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Explore new packaging solutions for life sciences, all in one convenient location at PACK EXPO East, March 18 – 20 in Philadelphia.

Lameplast: line of single, multidose containers and filling equipment at Pharmapack

Higher level of precision, functionality, and quality control with flexible closure design and printing capability as well as other features.

The vials offer a more attractive physical appearance (no burrs), uniform orifice/drug delivery, flexible closure design and printing capability, ability to mold with barrier materials vs. only one material, more uniform wall thickness, and reclosable features.
The vials offer a more attractive physical appearance (no burrs), uniform orifice/drug delivery, flexible closure design and printing capability, ability to mold with barrier materials vs. only one material, more uniform wall thickness, and reclosable features.

Lameplast, a Tekni-Plex business, introduces its line of plastic single and multidose containers, and filling equipment, for pharmaceutical/healthcare applications at Pharmapack, February 5-6, Paris Expo, Porte de Versailles, Paris, Booth E16.

The Lameplast system features pre-made vials that are designed to provide a higher level of precision, functionality, and quality control compared to blow/fill/seal systems. The vials offer a more attractive physical appearance (no burrs), uniform orifice/drug delivery, flexible closure design and printing capability, ability to mold with barrier materials vs. only one material, more uniform wall thickness, and reclosable features. These attributes are not possible to attain when the unit dose vial is blown, filled, and sealed in one stage, says the company. 

Lameplast will also be discussing its semi-automatic and fully automatic Pentafill fill/seal machines. Applications include pharmaceutical, diagnostic, medical device, veterinary, and cosmetic applications, with an emphasis on vaccines and ophthalmic medicine.

 The business unit’s quality management system is ISO 15378 and ISO 9001 certified. Lameplast is also a CE-mark holder for Class I medical devices, which indicates compliance with applicable European Union (EU) regulations and enables the commercialization of products in the 32 EU countries. Production is carried out in Class ISO 7 (Class 10,000) and ISO 8 (Class 100,000) controlled contamination environments according to ISO 14644-1.

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