Webinar channel: Pharma
Welcome to the Business Review Webinars Pharmaceutical channel, dedicated to bringing you live fully interactive webinars on the latest topics in the Pharma industry.
Our Pharmaceutical channel keeps you up to date in areas such as drug discovery, drug development, drug formulation, clinical development and clinical trials. The 60 minute webinar sessions are presented by leading businesses and organisations such as Thomson Reuters, Covance and World Courier and are aimed at giving business insights, educational value and access to new techniques and products without the need to travel.
All of our Live Upcoming and On Demand webinars are free to attend and can be viewed on a PC, Mac, or via your Smart Phone app. Simply choose a webinar session below and register.
We also host webinars in Energy, Food & Beverage, Supply Chain and Healthcare.
Upcoming Webinars
On Demand Webinars
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Leveraging mRNA to Revolutionize Antibody Manufacturing
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You're Hired! Selecting the Right Pre-IND Compound
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Navigating the Complexities of Early Ion Channel Drug Discovery
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How Loftware Smartflow Transformed Orion Corporation’s Artwork Management
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Multi-cell models for neuroinflammation and myelination
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ISO 14698 Remote Microbial Air Sampler Flexible Solution
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TiO2-Free Capsules: Navigating Regulatory and Technical Challenges
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Optimizing Combination Device Design for Arthritic Hands
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Optimizing Combination Device Design for Arthritic Hands
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Navigating Nasal Spray Drug Product Development Process through Approval
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Analytical Development in Cell and Gene Therapy: Setting up for Success
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Business Continuity Planning: Engineered Energy and HVAC Solutions for the Pharmaceutical Industry
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Accelerating Batch Release in QC Labs
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Early de-risking of pre-clinical drug candidates
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Enhancing Decentralised Clinical Trials: The Power of Direct to Patient Distribution
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Vision for the Future: Automation and Gen Z – Challenges and Opportunities for Leaders
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Advancing Antibody Drug Conjugate (ADC) Discovery Against Cancer
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Mastering CMC Strategies in Cell and Gene Therapy
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Optimizing Soft Gelatin Capsules
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The Art of CCIT: Deterministic Method Selection
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The Art of CCIT: Deterministic Method Selection
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Transitioning pMDI’s products with Low Global Warming Propellants
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De-risking and accelerating small molecule development, from whiteboard to first-in-human
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De-Risking the Development of Sensitive Injectables
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De-Risking the Development of Sensitive Injectables
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AI in R&D: Real Impact, Real Results
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Breaking Barriers: Optimizing Inhalation Capsules for Enhanced Drug Delivery
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Revolutionizing Clinical Trial Service Provider Qualification
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Transforming Biopharma Quality through an AI-driven Approach
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Optimizing Preclinical Studies for Intranasal and Pulmonary Programs
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Optimizing Preclinical Studies for Intranasal and Pulmonary Programs
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AI and Automation in Packaging Artwork & Labeling
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In Silico Modelling for Orally Inhaled Drug Development
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In Silico Modelling for Orally Inhaled Drug Development
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API feasibility studies for TTS and OTF
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A Unified Data Platform Delivers Integrated PAT and CPV
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Raising the Bar for Injectable Drugs: EU GMP Annex 1 and Its Impact
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Raising the Bar for Injectable Drugs: EU GMP Annex 1 and Its Impact
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Environmental Monitoring Compliance Learning from FDA Warning Letters
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Breaking Free from Chromatography: Transformative AAV Purification
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Designing Extractable/Leachable Studies for Drugs and Biologics
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Advancing Inhaled & Nasal Drug Clinical Studies
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Advancing Inhaled & Nasal Drug Clinical Studies
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Process Development of ADCs and Bioconjugates
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From Lead Candidate to GMP Manufacture - Navigating the Drug Substance Development Journey
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Voice-to-ELN: How LabTwin & Revvity Signals Notebook connect to boost productivity in the lab
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Biopharmaceuticals, Cell and Gene Therapy. Single-Use Technology and Extractable/Leachables: Is your...
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AI-Driven Drug Design: Exploring Novel Cancer Therapeutics with Generative Design
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Integrated CDMO solutions for parenteral drugs
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A Comparative Study of P134a and P152a Spray Characteristics and Human-Realistic Mouth, Trachea, and...
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How to Streamline Leaflet Creation with Automation
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Evolution of Immunogenicity Assessment
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Single-use: How To Reduce Your Dependency On Filtration
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How is innovation disrupting small molecule hit identification?
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mg to kg: Discovering Optimal Solid Forms of Drug Substances
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How to Make Successful Hit Finding Choices
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Portable Particle Counting and meeting GMP Annex 1
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OBDS - On Body Delivery Systems
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How to Accelerate Drug Product Optimization Using Translational Pharmaceutics®
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Ensuring Container Integrity at Various Temperatures
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Ensuring Container Integrity at Various Temperatures
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Platform Analytical Strategies Enable an Expedited Path to IND
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Unlocking the benefits: Managed Access Programme delivery utilising a Just in Time Manufacturing app...
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Leveraging AI in Accounts Payable
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Unlocking the Power of Capsules
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A Risk-Based Approach to Vendor Qualification and Management
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DMPK in Small Molecule Drug Discovery–The What, Why, & When
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E&L Considerations for Injectables & FluroTec Closures
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Capsule-based inhalers:solutions for now & future challenges
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Mitigating the Risk of Pitfalls in Nasal Drug Development
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Approaches to Extractables and Leachables in Parenteral Drugs
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Approaches to Extractables and Leachables in Parenteral Drugs
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Creating Drug Discovery Strategies for Therapeutic Success
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Annex 1 Questions and Answers
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Mitigating the Risk of Pitfalls in Nasal Drug Development
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Empowering DSM scientists with voice-powered digital lab assistants to improve R&D efficie...
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SMARTag® Technology, from Bertozzi Lab to Best-in-Class ADCs
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Site Collaboration in a Digital Ecosystem
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Site Collaboration in a Digital Ecosystem
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TEST FOR VEEVA
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Strategies for Achieving Regulatory Milestones Faster: An Ensysce Biosciences & Quotient Science...
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The Virtual Twin of Processes and Equipment to Support Modular Biomanufacturing
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Mastering the translation of clinical trial labels
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The rare disease patient experience
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Partnering with CDMOs for a sustainable future
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West Pharma - State-of-the-art 4040 Elastometer-A deep dive
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PIXEL PROOF+Saas Web based text and image proofing solutions
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Understanding the role of Non-Interventional Studies (NIS) in the generation of Real World Evidence:...
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Characterizing and Controlling Foreign Particle Matters (FPM)
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Characterizing and Controlling Foreign Particle Matters (FPM)
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Vaccine clinical trials with RNA-Seq endpoints to measure gene expression - Lessons Learned
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Top Performers Do It Differently: Learn How Astrazeneca Achieved 95% Automation By Standardizing Pro...
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Are Outcome Measures Failing Our Patient Populations
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Streamlining the Delivery of 14C Human ADME Data: An ADME Q&A Roundtable
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Streamlining the Delivery of 14C Human ADME Data: An ADME Q&A Roundtable
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The Tablet Characterization with Regulatory Compliance Methods – USP<1062>
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Floor Surface Contamination in Controlled Environments
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Micro Array Patches – case study for Interferon-ß and Hepatitis-B-Vaccination
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Leveraging Stable Pool Material to Expedite the Path to IND
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From pMDI Device to Therapeutic Effect
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