Achieving Regulatory Compliance Through Clinical Evaluation
By Jasmin Hunter, Senior Consultant Clinical evaluation is a process to collect and assess all [...]
Mar
Free Webinar: PMCF Surveys – How to Ensure Success
Date: 16 January 2024 Time: 17:00-18:00 PM CEST | 11:00 AM – 12:00 PM EST | 8:00 [...]
Nov
Nienke Flipsen-Maassen joins Qserve
Our Qserve CRO team is happy to announce that Nienke Flipsen-Maassen has joined them as [...]
Sep
Personal Health Literacy: Demystifying Readability Requirements for SSCPs Intended for Patients
Date: 26 September 2023 Time: 17:00-18:00 PM CEST | 11:00 AM – 12:00 PM EST | 8:00 [...]
Jul
Free Webinar – 25 Years of Sharing Knowledge – Forward Thinking Series – Clinical
Date: 13 June, 2023 Time: 17:00 – 18:00 PM CEST | 11AM – 12 PM [...]
May
“Monitoring of medical device clinical trials” in accordance with ISO14155 and EU MDR
If you are a medical device manufacturer/sponsor starting a clinical trial, you have the obligation [...]
Mar
Free Webinar – what is the impact of the planned MDR extension?
Date: 13 April 2023 Time: 17:00 – 18:00 PM CEST | 11AM – 12 PM [...]
Feb
On Demand Free Webinar – Clinical Submission Strategy Europe and United Kingdom
This webinar will give insight into what are the differences in Clinical trial submissions in [...]
Feb
On Demand Free Webinar – Clinical Submission Strategy Europe and United Kingdom
This webinar will give insight into what are the differences in Clinical trial submissions in [...]
Feb
Clinical Suite | Clinical Surveys
Date: 23 March 2023Time: 16:00 – 18:00 CET / 10 am – 12 pm Eastern [...]
Jan