06/02/2022
Why hello there!
We're back it again with Edition 003 of The Hilltop Pharma Herald!
We’ll be routinely releasing our newspaper highlighting company news and important / interesting stories in the industry via Twitter, Facebook and on LinkedIn.
We're happy to do our part with the to make news easy and digestible!
Sources for this week's article on Medical Devices Regulations:
1. “Guidance: Medical devices: conformity assessment and the UKCA mark” | GOV.UK https://www.gov.uk/guidance/medical-devices-conformity-assessment-and-the-ukca-mark
2. “Medical Devices” | European Medicines Agency (The EMA) https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices
3. “REGULATION (EU) 2017/745 on medical devices” | Eur Lex, access to European Union Law https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32017R0745&from=EN
4. “REGULATION (EU) 2017/746 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU” | Eur Lex, access to European Union Law https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32017R0746&from=EN
It's easy to keep up with Hilltop across the internet!
Twitter: https://lnkd.in/gQwPZRaQ
LinkedIn: https://www.linkedin.com/company/hilltop-pharma-solutions/
And of course you can always learn more about our services, core ethos and more on our official website:
https://lnkd.in/gwg6mTMt