With the template for Pharmacovigilance, you will be able to monitor curated sources with the aim to automate the surveillance of your own products, competitor products, and literature within externally published content.
Monitor a vast numbers of databases, clinical trials data, adverse events, publications, and social media.
Enhance your Pharmacovigilance process
By monitoring with a purpose to fetch upcoming and potential changes within regulatory, compliance and legal on your markets, you ensure proactive decision-making regarding research and development of products and that you comply with regulations and adopt to changes in local and regional laws
Monitor Health Authorities, Industry organizations and forums to stay updated on the latest updates and changes.
Keep track of regulatory
changes and updates
With a content monitoring project where the template for Content Marketing & Writing is used, you will get a constant inflow of external content that will suit your needs as background material for creation of own content.
Monitor industry media, social media and data bases for literature and technology & trends insights.
Boost your marketing with a
constant inflow of good content
Automation starts here
Hoodin for Pharma
Hoodin for Pharma is an automated solution for Regulatory professionals, QA/RA managers, Pharmacovigilance experts, marketers and writers that need insights, changes, and updates from relevant sources. Easy, smart, and efficient.
Marketing & Writing
and unique values
All the monitoring project templates for Pharma are verified by and designed together with experienced industry experts. With this experience designed into the platform you will be able to:
Monitor the most important and relevant source related to your need.
Monitor both own and competitor products.
Export results and insights for use in reports.
Share results and insights with invited peers (free feature).
Keep track of all changes made in your Hoodin project with the included change-log feature.
Solutions that are validated by industry experts.
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
"I can certainly see how this will save me time in my projects from a purely regulatory intelligence point of view, and I am also trialing the platform for a very specific project, which will be of benefit to both me and my clients. This speaks to the versatility of Hoodin’s platform."
Vince Wek, Bluefinch Medical