Insights & Resources
For Life Sciences Professionals.
Whether you’re a healthcare professional, a researcher, or simply interested in 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!
Featured Insights
The Perfect Match: How Mid-Sized CRO–Site Network Partnerships Drive Clinical Trial Success – Watch the Recording
How medical writing supports every stage of the drug’s lifecycle
Discover how clinical research and medical writing intertwine across all phases of drug development, from drafting early trial documents to post-marketing activities.
Harmonizing Product Information Across Baltic Markets
In this case study, we share how one of our partner companies successfully harmonized their SmPC, PIL, and labelling across the Baltic region, working with our medical writing experts.
Topic
How can a CRO support Mergers & Acquisition
The role of Contract Research Organizations (CROs) in supporting mergers and acquisitions (M&As) is not a new ...
Clinical Trial Design For Early Phase Oncology Studies
Designing effective early-phase oncology trials is a complex and challenging task, requiring careful consideration ...
Oncology Study Design
Join us for a must-attend webinar on "Exploring Oncology Clinical Trial Design", where expert speakers will share the latest insights.
Setting Up Medical Information In Europe
Setting up a Medical Information Scientific Service
The world of healthcare is constantly evolving, and one of the ...
National Differences in Pharmacovigilance Requirements in Europe
Pharmacovigilance requirements in Europe are primarily governed by the European Medicines Agency (EMA) through the ...
A History of Pharmacovigilance
Pharmacovigilance, also known as drug safety surveillance, is the process of monitoring, identifying, and ...
Developing a Safety Management Plan (SMP) for Pharmacovigilance
Developing a Safety Management Plan (SMP)
What is the Safety Management Plan (SMP)? This article explores all you ...
EMA & FDA: What Are the Similarities & Differences in Risk Management Procedures?
European Medicines Agency (EMA) and Food and Drug Administration (FDA) are regulatory bodies working in Europe and ...
Oncology trials in a shifting economical and geopolitical landscape
The pharmaceutical and biotech fields are spinning around, seeking to adapt to the current geopolitical situation ...
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 ...
The Role of Regulatory Intelligence in Pharmacovigilance
Regulatory Intelligence is a reliable and invaluable tool when it comes to pharmacovigilance. It's so important ...
Role of the Local Person for Pharmacovigilance (LPPV)
The EU changes on the regulatory side have been significant. It has not only seen pharma companies face a new ...
Running Clinical Trials in Eastern Europe
It has become common practice for pharmaceutical companies to run clinical trials in Eastern Europe. However, it ...
All You Need To Know About Clinical Trials
So you want to improve your Clinical Trial expertise? Great! This field is snowballing and offers many ...
Selecting A CRO For An Early Phase Oncology Trial
As oncology drug developers, you likely know that selecting the proper Contract Research Organization (CRO) for ...
All You Need To Know About Pharmacovigilance
Pharmacovigilance is the process of monitoring the safety and effectiveness of medications. The term was ...
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 ...
Running A Clinical Trial In Georgia
Moving Clinical Trials away from Ukraine and Russia
Russia, Ukraine, and other CIS countries have been significant ...
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 ...
Artificial Intelligence in Pharmacovigilance
Automation & AI in Pharmacovigilance: Promises and Realistic Expectations
Recent years have seen increasing ...
