Webinars
Register for our upcoming webinars or browse our on-demand webinar library to hear from experts who are breaking ground in their fields of scientific research.
Pharma and biopharma manufacturing, Gene therapy manufacturing
Advancing AAV Purification: New Approaches to Improve Performance and Reduce Cost
AAV purification remains one of the largest contributors to manufacturing costs in gene therapy. Join this webinar to explore emerging purification approaches, validation strategies, and practical considerations for improving process efficiency while supporting scalable, affordable therapies.
Peter Menstell
Merck
Senior Scientist
Dr. Carl Christel
Revvity
Sr. BD Manager, CGT - Europe - Revvity
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 20 August 20263:00 PM, CEST
Pharma and biopharma manufacturing, Downstream Processing
Process Intensification for Bispecific Antibodies: Flocculated Harvest & Flow-Through Polishing
In this informative session, you'll gain practical insight of how to handle high-cell-density harvest, and how to achieve purity goal utilizing flow-through polishing. Join us to discover how moving towards process intensification can drive value of the downstream process of bispecific antibody.
Karen Chan
Merck
Head of Downstream MSAT, SEA & Taiwan
Wei-Che Lin
Mycenax
Principal Scientist
Anna Lee
Merck
Customer Application, Downstream
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 25 August 20262:00 PM, SGT
Pharma and biopharma manufacturing, Pharma and biopharma manufacturing
Bringing Breakthrough Science to Life: Process Development Services for Emerging Biotech
Process Development Services help biotech startups overcome bottlenecks, optimize tech choices, and advance programs with real case studies and reflections.
Teresa Vargas
Merck
Process Development Scientist - Emerging Biotech
Jaime De Souza
Merck
Senior Process Development Scientist - Emerging Biotech
Demetri Maxim
Nephrogen
Co-Founder and CEO at Nephrogen
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 10 September 20265:00 PM, CEST
Small Molecules Analysis and Quality Control, Pharma and biopharma manufacturing
Pediatric Formulations: Meeting Big Challenges for Little Patients
Join our Webinar on Pediatric Formulations to tackle practical challenges in oral solid and liquid pediatric formulations, navigate the regulatory landscape, explore functional excipients, and our portfolio offerings.
Manisha Chaudhari
Merck
Head of Customer Applications-Excipient, APeC
Suruchi Vishwasrao, Ph.D.
Merck
Senior Scientist
Dr. Pratik Kakade
Merck
Senior Customer Application Expert - Excipient
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 15 September 20262:00 PM, SGT
Đang hiển thị 1 - 4 trong số 4 kết quả
- Trang 1
Pharma and biopharma manufacturing, Downstream Processing
Sterile Filtration in the Annex 1 Era: Interpreting PDA TR 26 (Revised 2025)
In the Annex 1 era, sterile filtration is no longer about validating a filter—it’s about demonstrating a robust, risk-based system that ensures sterility at every step.
Partha Banerjee
Merck
Technical Application Expert, Downstream India
Aria Kang
Merck
Regional Strategy Execution Manager - Downstream Process
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 4 August 2026
Pharma and biopharma manufacturing, Sterile Filtration Strategies
Optimizing Bioburden Control for Enhanced Biomanufacturing Efficiency
Elizabeth Sally Thomas
Merck
Senior Strategic Product Manager, Aseptic Filtration- Downstream Processing & Validation Services
Faith Gilmore
Merck
Senior MSAT Engineer
- Thời gian:
- 1 hr
- Dữ liệu:
- 30 July 2026
Pharma and biopharma manufacturing, Gene therapy manufacturing
Detergent-Mediated Viral Inactivation for Multiple Modalities
Janice Tan, Ph.D.
Merck
Head of Upstream, Process Materials and Process Consultancy Asia Pacific excluding China
Kakolie Banerjee, PhD
Merck
R&D Manager (Virology), Scientific and Validation Services
Rain Lee
Merck
Customer Application Consultant
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 28 July 2026
Monoclonal antibody manufacturing, Gene therapy manufacturing
Trace Element Prediction - Data-Driven Understanding and Control of Impurities in Cell Culture Media
Discover how a data-driven TE prediction identifies high-risk materials and enables smarter formulation design for consistent cell culture media.
