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Discovery of Circulating Protein Biomarkers by Analysis of the Tissue Secretome
Best Practices for Conducting Extractable and Leachable Studies
Predictive Biomarker Discovery for Oncology Small-Molecules and Biologics
How the Medical Device Industry Can Prepare for the EU Regulatory Changes Ahead
Best Practices for Tracking Tissue in the Healthcare Supply Chain
Optimizing Trial Outcomes through Computer Assisted Design
Impacting Clinical and Preclinical Decisions: Computational Analysis of Complex Genomics Data Sets
Development of an Innovative Microtablet Dosage Form
Monitoring Protein Synthesis One Codon at a Time Through Ribosome Profiling
Adhering to Good Clinical Practice: An Overview of Clinical Trials
DMPK for Targeted Tissue Delivery: Solutions for the Most Challenging Part of Outsourcing
Post-Marketing Observation Studies (PMOS) and Phase IV Studies
S.E. Asia Drug/Device Update: Market Potential and Regulatory Environment
Accelerating Drug Development by Harnessing Technology
Removing the Risk in Risk-Based Monitoring – A Practical and Proven Approach to Implementing Central Statistical Monitoring
Ensuring Distribution Readiness Before FPI: A Simple Guide to De-Risking
Endpoint Based Protocol Development: A Central Laboratory Perspective + Microbiology Case Study
Leveraging an Academic-Industry Partnership for Commercial Success
Adherence in Asthma: Comparing Clinical Trials to the "Real-World"
Clinical Process Innovation: Driving Predictability in Clinical Development through Innovation
Clinical Development, Contracts and Outsourcing in MENA & APAC
Translational Animal Models of Pain
Optimize Your Product Launch in a Multi-Stakeholder Environment
Practical Uses for Flow Cytometry in Toxicology Studies Within a GLP Environment
Managing Cultural Variability in PRO Measurement in Global Clinical ResearchPart 1: Cross-cultural Qualitative Research for Simultaneous Scale Development
Risk-based Thinking: The Success of Risk-based Monitoring Begins with Risk-based Thinking