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LIQUID DOSE FILLING

1:10:50 Determining And Controlling Oxygen Levels In Sensitive Formulations
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.

41:44 stevanato 1
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.

56:16 QT Podcast with Andy
Quality Time With Oliver: Guest - Andy Goll

Blow-fill-seal technology enables custom single-dose liquid packaging for surgical applications, accommodating viscous liquids, emulsions, and suspensions that standard formats cannot handle.

49:20 Using Positive Controls In CCI Studies
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.

1:05:10 CCI Testing And Revisions To EU Annex 1
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.

2:37 alba platform
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.

0:22 Level performance
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.

2:30 West-Feature-PFS SYRG-0178 NovaPure
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.

1:00:45 730A2315_1ST PASS (1)
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.

1:06:57 West-SPO 3 - GCApp_LCMSQof
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.

4:13 Driving Excellence In Aseptic Fill-Finish
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.

1:01:23 1mL_Standard_Group_Glove copy
From Complexity To Confidence In Prefillable Syringe Transfer

Discover how aligning packaging strategy with technology transfer requirements can accelerate timelines, control costs, and support successful injectable drug product manufacturing.

0:20 Streamline Your Path To Clinical Fill
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?

48:38 Vaccine Vials GettyImages-1316775813
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.

2:50 ez smart fill
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.

0:25 Streamline Global Regulatory Submissions
Streamline Global Regulatory Submissions

Discover a more streamlined approach with one accountable partner supporting regulatory submissions globally.

1:27 Redefining Prefillable Syringe System
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.

2:20 Mycap Bottle Closures
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.

1:51 EZfill Kit
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.

0:23 Minimizing Particulate Risk
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.

1:07:34 Vials GettyImages-116406654
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.

0:24 Protecting Your Drug Product
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.

0:26 Efficient, Single-Source PFS Supply
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?

1:04:31 The Successful Implementation Of A New Aseptic Filling Line
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.

1:28 Start With An Integrated, Verified PFS System
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.

50:18 West-SBO 1 - GC_APP_3e FunShot_4
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.

0:25 Accountability For The Whole PFS System
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.

59:47 Early-Stage Considerations For The Selection Of Pre-Fillable Syringes When Developing A Vaccine
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.

47:10 West-SPO 2 - GC_App_PFS RNEDS-037
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.