PHARMACEUTICAL ONLINE RECENT WEBINARS
Scaling Up Your E. Coli pDNA Process From Parameter Screening To Pilot Scale
Discover a systematic approach to scalable plasmid DNA production using E. coli OneShot Top10, which features DOE-driven optimization and key insights for efficient biomanufacturing success.
What Your Environmental Monitoring Isn't Telling You
Explore overlooked contamination sources, like residues, poor housekeeping, and training gaps, which offer practical strategies to strengthen your contamination control program.
The Pathway To Operational Readiness
Ready to ensure your facilities, systems, and teams are prepared for success from Day One? Discover a proven framework to accelerate operational readiness, mitigate risks, and achieve sustainable results.
Proven Strategies For GxP Compliance And Inspection Readiness
Struggling with data integrity challenges? Discover proven strategies for GxP compliance and inspection readiness in this essential webinar. Learn to build a robust framework and avoid common pitfalls.
Cleanroom Conceptual Design Paradigm: Converting Spaces For GMP Operations Part 2
Learn essential conceptual design principles for transforming alternative spaces into efficient, regulatory-aligned cleanroom environments for your critical processes.
Unlocking Efficiency In Large-Scale Microbial Manufacturing
Gain insights into how expert teams and the right tools help build resilience into manufacturing systems and tackle small, often-overlooked issues before they become costly problems.
Seals And Stability: Preventing Failures In Synthesis And Chromatography Columns
Unlock the key to long-term column performance and stability. Learn how crucial seal maintenance can prevent catastrophic failures and safeguard your therapeutic products.
Optimizing The Progression Of Biotherapeutic Candidates To FIH Studies
Learn actionable strategies that can lead to higher success rates and smarter resource investment, paving the way for a successful path to IND submissions and commercialization.
A New Look At Subcutaneous mAb Delivery Using Nanoformed Particles
A highly concentrated non-aqueous suspension of an IgG1 was developed using a patented platform. Review how the particle size of the monoclonal antibody (mAb) impacts the overall behavior of the drug product.
Peptones And Vaccines: A Synergistic Approach To Enhanced Production And Efficiency
Enhance your vaccine manufacturing with peptones. Explore their benefits, analyze data-driven productivity gains, and learn integration strategies in this informative, on-demand session.
Building A Purification Toolkit For An Expanding Variety Of mAb Therapeutics
Explore techniques for optimizing purification toolkits for various monoclonal antibody formats. This session covers resin and buffer selection for efficient downstream process development.
How To Optimize Labeling In A Pharmaceutical Environment
Accurate, readable pharmaceutical labels are crucial. Learn to navigate considerations like printing, application tolerances, and inspection to select the right machinery for your production environment.
Accelerate And Enhance Biomanufacturing Operator Training
Unlock the power of blended operator training and learn how combining digital tools with hands-on instruction reduces errors, boosts retention, and empowers your workforce for real-world production success.
Maximizing Media Strategies: Expert Insights On Boosting Performance
Optimize biopharma media strategies for consistent protein quality. Experts discuss formats, variability, and actionable analytics in this on-demand virtual roundtable.
Navigating Regulatory Shifts: EU GMP Annex 1 And USP 382
Strengthen risk mitigation strategies while ensuring regulatory alignment. Gain valuable insights into best practices and proactive approaches for building a robust and future-ready CCS.
Utilizing A Stepwise Approach For Nitrosamine Risk Mitigation
The following insights and case studies demonstrate how a tailored, stepwise testing approach can effectively detect, quantify, and control nitrosamine impurities while maintaining cost efficiency.
Digital Transformation In Contract Manufacturing: A Leadership Perspective
Discover how PCI Pharma Services embraced digital transformation and gain expert insight on overcoming challenges, driving innovation, and maintaining core values in a regulated industry.
PUPSIT Without The Pain: Practical Solutions For Implementation
Explore the critical role of pre-use post-sterilization integrity testing in quality risk management, as well as learn about integrity testing, wetting procedures, and innovative filtration systems for effective implementation.
Accelerating Technology Transfer Through Unified Recipe Management
See how a unified recipe authoring workflow can reduce technology transfer times in manufacturing, enhance validation efficiency, and streamline operations by integrating process control systems.
CLD To Upstream Optimization: Enhancing Biologics Quality, Productivity
Explore how advanced cell line development and upstream processing strategies optimize both productivity and therapeutic effectiveness, ensuring the development of high-quality biologics.
3D Screen Printing: Breakthrough Solutions For Patient-Centric Therapies
Explore 3D screen printing’s potential to revolutionize pharmaceutical manufacturing with scalable, customizable, multi-drug tablets and precise, patient-centric drug release profiles.
Inside The Development Of An AAV8 Production Platform
Explore innovative solutions for AAV8 production challenges, which include scalability and purity, as well as learn how a collaboration with CDMO Matica Biotechnology ensures efficient, high-yield gene therapy vector production.
Sustainable Manufacturing Through Efficient BioProduction Unit Operations
Delve into the critical environmental and economic aspects of bioprocessing. Explore the urgent need to manage the industry’s growing plastic waste issue and a three-pronged approach to address this challenge.
Navigating Global Regulatory Landscapes In An Evolving Biopharma Industry
Minimize regulatory risks and ensure compliance in the evolving biopharma sector. Watch this on-demand discussion for insights on change management, supplier collaboration, and future market trends.
Transforming Rare Disease Drug Development For A Faster Cure
This comprehensive exploration aims to shed light on the critical aspects of expediting curative therapies, with a focus on the strategic role that CDMOs can play in this transformative journey.
Curing The Cost Of Poor Quality: How Argon Medical Found The Remedy
Discover how poor quality can cost your organization up to 20% of its revenue and learn how Argon Medical's eQMS helped them reduce defects, waste, and complaints.
Optimize Your Process For Producing High-Concentration Drugs
Explore the challenges and solutions in high-concentration monoclonal antibody manufacturing, which includes practical strategies for maximizing product recovery and optimizing processes for efficient production.
Development Strategies For Platform Devices Navigating Regulatory Complexities
Explore regulatory strategies for platform drug-device products, including bridging formulations, leveraging existing data, and aligning with FDA expectations to accelerate market access and reduce risk.
Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing
Learn about an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.
Driving Innovation In Decentralized Manufacturing
Unlock the potential of localized manufacturing and see how cutting-edge technology is transforming access to essential medications, ensuring patients get what they need.