Kevin Kent
Merck
Senior Data Scientist
Corinna Merkel
Merck
Senior Scientist in Cell Culture Media Production
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 23 July 2026
Cell culture and analysis, Monoclonal antibody manufacturing
Beyond One-Size-Fits-All: Custom Media Optimization with Metabolic Flux Precision
Jeremy Riesberg
Merck
Principal Scientist, Media Development Services
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 16 July 2026
Pharma and biopharma manufacturing, Final Fill Strategies
Leachables & Peptide Stability: Science-Driven Risk Mitigation in Single-Use Drug Product Processing
Sarah Parsons
Merck
Senior Modality Leader
Ram Sheth
Merck
Senior Strategic Product Manager, Fill & Finish
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 9 July 2026
Pharma and biopharma manufacturing, Classical pharma manufacturing
Navigating Risk and Change - Day 3
This seminar delivers four distinct sessions on critical regulatory updates. Explore the intricacies of EU GMP Annex 1 air monitoring, MAT implementation, and RMM landscapes. It also covers Animal By-Product (ABP) regulations to ensure robust compliance and seamless market access.
Kenny Tay
Merck
Head of Commercial Applications, APAC
Dr. Rohit Bisht
PETA India
Senior Scientist- Regulatory Testing (Pharm & Med Devices), PETA India
Sha Zhu, Ph.D
Merck
Senior Regulatory Marketing Expert, BioMonitoring
Dr. Tobias Hertzig
Merck
Regulatory Affairs Expert
Parag Vachhani
Merck
Senior Expert in Regional Commercial Applications, APAC
- Thời gian:
- 4 hrs
- Ngôn ngữ:
- English
- Dữ liệu:
- 9 July 2026
Pharma and biopharma manufacturing, Classical pharma manufacturing
Navigating Risk and Change - Day 2
Explore regulatory strategies for ADCs and their components, align raw material management with ICH guidelines, navigate ATMP comparability requirements, and master GMP/GDP for excipients—delivering practical, risk-based guidance and actionable implementation tips.
Mandy Balleine
Merck
Senior Regulatory Affairs Expert (CDMO)
Janmeet Anant, Ph.D
Merck
Senior Regulatory Consultant
Houda Beltaief
Merck
Head of Biopharma Regulatory Experts
Mike Polito
Merck
Regulatory Expert, Pharma Materials
June Hwang
Merck
Senior Modality Leader for Advanced Antibodies
Jeong-Hoon Lee
Merck
Regulatory Management Specialist
Rain Lee
Merck
Customer Application Consultant
Dr. Saroj Varavadekar
Merck
Head of Regulatory Management, India
- Thời gian:
- 4 hrs
- Ngôn ngữ:
- English
- Dữ liệu:
- 8 July 2026
Pharma and biopharma manufacturing, Classical pharma manufacturing
Navigating Risk and Change - Day 1
Gain expert insights into the evolving regulatory landscape of excipient quality and SUS. This seminar addresses China’s NMPA updates, nitrosamine/DEG regulation compliance, and SUS standards. Learn to navigate complex requirements to ensure robust regulatory alignment.
Cloris Tian
Merck
Senior Regulatory Expert
Dr. Ulrich Reichert, M.D.R.A.
Merck
Head of CDMO and Bioprocess Materials
Yuwei Heinzel
Merck
Head of Pharma Registration
Simone Biel, Ph.D.
Merck
Senior Regulatory Expert
Manisha Chaudhari
Merck
Head of Customer Applications-Excipient, APeC
Kyung-Min Shin
Merck
Customer Application Consultant
Bennett Tan
Merck
Regional Strategy Execution Manager
- Thời gian:
- 4 hrs 3 mins
- Ngôn ngữ:
- English
- Dữ liệu:
- 7 July 2026
Gene Therapy Contract Development and Manufacturing, Gene Therapy Formulation and Final Fill
AAV Challenges and Solutions
Learn how to maximize AAV production, increase output, lower COGS, shorten time to clinic, and expand gene therapy initiatives.
Janice Tan, Ph.D.
Merck
Head of Upstream, Process Materials and Process Consultancy Asia Pacific excluding China
Subhasis Banerjee, Ph.D.
Merck
Principal Process Consultant
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 30 June 2026
Food and beverage testing and manufacturing, Microbiological analysis
Test Smarter, Stay Compliant: Validated Pathogen Detection Methods Built for Your Lab's Workflow
In this webinar, our food safety experts will guide you through the science and strategy behind selecting the optimal detection technology for your workflow.
