Regulatory Rapporteur April 2018 | MEMBERS |
Companion diagnostics: Requirements under the new IVD Regulations | MEMBERS |
Exploring the impact of clinical trial transparency – Part 1: Disclosure issues | MEMBERS |
Interview: Big strides in the devices sector | MEMBERS |
ISO 13485 versus ISO 9001 – Converging or diverging? | MEMBERS |
Human factors and usability engineering: MHRA guidance for devices and combinati | MEMBERS |