Enhance your Post Market Surveillance
process with Hoodin
With hoodin and the use case template for Post Market Surveillance you may choose a wide or narrow-focused approach, with minimal effort to help reach compliance. Regardless of your choice, you will get the job done in a timely, precise, and automated way
Building blocks for Post Market Surveillance
Hoodin makes it easy for you. The expert-designed template for Post Market Surveillance comes with a number of building blocks called monitoring feeds. You may choose to use only a few of them or all. Every feed comes with recommended sources to monitor.
Some of the available sources for literature search
Databases and sites with scientific papers, reports and journals to follow the ongoing development around your and competitors products
Some of the available sources for unsolicited reports
Monitor niche industry media, blogs, trade journals and social media to detect mentions of your product.
Some of the available sources
Some of the available sources for incident reports
Monitor incident reports on your own and competitors' products. Examples of curated sources to monitor in this monitoring feed is Maude.
Some of the available sources for clinical trials
Keep track of clinical trials databases to get notified if and whenever someone external performs a clinical study with your product.
SOTA Technology & trends
SOTA (State Of The Art) reference monitoring to identify innovations, newly initiated research, patents, etc.
Some of the available sources for SOTA Technology & Trends
SOTA Regulatory potential changes
Some of the available sources for SOTA Regulatory 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 for efficiency
Through Hoodin, you may monitor specific sources and digital services for externally published content. You may also monitor a vast number of databases for literature as well as retrieve signals and fetch content when clinical trial data and adverse events regarding adjacent and or competitive devices and treatments are published.
Save time from manual,
Easy collaboration with colleagues.
Don’t ever miss important insights.
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. Learn more from our client cases and interviews below.
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,