Post Market Surveillance process
With the use case template for Post Market Surveillance you will be able to monitor curated sources with the aim to automate your surveillance of your own products, competitions products and literature within externally published content.
Monitor externally published content
Hoodin makes it easy for you. To simplify the task to set up proper surveillance, the Hoodin use case template for PMS consists of pre-designed and recommended monitoring feeds with associated sources per monitoring feed.
Databases and sites with scientific papers, reports and journals to follow the ongoing development around your and competitors products
Monitor niche industry media, blogs, trade journals and social media to detect mentions of your product.
SOTA Technology & trends
SOTA (State Of The Art) reference monitoring to identify innovations, newly initiated researches, patents, etc.
Monitor incident reports on your own and competitors' products. Examples of curated sources to monitor in this monitoring feed is Maude.
Keep track of clinical trials databases to get notified if and whenever someone external performs a clinical study upon your product.
SOTA Regulatory potential changes
SOTA (State Of The Art) reference monitoring to identify potential changes in regulations and laws. Such as national and regional prohibition of chemicals, products and methods.
Automation is key
Through Hoodin, you may monitor specific sources and digital services (social media) for externally published content (unsolicited reporting and feedback). You may also monitor a vast number of databases for literature as well as retrieve signals and fetch content when clinical trials data and adverse events regarding adjacent and or competitive devices and treatments are published.
Save time from manual,
Don’t ever miss important insights.
Easy collaboration with colleagues.
Create your own knowledge hub with relevant content.
Some of our customers & partners
By using Hoodin, our customers and partners are saving up to 90% time from manual, repeated searches. Take part in client cases and interview below to learn more.
We want to be proactive as a company
Syntach was well aware of the enormous amount of information available online and therefore wanted to find a way to streamline and automate external monitoring and prepare for the upcoming requirements for Post Market Surveillance and the regulations regarding MDR (Medical Device Regulation).
"Now we can coordinate the work in a better way by having one place for this that everyone has access to. We no longer have to risk doing the job twice.”
Victoria Krüger, Chief of RA/QA
Post market surveillence
"When you explore Hoodin you're surprised how their automation delivers beyond your expectations as you find real-time surveillance is quick to set up and the reporting quick to do.
Hoodin has delivered on what seemed like the impossible data automation solution for MedTech, so my expectation for future collaboration and the innovation output is very high."
Jacqueline van Druten,