EU QPPV Services
Outsourcing of qualified persons responsible for pharmacovigilance in any EU market
What is EU QPPV?
✓ The role of European Union Qualified Person for Pharmacovigilance is key for your entire European pharmacovigilance system.
✓ This is the person responsible for ensuring your PV system and set of pharmacovigilance processes are set up and maintained in accordance with European legislation.
✓ They should be your main contact point between you and the regulatory authorities, most importantly EMA.
What do they oversee?
Under Tepsivo pharmacovigilance system, the EU QPPV oversees and maintains the full delivery of the complete pharmacovigilance solution in Europe, including oversight of the following QPPV responsibilities:
Need a QPPV?
What makes a Tepsivo QPPV special?
Freedom from mundane administrative tasks, and the ability to focus on science
Challenge: Today’s QPPVs became admin workers
The role of EU QPPV is of someone with high level of experience and training in pharmacovigilance, often a Medical Doctor, pharmacist, or another holder of a life sciences degree. In short, highly qualified person, who should spend their time on added-value tasks.
However, it has become standard in the industry for EU QPPVs to spend most of their days worrying about numerous reports, managing people, review endless trackers and overall waste their time on admin activities they shouldn’t really be concerned with. That doesn’t fly with us!
Solution: Fight inefficiency with automation
The role of EU QPPV is of someone with high level of experience and training in pharmacovigilance, often a Medical Doctor, pharmacist, or another holder of a life sciences degree. In short, highly qualified person, who should spend their time on added-value tasks.
However, it has become standard in the industry for EU QPPVs to spend most of their days worrying about numerous reports, managing people, review endless trackers and overall waste their time on admin activities they shouldn’t really be concerned with. That doesn’t fly with us!
Thanks to our streamlined and automated global pharmacovigilance system solution, the EU QPPV has daily real-time access to all activities and data within the PV system they oversee. They don’t need to wait for compiled reports, or talk to some project manager to receive input they would then have to review in several different documents.
Tepsivo Platform
Tepsivo EU QPPVs simply log into our proprietary Tepsivo Platform and see everything for themselves, with the ability to comment directly on any given activity as they see fit.
The legal requirement of access to PSMF as well as oversight of all PV tasks is guaranteed at all times. Tens of admin hours saved each month, and an EU QPPV happier, more effective, and focused on what should matter and what they are trained for.
Read more about our global end-to-end pharmacovigilance system
and how we manage this via our unique Tepsivo Platform.
Do we claim to have the highest,
“above market-level”, qualified QPPVs in the world?
No, such argument makes no sense even as most our competitors try to make it. We’re not here to question the education, training, and qualification of people at other companies, just because they work elsewhere. What we can do, as opposed to everybody else, is to provide a system where the QPPVs can spend their valuable time on things that matter, and not waste it with boring administrative tasks.
You can make your own judgment whether highly experienced people prefer to work in a system imposing massive admin workload on them, or a system in which they can fully focus on things where their expertise brings value.
If you have an inhouse EU QPPV, or actually are an EU QPPV yourself, our system and Tepsivo Platform is definitely the right choice for you! We don’t insist on using our staff to perform the PV activities, our set of processes and tools is what makes us best in the field.
Let’s have a chat
Whatever your needs are, we look forward to getting in touch with you.
Feel free to drop us a message and we will contact you right away.
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