enhance product safety. Gain a competitive edge with
Tom Latham shared Medical Device Regulatory Consultants
Manufacturers can benefit from the technical and regulatory guidance and support provided by Regulatory Affairs Consultants. We deliver services in the most responsible manner. Manufacturers of medical products can rely on us for competent
Tom Latham shared FDA 510k Consultants
Premarket approval, establishment registration, or device listing are not what a 510k is. Typically, an FDA 510k is required in three circumstances. A manufacturer or specification developer must show that the medical device is essentially
Tom Latham shared MDR CE Marking
The purpose of the MDR CE Marking is to guarantee a high degree of protection for human health and safety as well as to offer a framework that is conducive to innovation and competitiveness of the European market for medical devices. We are
