Clinical Pharmacovigilance

Clinical pharmacovigilance

PV no longer a hurdle for your smooth clinical study

Running a clinical trial study

is often pain in and of itself.

Every bit of administrative overhead and complexity make the task and budget ever more daunting.

We make sure pharmacovigilance requirements won’t stand in the way of successfully managing your clinical studies.

Laptop screen showing Tepsivo Platform interface

Tepsivo clinical PV solution allows you to effectively run your clinical trials.

With our highly automated system, part of a comprehensive Tepsivo OnePV solution, you can sleep easy – your pharmacovigilance obligations are well taken care of while your costs stay low.

Processing SAEs or SUSARs

does not need to be a soul-drenching activity

With its built-in case intake module, aggregate reporting and Tepsivo Safety Database, Tepsivo OnePV can take care of the full process with little human touch from A to Z.

100%

PV processes integrated in one system

0

administrative overhead or needless “PM meetings”

2

weeks to implement the full solution

Data under full control

and in the right format

investigators report directly into Tepsivo OnePV
file-to-text automatic transcriptions
easy and direct reporting to FDA, EMA, MHRA and other authorities around the globe
automated DSURs or other aggregate reports

End-to-end

Outsourced clinical process

Global

150+ countries covered

Software & Service

Combined in one unique solution

Focus on science

and value-added activities

By automating away and eliminating needless mundane tasks, we have no need to engage people for low-level administrative tasks and looking for lowest costs to be economical.

As a result, our pharmacovigilance team consists of highly qualified experts who focus their time where it should be spent – solely on activities with real impact on patient safety.

Tepsivo

OnePV

Clinical PV service is driven by Tepsivo OnePV and the fully integrated pharmacovigilance system, world’s only completely digital inhouse solution.

Tepsivo

OnePV

Clinical PV service is driven by Tepsivo OnePV and the fully integrated pharmacovigilance system, world’s only completely digital inhouse solution.

A single solution

for your PV needs

With Tepsivo OnePV utilized completely for a post-marketing pharmacovigilance system, your transition into approval marketing stages can be seamless through one system.

You can also run clinical studies in parallel with your existing marketing PV requirements, all managed completely by Tepsivo and Tepsivo OnePV.

1 provider

with inhouse software and full service

100% compliance

at the lowest possible cost

1 provider

with inhouse software and full service

100% compliance

at the lowest possible cost

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.

Book a 15-minute consultation for FREE

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