How did you decide to participate in the Biomapas Academy?

When I used to walk past a pharmacy every day, I could never stop dreaming about being able to help people and develop innovative pharmaceuticals. So while studying biomedical sciences, I became interested in the drug development paths, which led me to medicinal chemistry. And one day at the university, I saw a poster about the Biomapas Academy, which could help me understand what, how, where, and when happens to pharmaceutical products during the whole journey to reach us, so I signed up for it without hesitation. Even though I am usually not a lucky person, I was selected to be one of the participants, which surprised me!

How was your experience regarding the Academy?

During the few months, I deepened my existing knowledge of drug development stages and expanded it to learn more about drug regulation and pharmacovigilance. After graduating from the Academy, I got the opportunity to try out regulatory affairs as part of Biomapas – I completed a summer internship in the Regulatory Affairs department.

 

How do you feel after graduating from the Academy?

I will never forget this practice in my life, not only because it fulfilled what I was looking for, but it let me realize that I want to return to this company after my graduation and put my accumulated knowledge to use. Thanks again to all Biomapas staff for their insights and advice, and I hope to see you soon.

Biomapas Academy

What is Clinical Research? Regulatory Affairs? Pharmacovigilance?

How Do Early Phase Oncology Trials Evolve?

How Do Early Phase Oncology Trials Evolve?

In the last few years, a major breakthrough in cancer research has occurred: early phase oncology trials. This type of trial is designed to test whether a new drug has any adverse effects on people and also provides anecdotal evidence that it might be efficacious....

read more
Running A Clinical Trial In Georgia

Running A Clinical Trial In Georgia

Moving Clinical Trials away from Ukraine and Russia Russia, Ukraine, and other CIS countries have been significant contributors to clinical trials in many therapeutic areas for several years. With access to experienced investigators, good quality, and large patient...

read more
Running A Clinical Trial In Kazakstan

Running A Clinical Trial In Kazakstan

Moving Clinical Trials away from Ukraine and Russia For a long time, Russia, Ukraine and other countries in the Commonwealth of Independent States (CIS) have been the host of ample clinical trials in various therapeutic areas. And for a good reason: countries in the...

read more

A guide to a splendid internship experience

An internship is a great start to your career. You gain experience in various fields, get in touch with various professionals from different departments and have a mentor leading you down the road. It’s a great opportunity to see how the processes work inside the...

read more

5 tips to have a great internship interview

We can all agree that a first impression is essential. The same general rule applies to your internship or a job interview with any company. Your interview is the first step into that company and its culture. We all want to leave a good or even a great impression of...

read more
Pharmacovigilance in the MENA Region

Pharmacovigilance in the MENA Region

This blog focuses on pharmacovigilance (PV) in the MENA Region; the Middle East and North Africa. We do this by comparing the MENA region and Europe and inter-country differences in the MENA region. Local legislation and requirements will be discussed, such as...

read more

How to prepare an eye-catching resume?

Everything has a start, right? Well, the start of your career can become a good and professional resume, or sometimes better known as a CV, Curriculum vitae. It’s often one of the first things recruiters look at when you are applying for a job or an internship. In...

read more

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information