How did you decide to participate in the Biomapas Academy?
The first thing that caught my attention was the Biomapas Academy poster hanging on my university’s bulletin board. Shortly afterwards, the faculty management shared Biomapas’ invitation to register for the first Biomapas Academy. I wanted to learn more about this company, so I decided to take my chances and apply to the Academy. I was thrilled when I received a call with the happy news that I had successfully passed the selection process and was invited to attend the Academy.
What was your experience during the three months?
I listened to many interesting lectures, during which we got to know the company and its areas of activity. We listened to lectures on clinical trials and their organization, pharmacovigilance, regulatory affairs, bioethics, drug registration, and more. I believe that the knowledge gained at the Academy is valuable and helpful for all participants of the Academy and their future careers.
What did the future hold for you after the Academy?
I mainly was interested in pharmacovigilance, so we agreed on an internship in this department during the summer. Interesting fact: the first Biomapas poster I saw was about pharmacovigilance! And the best thing is that after the internship, I was able to join and become a part of this great team. I am happy to be here and to learn from real professionals in this field.
What would you say to the future participants?
I want to encourage everyone who is thinking about participating in the Biomapas Academy. Being at the Academy is exciting and worthwhile. By joining the Academy, you will broaden your horizons, learn from global professionals, improve your life sciences knowledge, and gain valuable experience. I wish good luck to all participants. See you soon at Biomapas!
Biomapas Academy
What is Clinical Research? Regulatory Affairs? Pharmacovigilance?
Unlock Trial Success with the FSP Hybrid Model
Learn how the FSP hybrid model combines the best of FSO and FSP in clinical trials, enhancing operational control and flexibility.
Breaking silos across Medical Information & Pharmacovigilance
Discover solutions for effective PV & MI data management, including handling Adverse Events, Product Quality Complaints, and MI inquiries. Our experts will walk you through real-life examples and hands-on solutions.
Unlocking Success. The FSP Advantage in Clinical Research
FSP is a rising trend in clinical research, expected to gain further prominence due to its cost-effectiveness and demand for specialised expertise. Our FSP model offers benefits such as cost savings, expert advice, flexibility, and risk mitigation. Let’s discuss how...
Affiliate Based Outsourcing Model for Regulatory Affairs.
Affiliate based Outsourcing Model for Regulatory Affairs works as a replacement or an extension of the company’s internal and local RA resources. Many challenges come up from managing your RA activities as sometimes their processes are not harmonized across different...
Regulatory Outsourcing in the CEE Region
In this informative session we decode the intricate landscape of regulatory affairs outsourcing in the CEE region and provide practical, implementable strategies to optimize and maximize your operations and outsourcing strategies.Let’s discuss how we can streamline...
Regulatory Framework of Drugs in MENA: Insights
In this webinar, our experts discuss regulatory affairs of medicinal products. Two aspects that have recently gained increasing importance among the various stakeholders, namely the eCTD implementation across the region and the serialization and barcoding requirements...
How to Set Up and Manage Local Pharmacovigilance Networks for Global Compliance
Structure compliant local PV networks while maintaining centralized oversight, from regulatory obligations, partner selection, QPPV responsibilities, technology integration and outsourcing within a scalable strategy.
How medical writing supports every stage of the drug’s lifecycle
Discover how medical writing for clinical trials supports each phase of drug development with essential documentation.
Unlock the full potential of your medical writing outsourcing
When clinical timelines are tight and regulatory expectations keep shifting, outsourced medical writing becomes a competitive edge. The right medical writing CRO can help you scale document production, stay aligned with evolving compliance standards, and bring your...
Exploring Regulatory, Inspection, and Cultural PV Trends in APAC
Explore evolving APAC PV trends: cultural diversity, CBDT rules, inspections, RMPs, outsourcing, and vendor audit best practices.
