June 2011 Editor's Picks: Products from Meissner and Telstar - Pharmaceutical Technology

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June 2011 Editor's Picks: Products from Meissner and Telstar

Equipment and Processing Report

Featured products from Pharmaceutical Technology's monthly newsletter, Equipment & Processing Report

product Meissner
Filter system reduces cleaning requirements

Meissner’s inline UltraCap H.D. assembly is a ready-to-use, integrally sealed filter and housing system. The system’s filter element is welded into a disposable polypropylene housing unit to form an assembly without O-rings. The assembly’s absence of O-ring materials and its construction from natural polypropylene material help reduce extractables and leachables.

The UltraCap H.D. assembly is completely disposable, thus reducing cleaning and cleaning validation costs and enabling faster and more convenient change-outs than traditional cartridge and filter housing systems. In addition, the inline capsule filter was designed to withstand higher temperatures and operating pressures than conventional high-capacity capsule filters. The unit’s inline flow configuration is intended to provide high flow rates by reducing housing pressure loss.

The UltraCap H.D. filter is available in lengths from 10 to 50 in. and pore sizes ranging from 0.04 through 99 µm. Users can choose the new inline version or the existing T-style version of the system depending on their requirements.


productTelstar
System loads and unloads lyophilized vials

Telstar’s new automatic vial-loading and -unloading system operates under aseptic conditions and is compatible with conventional cleanroom and barrier technologies. The vial-loading technology incorporates mechanisms driven by a set of three flexible, curved steel bands that make it compact and easy to clean. The entire system is situated outside the lyophilizer when not in active use. The lateral curvature of the bands gives them high stiffness, which reduces requirements for guidance and makes system elements accessible for cleaning.

The system can be configured in a pass-through layout that makes it possible to segregate loading and unloading in areas in terms of aseptic classification and degree of operator protection. The system integrates easily with isolators designed to separate operators from toxic chemicals. Under isolated conditions, operators can access all working areas easily and safely using gloves for activities such as changes of format and sampling.

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Better Comms Means a Fitter Future for Pharma, Part 1: Challenges and Changes
Source: Equipment and Processing Report,
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