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.
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Biomapas Insights: Clinical Site Selection for Early Phase Oncology Studies
Expert perspectives on where to begin, how to choose the right clinical sites, and what to consider when selecting an eCRF/EDC system for early-phase oncology studies.
Case Study: Specialised Rescue Studies in Georgia
Discover how we successfully supported late‑phase clinical trials in Georgia by overcoming operational ...
Comprehensive Guide to Medical Information and Pharmacovigilance Integration
Discover how integrated Medical Information and Pharmacovigilance workflows enhance compliance, improve safety, and streamline regulatory processes.
Biomapas Insights: From Hope to Global Impact – How Elpida Accelerated Gene Therapy for Rare Diseases
In this Biomapas Insights episode, Martijn van de Leur, Chief Commercial Officer, speaks with Terry Pirovolakis, ...
Biomapas Insights: Selecting the Right CRO at the right time – What Biotechs Need to Know
Expert insights on timing, selection criteria, and early-phase clinical trial strategy for choosing the right CRO in biotech development.
Running Pan‑European Multi‑Regional Trials with Flexible FSP Models
Discover how flexible FSP models help sponsors run multi-country clinical trials across Europe with greater control, speed, and regional alignment.
Choosing the Right QPPV Partner for EU and Global Compliance
Explore the essential functions of a QPPV and discover how to choose the right partner for pharmacovigilance.
How to achieve Multi-Region Pharmacovigilance Compliance: Critical Lessons from CIS and MENA
Explore the challenges of multi-region pharmacovigilance and learn strategies for compliance in CIS and MENA markets.
Enhancing Patient Recruitment in Niche Markets Through Clinical Trial Outsourcing
Explore clinical trial outsourcing and its role in overcoming recruitment challenges in clinical research for small biotech companies.
The use of AI/Automation in Pharmacovigilance: Ensuring Safety through Robust Processes
Discover how AI and automation are transforming pharmacovigilance, including Veeva’s signal management solutions, the role of NLP and machine learning in safety workflows, and future trends in AI.
Signal Detection: An Integrated Approach to Pharmacovigilance & Regulatory Compliance
Discover how efficient signal detection manages safety risks, ensuring compliance with global regulations.
Global Literature Review: Ensuring Safety through Robust Processes
Learn how our end-to-end GLR process enhances patient safety and supports regulatory compliance worldwide.
Site Startup Services in Clinical Trials: Leveraging Local Expertise
Learn how integrating site startup services within a flexible FSP model accelerates activation in CIS and CEE, reduces contract cycles, and improves predictability from first submission to first patient in.
Pharmacovigilance outsourcing for boosting compliance and safety for biotech companies
Explore why pharmacovigilance outsourcing is essential for biotech companies in 2025 to ensure compliance and patient safety.
Local Affiliate Services That Deliver the Best Results
Find out how local affiliate services can reduce compliance risks and support effective regulatory strategies in the pharma industry.
The Perfect Partnership: How Mid-Sized CROs and Site Networks Deliver Clinical Trial Success
In this webinar, learn how the right size of CRO and the right type of site network partnership can deliver clinical trial success.
Breaking the Silos Across Medical Information & Pharmacovigilance – Leveraging Technology for Operational Efficiency
This whitepaper shows how a PV/MI Single Source of Truth boosts data management, compliance, and efficiency for complex therapies.
Harmonizing Product Information Across Baltic Markets
Navigating multilingual product information across several markets can be complex – but it doesn’t have to be.
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Dossier Transformation for Market Expansion
Struggling with outdated dossiers and complex regulatory requirements? We partnered with a large pharma company to ...
Whitepaper: Computerised System Validation & Pharmacovigilance
This whitepaper explores how optimised computer system validation (CSV) strategies strengthen risk management, ensure data integrity in pharmacovigilance systems, and support compliance through a real-world cloud-based safety database case study.
