Explore UV-Vis, PDA, Fluorescence, RID, MS, and Conductivity detectors in HPLC. Learn strengths, limits, and applications in pharma R&D and QC. 🔗 Read the full article: hubs.li/Q03ZPjR40 #HPLC #Pharma #QualityControl #QC

Hello 2026! ✨ From the entire QbD Group team, we wish you a wonderful year filled with good health, fruitful collaborations, and plenty of joy along the way. Happy New Year! 💙 #NewYear #BestWishes #QbDGroup

AI providers and deployers must ensure AI literacy as of Feb 2025. Learn what it means, who’s responsible, and how to turn compliance into opportunity. 🔗 hubs.li/Q03WTHB_0 #AIAct #ArtificialIntelligence #LifeSciences

Did you know 'QbD' stands for 'Quality by Design'? So, it's no surprise that raising the bar on quality is in our DNA. ✨ Need an audit? QbD's certified experts execute global GxP, MDR & IVDR audits, wherever you operate. 🌍 hubs.li/Q03SQ5KH0 #WorldQualityDay #Audit

We receive questions about Computer System Validation (CSV) every single day, from clients, partners, and industry experts alike. We’ve put together a practical FAQ guide with 45+ questions from the field. 🔗 Download: hubs.li/Q03Qd7_30 #CSV #Digitalization #FAQ

Improve audit planning, execution, and follow-up in life sciences with a structured, risk-based approach—plus when and why to consider external QA support. 👉 Read the full post here hubs.li/Q03Gl2220 #LifeSciences #AuditPlanning #QualityAssurance

Veterinary pharmacovigilance audits are key to global health. Discover how QbD Group helps you comply with VGVP and ensure veterinary drug safety. 💊🐕 👉 hubs.li/Q03Dytg70 #VeterinaryPharmacovigilance #Pharma #AnimalHealth

Healthcare professionals and patients both play a vital role in reporting adverse events — a key pillar of effective #pharmacovigilance. Learn more in our blog 👇 hubs.li/Q03xCn5l0

earn how Good Distribution Practices (#GDP) and Quality Risk Management (#QRM) ensure the integrity, safety, & compliance of pharma products during distribution. 🔗 hubs.li/Q03xCg_m0

Achieve IVDR compliance for large-panel Next-Generation Sequencing (NGS). Validate genetic variants and meet performance requirements with the right strategy. hubs.li/Q03xCmWB0 #NGS #IVDR #InVitroDiagnostics #EU

Learn how to optimize pharmacovigilance systems and outsource strategically to turn compliance into business growth. 🔗 Read the full article: hubs.li/Q03xCnKP0 #Pharmacovigilance #Pharma

"Digital health"—everyone's talking about it, but what does it really mean? 🤔 With so many definitions out there, it can feel like a jungle! Ready to make sense of digital health? Download the whitepaper now 👇 hubs.li/Q03xCnT40

Learn how to build a contamination control strategy (CCS) under Annex 1. Key elements, scope, risk control, and inspection-readiness tips included. hubs.li/Q03xCn7p0 #Annex1 #Pharma #CCS #ContaminationControlStrategy

Learn how GMP labs can strategically balance quality, cost, and time using smart technologies, risk-based approaches, and lean workflows. 👉 Read more: hubs.li/Q03xCnKK0 #GMP #Lab #QC #QualityControl

Discover how the EU’s Critical Medicines Act and ESMP aim to prevent drug shortages and build a resilient medicine supply for Europe’s future. Read more 👉 hubs.li/Q03sBbgG0 #Pharma #EU #Medicine #CriticalMedicinesAct #ESMP

Learn the essentials of Pharmacovigilance Agreements (PVA) and Safety Data Exchange Agreements (SDEA) to ensure regulatory compliance and effective collaboration. Read more 🔗 hubs.li/Q03s8PDJ0 #DrugSafety #Pharmacovigilance #PVA #SDEA

We’re very proud to share that QbD Group has once again been recognized as one of Belgium’s #BestManaged Companies, earning the Gold Label for the second consecutive year. ✨ 🔗 Read the full press release: hubs.li/Q03nWhv_0

Big news at QbD Group! 📢 This week we were very happy to welcome Angeles Escarti-Nebot as the new Division Head of our Regulatory Affairs division. Read the full press release: 🔗 hubs.li/Q03lnGml0 #RegulatoryAffairs #LifeSciences

Are you in line with the current medical device QMS requirements? We’ve developed an ISO 13485:2016 checklist to help you stay compliant and save time. 📥 Download it here: hubs.li/Q03jg26z0 #ISO134852016 #QMS #MedicalDevices #QualityAssurance

Learn the key requirements of GMP Annex 21 for importing medicines into the EU, including MIA compliance, QP certification, and supply chain responsibilities. 👉 hubs.li/Q03hNbtv0 #Pharma #GMP #Annex21