Webinars Regulatory Expectations: Bayesian Guidance from the FDA, CDE, and EMA July 21st, 2026 1 minute read Bayesian methods are increasingly being considered to support dose optimization, extrapolation, and adaptive designs ...
Webinars AI for Clinical Research Series – Prediction June 26th, 2026 1 minute read Augmenting Clinical Trials with Synthetic or Simulated Patients, Projecting Long-Term Benefit-Risk, and Developing Re...
Webinars A Systematic Review into the Use of Bayesian Methods in Clinical Trials June 25th, 2026 2 minute read Bayesian methods continue to gain momentum as an alternative approach to traditional clinical trial design, yet many ...
Webinars AI for Automation and Digital Data Flow June 24th, 2026 1 minute read Automate Programming and QC Processes, Accelerating Operations and Evidence Generation This session will explore AI’s...
Webinars Bridging the Efficacy-Effectiveness Gap in Rare Diseases June 18th, 2026 1 minute read Drug development in rare diseases requires the most efficient use of limited data, across both clinical trials and re...
Webinars Identifying the Best Populations to Target, De-Risking Discovery and Early-Stage Development June 3rd, 2026 1 minute read About This Webinar In this session, we explore real-world use cases where AI and LLMs (Large Language Models) have be...
Webinars Causal Inference Through a Regulatory Lens May 15th, 2026 1 minute read About This Webinar As expectations for robust, real-world evidence continue to grow, understanding how regulators eva...
Webinars From Data to Decisions: TMLE, Doubly Robust Methods, and Federated Learning April 13th, 2026 1 minute read This webinar will cover methods that are crucial to making informed decisions. Specifically, personalized care throug...
Webinars Causal Inference in Real World Evidence: What is it? Why now? January 22nd, 2026 1 minute read Causal inference is increasingly used to generate real-world evidence (RWE), by regulatory&n...
Webinars Regulatory-Grade Use of External Data: Bayesian Borrowing, Hybrid Trials and External Controls November 20th, 2025 1 minute read Use of external data to augment clinical trials has been increasingly evaluated and is transforming drug development ...
Webinars SDTM Workflow Transformation: Faster, Easier and More Reliable November 14th, 2025 1 minute read The demand for rapid, cost-effective, and standards-compliant SDTM delivery continues to increase across the biotech ...
Webinars Early Phase Clinical Trials: Key Considerations for Drug Development Pipelines October 30th, 2025 1 minute read The early stages of clinical development are critical, decisions made here can determine the efficiency, cost, and ul...
Webinars Use of Real-World Data for in-silico Trials and Innovative Designs: Recent Successes and Current Perspectives October 2nd, 2025 1 minute read Real-world data (RWD) are transforming clinical research. By supplementing randomized controlled trials (RCTs), RWD c...
Webinars DMC Best Practices: What Biotechs and Sponsors Should Know August 5th, 2025 1 minute read Data Monitoring Committees (DMC) are a critical part of the clinical trial process, independently assessing the safet...
Webinars Harnessing Bayesian Methods: Tackling Challenges in Rare Disease and Small Population Trials May 27th, 2025 1 minute read Sponsors working in rare diseases/running small population studies often have difficulties in demonstrating efficacy ...
Webinars Leveraging Real-World Evidence: Data Sources, Challenges and Applications in Modern Clinical Trials April 29th, 2025 1 minute read Real World Evidence (RWE) plays a critical role across multiple pharma processes, including drug development, regulat...
Webinars Novel Research in Early Phase Trials: Enhancing Efficiency of Combination Strategies February 28th, 2025 1 minute read Early phase trials play a crucial role in drug development, determining the dose to test in later phases. With the ri...
Webinars Strengthening Causal Inference with Sensitivity Analyses: Using the Bayesian Parametric G-Formula February 19th, 2025 2 minute read Understanding causal relationships in real-world data is challenging, particularly in observational studies, where co...
Webinars Mastering Clinical Trial Outsourcing: FSP Solutions from Industry Experts November 25th, 2024 2 minute read In Partnership With PCMG Phastar and PCMG partnered to start 2025 with an insightful fireside chat, sharing their ind...
Webinars Navigating the Real- World: How to Better Utilize Real-World Evidence October 29th, 2024 2 minute read Real World Evidence (RWE) is playing an important role in the drug development process by providing valuable insights...
Webinars EU HTA: Challenges and Opportunities September 19th, 2024 1 minute read With the upcoming introduction of the new EU HTA guidance in January 2025, sponsors in the pharmaceutical, Biotech an...
Webinars Navigating Project Optimus: Implications for Oncology Drug Development June 27th, 2024 2 minute read With the launch of Project Optimus, the FDA is reforming the dose optimization and dose selection paradigm in oncolog...
Webinars Implementing a Gold Standard FSP Strategic Partnership to Fuel Efficient Drug Development March 7th, 2024 1 minute read Complete the form below to watch the webinar Featuring: Moderated by Natalie Fforde, Senior Vice President, Global St...
Webinars Implementing Additional Medidata Solutions February 27th, 2024 1 minute read Slides created by: Carly Baker, Director, Clinical Data Operations, and Kat Fogden, Principal Data Operations Program...
Webinars The New Drug/Biologics License Applications Review Process. What’s all the Fuss? January 29th, 2024 1 minute read Presented by: LaRee Tracy, PhD, and Joshua Baker, PhD Complete the form below to watch the webinar
Webinars Statistical Insights for Biotech Professionals December 12th, 2023 1 minute read Complete the form below to watch the webinar
Webinars Understanding the Pitfalls of P-values and Hypothesis Tests December 7th, 2023 1 minute read Complete the form below to watch the webinar
Webinars Study Design Considerations for Biotechs November 30th, 2023 1 minute read Complete the form below to watch the webinar
Webinars Use of Expert Prior Elicitation for Clinical Research November 16th, 2023 2 minute read About this webinar The application of expert prior elicitation in clinical research serves as an important methodolog...
Webinars A Four-step Strategy for Handling Missing Outcome Data in Randomised Trials Affected by a Pandemic December 17th, 2021 1 minute read Presented by: Professor James Carpenter | MRC Clinical Trials Unit, LSHTM Complete the form below to watch the webinar
Webinars So, you want to meet the FDA? Preparing for Regulatory Meetings & How Statisticians can Influence these Interactions November 19th, 2020 1 minute read Presented by: LaRee Tracy, PhD, and Joshua Baker, PhD Complete the form below to watch the webinar
Webinars The Role of Industry and FDA Statisticians November 2nd, 2020 1 minute read Presented by: LaRee Tracy, PhD, and Joshua Baker, PhD Complete the form below to watch the webinar
Webinars Clearing the Fog: An introduction to LOINC codes September 18th, 2020 1 minute read Presented by: Jordan Bristow | Phastar Complete the form below to watch the webinar
Webinars Blinded by the X-Rays? An Introduction to the Design of Radiotherapy Trials September 16th, 2020 1 minute read Presented by: Lucy McParland | Phastar Complete the form below to watch the webinar
Webinars Data Management’s Role in Multi Stream Data Capture August 30th, 2020 1 minute read Presented by: Kirsty Millar | Phastar Complete the form below to watch the webinar
