Insights On Pharmaceutical Packaging
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2R Vials And Deep Cold Storage - Determining Mechanical & CCI Performance
8/27/2024
Review the implications of this study on the storage of sensitive molecules that require deep-cold storage and learn how 2R Fina glass vials are poised to enhance cold storage practices.
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PCI Pharma Services Capabilities Update January 2026: Fill/Finish
1/27/2026
Patricia Krainski highlights PCI’s global sterile fill‑finish and lyophilization strengths, showcasing investments that expand capacity, technologies, and integrated solutions for complex biologics, formulations, and lyophilized products.
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Improve Speed To Market By Mitigating Vial And Stopper Incompatibility
10/1/2024
These studies indicate that with a properly assembled vial containment system, good CCI performance can be achieved with stoppers of a given elastomer, independent of configuration/size, or vial style.
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Alba® Syringe Platform: Ensuring Stability For Sensitive Drugs
1/13/2025
Check out this exciting video showcasing the key advantages of Alba®: innovative coating technology that reduces potential interaction between the drug and container surface.
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Bottling Solutions
3/4/2025
Explore a bottling solution that is meticulously engineered to adhere to the most stringent pharmaceutical standards, which guarantees that each product is crafted with unparalleled quality and precision.
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FAQs On The Revised EU GMP Annex 1: Volume 1
3/5/2025
The revised GMP Annex 1 guidelines emphasize quality risk management, enhanced environmental monitoring, and data integrity, which aim to minimize contamination and ensure patient safety.
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New Standards For Elastomeric Components In Sterile Packaging
1/20/2026
USP’s new elastomeric packaging standards shift testing to full system‑level evaluation, strengthen integrity and usability expectations, and place compliance responsibility on drug developers.
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Overcome Common Pre-Filled Syringe Challenges Through Partnership
5/23/2025
The pre-filled syringe space is one of the fastest growing pharma sectors, offering greater patient safety and lower manufacturing costs. But pre-filled doesn’t translate to easily filled; there are particular obstacles to overcome.
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FAQs On The Revised EU GMP Annex 1: Volume 2
3/5/2025
Review the implementation of a holistic Contamination Control Strategy (CCS). Discover four key considerations for assessing component readiness: product, process, protection, and proof.
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Setup Made Simple With The BioTitan Retention Device
5/27/2025
Find out how quick and simple it is to set up an assembly secured with the Thermo Scientific BioTitan Retention Device.