Explore UV-Vis, PDA, Fluorescence, RID, MS, and Conductivity detectors in HPLC. Learn strengths, limits, and applications in pharma R&D and QC.
π Read the full article: https://t.co/kr7LakR1ZR
#HPLC#Pharma#QualityControl#QC
Hello 2026! β¨
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! π
#NewYear#BestWishes#QbDGroup
AI providers and deployers must ensure AI literacy as of Feb 2025. Learn what it means, whoβs responsible, and how to turn compliance into opportunity.
π https://t.co/MRAhqHwBWZ
#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. β¨
Need an audit? QbD's certified experts execute global GxP, MDR & IVDR audits, wherever you operate. π
https://t.co/VWbL6uZJfX
#WorldQualityDay#Audit
We receive questions about Computer System Validation (CSV) every single day, from clients, partners, and industry experts alike. Weβve put together a practical FAQ guide with 45+ questions from the field.
π Download: https://t.co/nfWK8MyDQk
#CSV#Digitalization#FAQ
Improve audit planning, execution, and follow-up in life sciences with a structured, risk-based approachβplus when and why to consider external QA support.
π Read the full post here https://t.co/FODoYebKTA
#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. ππ
π https://t.co/GYmRwqtr9L
#VeterinaryPharmacovigilance#Pharma#AnimalHealth
Healthcare professionals and patients both play a vital role in reporting adverse events β a key pillar of effective #pharmacovigilance.
Learn more in our blog π
https://t.co/DITxZlo0pg
earn how Good Distribution Practices (#GDP) and Quality Risk Management (#QRM) ensure the integrity, safety, & compliance of pharma products during distribution.
π https://t.co/DAAQw0DB3m
Achieve IVDR compliance for large-panel Next-Generation Sequencing (NGS). Validate genetic variants and meet performance requirements with the right strategy.
https://t.co/OWhiSWYcHx
#NGS#IVDR#InVitroDiagnostics#EU
Learn how to optimize pharmacovigilance systems and outsource strategically to turn compliance into business growth.
π Read the full article: https://t.co/3JfMZHGNsa
#Pharmacovigilance#Pharma
"Digital health"βeveryone's talking about it, but what does it really mean? π€ With so many definitions out there, it can feel like a jungle!
Ready to make sense of digital health?
Download the whitepaper now π
https://t.co/S5evG60moy
Learn how to build a contamination control strategy (CCS) under Annex 1. Key elements, scope, risk control, and inspection-readiness tips included.
https://t.co/otLdWv2ipG
#Annex1#Pharma#CCS#ContaminationControlStrategy
Learn how GMP labs can strategically balance quality, cost, and time using smart technologies, risk-based approaches, and lean workflows.
π Read more: https://t.co/5OmLtIHWlR
#GMP#Lab#QC#QualityControl
Discover how the EUβs Critical Medicines Act and ESMP aim to prevent drug shortages and build a resilient medicine supply for Europeβs future.
Read more π https://t.co/Uk3DhzJBgu
#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 π https://t.co/ZXvvHMLBN9
#DrugSafety#Pharmacovigilance#PVA#SDEA
Weβre very proud to share that QbD Group has once again been recognized as one of Belgiumβs #BestManaged Companies, earning the Gold Label for the second consecutive year. β¨
π Read the full press release: https://t.co/Koau20voI2
Big news at QbD Group! π’
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: π https://t.co/uksajGtMXm
#RegulatoryAffairs#LifeSciences
Are you in line with the current medical device QMS requirements?
Weβve developed an ISO 13485:2016 checklist to help you stay compliant and save time.
π₯ Download it here: https://t.co/5CuU3m2UTY
#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.
π https://t.co/LdJlasmTbr
#Pharma#GMP#Annex21