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Pharmacovigilance. How to simplify the work?

16.03.2021

Pharmacovigilance. How to simplify the work?

 

Have you ever thought about the meaning of the word “simplify”?

Is it about reducing the amount of work?

 

We at OtiPharm Data Pro have long been looking for an answer to the question of how to make the work of a pharmacovigilance expert, QPPV, medical director easy, without abusing excessive simplification.

 

And we found a solution: take away the routine and highlight only the important.

 

It is the monotonous, stereotypical work that causes the most feelings of fatigue and boredom.

 

In our work, we have focused on those aspects of pharmacovigilance that are time consuming and often repeated:

– Search for the drug, instructions, report in various folders and documents;

– Regular search in the literature on side effects of the drug and data download;

– The need to physically send paper reports to the regulator;

– The need to control whether subordinates or colleagues have entered and saved data on drugs;

– The need to weed out a lot of irrelevant information in the search process.

Our specialist has expertise, understands the intricacies and features of the procedure of pharmacovigilance, seeks to work at the expense of his intelligence, rather than perform mechanical work. It is for him that we have created a digital pharmacovigilance platform. Thanks to her, the work of a specialist turns into an interesting expert and intellectual activity.

What do experts value most about us?

First, a user-friendly interface.

Everything important is at hand, unnecessary information is not distracting. All steps to find and pull up information about the drug are calculated, simplified, honed.

 

 

Second, you don’t have to wait for an expert to be at work to solve an urgent task or problem. Access to information about the drug, instructions, side effects, etc. is available 24/7 from various gadgets, including from the phone.

Second, you don’t have to wait for an expert to be at work to solve an urgent task or problem. Access to information about the drug, instructions, side effects, etc. is available 24/7 from various gadgets, including from the phone.

 

 

Third, there is no need to sort “garbage information”.

Automated literature search allows you to select only valid sources of information, sort them by drug and date, and then automatically upload to the system.

 

 

Fourth, there is no daily need to generate long reports and then look for a convenient way to send them to the regulator. The OtiPharm Data Pro digital platform includes built-in excel document templates that are easy to fill out and submit to the controller via electronic exchange at the touch of a few keys on your computer.

 

Fifth, everyone understands what they are doing and does not worry about distortion or unauthorized alteration of data in the system, because the OtiPharm Data Pro platform uses “digital footprint” technology, which captures all system changes and identifies the user who made them.

We can list the sixth and seventh. But we are afraid of not having time for changes, additions and updates to our system, which changes daily, the efforts of our developers and our customers, because we get the best ideas for improvement from them.

 

We hope to start implementing your ideas and suggestions soon.

 

 

Click on the link https://bit.ly/3rWRWlv  and order more detailed information about the platform’s features that will be useful to you.