Biomapas Logo

Insights & Resources For Life Sciences Professionals.

Whether you’re a healthcare professional, a researcher, or simply interested in the drug development, you’ll find valuable information and resources here that can help you stay informed and make informed decisions. Let us know what else you’d like to hear about!

Pharmacovigilance & Medical Information
Clinical Research
Regulatory Affairs
How to set up a pharmacovigilance system?

How to set up a pharmacovigilance system?

Nov 30, 2022

Webinar: Setting up a pharmacovigilance system in Europe. Where to start? What to consider? Setting up a pharmacovigilance system is not as straightforward an answer as it may sound. There are many aspects to consider, which can seem complicated, especially when you must focus on developing your...

The Role of Regulatory Intelligence in Pharmacovigilance

The Role of Regulatory Intelligence in Pharmacovigilance

Nov 25, 2022

Regulatory Intelligence is a reliable and invaluable tool when it comes to pharmacovigilance. It's so important because it allows companies to remain up-to-date with the most recent drug safety data and identify new information quickly. What Is Regulatory Intelligence? Regulatory Intelligence is...

Role of the Local Person for Pharmacovigilance (LPPV)

Role of the Local Person for Pharmacovigilance (LPPV)

Nov 11, 2022

The EU changes on the regulatory side have been significant. It has not only seen pharma companies face a new challenge to meet the requirements but also regulated medicinal products manufacturers, distributors and Pharmacovigilance professionals. The Local Person for Pharmacovigilance (LPPV) is...

All You Need To Know About Pharmacovigilance

All You Need To Know About Pharmacovigilance

Aug 22, 2022

Pharmacovigilance is the process of monitoring the safety and effectiveness of medications. The term was introduced in the early 1970s and evolved to include a broader range of activities. It's vital to ensure that patients have access to safe and effective drugs and that manufacturers make the...

Artificial Intelligence in Pharmacovigilance

Artificial Intelligence in Pharmacovigilance

Jul 7, 2022

Automation & AI in Pharmacovigilance: Promises and Realistic Expectations Recent years have seen increasing pharmaceutical companies' pharmacovigilance (PV)-related activities. The promise of artificial intelligence (AI) and automation is often mentioned as a way to meet the increasing PV...

Pharmacovigilance Opportunities in the MENA Region

Pharmacovigilance Opportunities in the MENA Region

Jun 1, 2022

Webinar: Pharmacovigilance Opportunities in the MENA Region Pharmacovigilance is getting more and more attention in MENA countries thanks to new regulations and steps in the right direction. The MENA region itself holds great promise for the pharmaceutical industry, being potentially hugely...

Selecting A CRO For An Early Phase Oncology Trial

Selecting A CRO For An Early Phase Oncology Trial

Sep 5, 2022

As oncology drug developers, you likely know that selecting the proper Contract Research Organization (CRO) for your Phase 1 clinical trial is a crucial step in bringing your treatment to the market. This article provides insights for oncology drug developers when selecting a CRO for an Early...

How Do Early Phase Oncology Trials Evolve?

How Do Early Phase Oncology Trials Evolve?

Aug 8, 2022

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. This blog post will discuss the...

Running A Clinical Trial In Georgia

Running A Clinical Trial In Georgia

Jul 23, 2022

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 populations, we could often...

Running A Clinical Trial In Kazakstan

Running A Clinical Trial In Kazakstan

Jul 16, 2022

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 region provide access to large...

How to Avoid Delays in Your Early Phase Oncology Trial?

How to Avoid Delays in Your Early Phase Oncology Trial?

Jun 10, 2022

Webinar: How to Avoid Delays in Your Early Phase Oncology Trial? Many things can go array in your early phase oncology trials, from protocol development, taking care of a safety profile, getting the ethics committee / regulatory authority’s approval, managing vendors, and much more. They all cost...

Q&A. How does the conflict between UA & RU impact the pharma industry?

Q&A. How does the conflict between UA & RU impact the pharma industry?

Mar 25, 2022

Webinar: How does the conflict between UA & RU impact the pharma industry? Like the rest of the world, the pharmaceutical and biotech industries are beginning to worry about their ability to continue operations. And with good reason. Russia's invasion of Ukraine affects millions of people, not...

Must-Know Legislation for Medical Device Registration in the EAEU

Must-Know Legislation for Medical Device Registration in the EAEU

Jun 17, 2021

EAEU legislation for Medical Device registration has been continuously updating for the last six years since the Eurasian Economic Union, otherwise known as EAEU, was entered into force in 2015. Five countries have signed the "Treaty on the Eurasian Economic Union" to create a single regional...

Biosimilars in the MENA Region: Regulatory Landscape

Biosimilars in the MENA Region: Regulatory Landscape

Apr 27, 2021

Regulatory affairs for biosimilars in Middle East North Africa (MENA) region are evolving as existing guidelines and regulatory frameworks are being updated. Since European Medicines Agency (EMA) introduced a legal pathway for biosimilars approval in 2004, several global agencies, e.g., WHO, MHRA,...

Successful Medical Device Registration in EAEU: New Legislation (Part 1)

Successful Medical Device Registration in EAEU: New Legislation (Part 1)

Apr 2, 2021

Webinar: Successful Medical Device Registration in EAEU: New Legislation (Part 1) The webinar discusses and explains the basic, essential, and theoretical matters of the EAEU system, outlines the new approach to the quality, safety, and efficacy assessments, and compares the EAEU system, current...

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.
Affiliate-Based Outsourcing
CSV For Pharmacovigilance Systems
Early Phase Oncology
Functional Service Provision
M&A Support

Clinical Research

Read more

Regulatory Affairs

Read more

Pharmacovigilance

Read more

Medical Information

Read more