Sally Powell Price, PGDip, MSc
Merck
Regulatory & Public Health Expert, F&B Safety Testing
Lyssa Sakaley MS, MBA
Merck
Senior Global Product Manager
Adam Didier, Ph.D.
Merck
Technical Lead, Food & Beverage
Khyati Shah, Ph.D.
Merck
Global Product Manager
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 30 June 2026
Pharma and biopharma manufacturing, Antibody drug conjugate manufacturing
Enhancing Virus Filtration Flux by Addressing Adsorptive Fouling
Discover why complex mAbs exhibit severe virus filtration flux reduction and how new membrane technology delivers over threefold flux increases.
Benjamin Cacace
Merck
Principal Engineer, Downstream Applications R&D
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 25 June 2026
Microbiological testing, Microbiological analysis
From Manual to Automated QC: Key Considerations, Challenges and Solutions
In this webinar, our experts will outline what to consider when evaluating and implementing automated solutions.
Anne Weeks
Merck
Automation & Robotics Specialist
Johannes Oberdörfer
Rapid Micro Biosystems
Senior Manager Field Applications
Tim Cser
Merck
Senior Technology Specialist, Commercial Applications
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 23 June 2026
Pharma and biopharma manufacturing, Antibody drug conjugate manufacturing
Material Considerations and Greener Alternatives: Navigating Regulatory Changes in Bioprocessing
In this insider session, we address material considerations such as for PFAs and highlight how the principles of sustainability can accelerate development of greener alternatives.
Alexander Mitropoulos
Merck
Director, Strategic Programs
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 18 June 2026
Analytical chemistry, Small molecule HPLC
Innovations in Sustainability: Your Path to Greener HPLC and LCMS
This webinar will explore multiple ways to achieve enhanced sustainability in HPLC and LCMS workflows, demonstrating that environmental responsibility and analytical excellence can coexist seamlessly.
Arne Egberts
Merck
Technology Manager
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 17 June 2026
Pharma and biopharma manufacturing, Solid Formulation Strategies
Pharmaceutical Co-crystals: Evolving Global Regulatory Perspectives.
Dr. Anita Nair
Merck
Head of Regulatory Management- Pharma, Food Materials & Medical Devices
- Thời gian:
- 47 mins
- Ngôn ngữ:
- English
- Dữ liệu:
- 16 June 2026
Pharma and biopharma manufacturing, Cell Line Development
Next Generation CHOZN® Medium and Feeds
Our next generation medium and feeds platform is now available for testing and evaluation.
Jonathan Kaiser
Merck
Senior R&D Scientist, Process Materials and Cell Culture
Wilson Fok
Merck
Senior R&D Scientist, Process Materials and Cell Culture
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 10 June 2026
Pharma and biopharma manufacturing, Gene Therapy Contract Development and Manufacturing
Targeted LNPs: From Ligand Conjugation & Preclinical Screening to Process Optimization and Scale-Up
Johanna Simon, PhD
Merck
Head of Formulation Discovery & Analytical Characterization
Samaresh Sau
Merck
Principal Scientist
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 9 June 2026
Pharma and biopharma manufacturing, Cell therapy manufacturing
Release, redefined: QC testing across in vivo and ex vivo CAR-T
This webinar will highlight how quality control (QC) testing strategies for drug product evolve across both in vivo and ex vivo paradigms —focusing on identity, potency, sterility, and safety assays while introducing a new operating framework for fast, consistent ex vivo CAR-T release testing.
Leyla Diaz, Ph.D.
Merck
Technical Consultant, Scientific and Regulatory Consultancy
Kyle Reder
Merck
Segment Strategy Manager for Cell & Gene Therapy
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 2 June 2026
Pharma and biopharma manufacturing, Solid Formulation Strategies
Reduce dsRNA and optimize your IVT with our enhanced enzymes and high‑quality raw materials
Struggling with dsRNA or inconsistent IVT performance? Discover how enhanced enzymes and high‑quality raw materials can elevate purity, strengthen consistency, and raise the overall quality of your mRNA manufacturing.
Nelli Erwin
Merck
Strategic Product Manager
Oliver Prince
Merck
Senior Expert pDNA/mRNA/ GLP-1
- Thời gian:
- 1 hr
- Ngôn ngữ:
- English
- Dữ liệu:
- 28 May 2026
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