About the Journal for Medical Device Regulatory Affairs
The Journal of Medical Device Regulation is intended to educate, provide professional guidance, develop core competence of regulatory professionals, and promote debate on fundamental and topical matters within the medical device industry. In addition to publishing medical device regulatory affairs review and discussion articles by opinion leaders from the device community, the Journal summarises the news headlines from around the world and provides useful reference information in the form of charts and briefing documents.
The Journal is a quarterly, subscription-only publication which is currently only available in electronic format. The primary language of the medical device regulatory affairs Journal is English but abstracts of key articles are provided in a number of other languages. Feature articles in other primary European languages will also be included from time to time.
Why should you read it?
The Journal of Medical Device Regulation helps you:
- keep your knowledge of international medical device regulatory and compliance issues up-to-date
- monitor worldwide regulatory developments in one easy step
- understand the significance of new legislation and how to apply it correctly
- quickly find essential information vital to your company’s regulatory operations
- build up a comprehensive resource of medical device regulatory affairs and compliance information within your company
Who should read it?
The Journal of Medical Device Regulation is an essential reference for:
- regulatory personnel in medical device companies
- Competent Authorities
- Notified Bodies
- medical device regulatory affairs and compliance consultancies
- patent agents
- research associates
What does the Journal include?
Each issue of the Journal of Medical Device Regulation contains:
- review and discussion articles by opinion leaders from the medical device industry
- factual summaries of legislative changes from around the world
- guidance on the interpretation and impact of current medical device regulatory and compliance issues
- useful, easy-to-use reference information in the form of charts and briefing documents
- abstracts of key articles in a number of languages