“A new era of data protection is beginning.
For medical device companies, compliance must begin promptly in order to comply with the new Data Protection Regulations.
- The European Union’s General Data Protection Regulation (GDPR – 2016/679) was published on April 27, 2016.
- The new European data protection regulation will have a huge impact on medical device companies.
- Coming into force in May 2018, it brings significant changes and new responsibilities to ensure data is kept secure. It means that action must be taken in anticipation of these new regulations
- MedPass, will assist you in the understanding of the new regulations and provide support on your regulatory process.
Companies in and outside the European Union, must commit and invest in this new requirement on order to become compliant with the European regulations. This will both avoid fines and penalties and also ensure that data processing and data transfer in clinical trials are safe and guaranteed.”