LIQUID DOSE FILLING
Mitigating Ultracold Storage And Transport Risk With CCIT
Dr. Derek Duncan, Director of Product Lines, Lighthouse Instruments, and Brandon Zurawlow, Chief Scientific Officer, CS Analytical, discuss a program for generating packaging data for deep cold storage products.
Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs
Check out this exciting video showcasing the key advantages of Alba®: innovative coating technology that reduces potential interaction between the drug and container surface.
Ensure Speed And Success With Your Drug Delivery Project
Hear from experienced professionals in the drug delivery space on how to ensure success and speed-to-market by establishing a firm foundation when working with a CMO.
How To Verify PFS System Performance
PFS system verification shouldn’t force a choice between diverting internal resources or investing in costly external testing. Explore a more efficient path that reduces complexity, cost, and uncertainty in performance validation.
EU Med Device Regulations: Ensuring Compliance For Integral Combination Products
Review the EU Medical Device Regulation (MDR) changes, specifically with respect to integral combination products, and examine the technical documentation packages supporting functionality and content.
Solutions In Pre-Filled Syringes For Biologics And Ophthalmic Applications
Discover how pharma companies can select tailored pre-filled syringes for biologics and biosimilars by aligning drug delivery needs with specialized containers and analytical services.
Early-Stage Considerations For The Selection Of Pre-Fillable Syringes When Developing A Vaccine
Get an overview of the strategy to speed up the migration from a vial to a pre-fillable syringe. Explore the main considerations in meeting and overcoming PFS-drug challenges when developing a vaccine.
A Data-Driven Approach To Container Closure Integrity
Gain confidence in your container closure system selection by utilizing a stepwise and data-driven approach to predicting and verifying container closure integrity.
CCI Testing And Revisions To EU Annex 1
The new language in EU Annex 1 will likely have a significant impact on your CCI testing practices. In this webinar CCI testing strategies and the proposed revisions to EU Annex 1 are discussed.
The Successful Implementation Of A New Aseptic Filling Line
Discover how a Quality by Design approach can streamline the development of new sterile product filling lines, featuring a real-life example illustrating its effectiveness.
Determining And Controlling Oxygen Levels In Sensitive Formulations
This webinar will review how oxygen levels in finished parenteral drug containers can be determined and controlled throughout the product life cycle by using laser-based headspace analysis.
Redefining Prefillable Syringe System
See how our Synchrony S1 pre-fillable syringe system delivers an integrated, system-level solution designed for performance, quality, and scalability — with simplified submissions, synchronized supply, and compatibility across the drug delivery ecosystem.
Driving Excellence In Aseptic Fill-Finish: A Strategic Partnership With Stäubli Robotics
See how intelligent automation and purpose-built robotics deliver contamination control and operational excellence in demanding sterile manufacturing environments.
Consistent, Reliable, High-Quality Components
Discover a premium line of components for vials, prefilled syringes, and cartridge systems developed and refined to provide best-in-class levels of quality, performance, and risk mitigation.
Protecting Your Drug Product
With patient lives depending on every dose, even minor vulnerabilities in containment or delivery systems can have serious consequences for product integrity and patient outcomes.
EZ-fill® Kit: RTU Packaging Solutions For Fast Access To Small Volumes
Discover the EZfill Kit in action—an innovative solution designed to streamline and enhance precision in liquid handling, optimizing efficiency for pharmaceutical and bioprocess applications.
Streamline Your Path To Clinical Fill
Drug-independent PFS testing is a required early step — but it can be time-consuming and resource-intensive. What if you could eliminate the effort without losing the data you need?
Efficient, Single-Source PFS Supply
When component lead times don’t align, inventory piles up, cash gets tied up, and forecasts can quickly turn into waste or shortages. What if a single integrated PFS system could simplify it all?
Using Positive Controls In Container Closure Integrity Studies
This webinar describes the use of positive controls as an important element of CCI studies designed to validate packaging components for CCI or to qualify processes for producing good CCI.
Start With An Integrated, Verified PFS System
Synchrony S1 PFS system delivers an integrated, verified solution designed to streamline submissions, support reliable supply, and reduce development risk.
Streamline Global Regulatory Submissions
Discover a more streamlined approach with one accountable partner supporting regulatory submissions globally.
Mycap® Bottle Closures – Aseptic Fluid Transfer Systems For Bottles
The innovative MYCAP bottle closure system provides more options for aseptic fluid transfer in bottles and rigid containers. The elastomeric closure makes it a truly universal closure system.
Selecting A Prefillable Syringe System With Confidence
Discover an advancement in the prefillable syringe market, uniquely integrating the syringe barrel, plunger, and needle shield/tip cap into a fully harmonized, verified system from a single supplier.
Selecting Container Closure Components: Extractables And Leachables
Primary packaging components require a thorough assessment to ensure safety and efficacy. Plan ahead and start your assessment early to mitigate your risks, delays, and out-of-pocket costs.
Accountability For The Whole PFS System
When component suppliers only own their part, system-level performance becomes your responsibility. And if something fails, accountability disappears into the gaps.
Minimizing Particulate Risk
While visible particles often draw immediate attention, visual inspection alone is insufficient, as subvisible particulate matter can pose equally significant risks to patient safety.
EZ-fill Smart™ Enhancing Aseptic Fill-Finish Efficiency In Pharmaceutical Manufacturing
Discover how the EZ-fill Smart system, integrated with Groninger technology, enhances aseptic fill-finish processes, improving efficiency, sterility, and scalability in pharmaceutical manufacturing.