Accelerated aging
A test method (ASTM F1980) that stores sterile packaging at elevated temperature to predict real-time shelf life in a shorter period, used to support expiry-date claims.
A test method (ASTM F1980) that stores sterile packaging at elevated temperature to predict real-time shelf life in a shorter period, used to support expiry-date claims.
A multilayer material with an aluminium layer that provides an near-absolute barrier to moisture, oxygen and light — standard for pharmaceutical blister lidding and high-barrier pouches.
A film engineered to restrict the transmission of gases, moisture or aromas, characterised by its oxygen (OTR) and water-vapour (WVTR) transmission rates.
A format in which a product sits in a pre-formed plastic cavity sealed to a lidding material (foil, film or board). Common in pharma and consumer goods for unit-dose dispensing and tamper evidence.
A package-integrity test (ASTM F1140/F2054) that inflates a package until the seal fails, measuring the pressure the weakest seal can withstand.
A hinged blister pack where the top and bottom halves are formed from the same sheet and fold together. Common in retail for tools and hardware.
A process that combines multiple polymer layers into a single film in one step, letting each layer contribute a property such as barrier, strength or sealability.
Packaging with thermal insulation and phase-change materials (PCM/VIP) that keeps temperature-sensitive products within a defined range during storage and transport.
A seal-leak test (ASTM F1929) in which a dye solution is applied to a seal; capillary movement of the dye reveals channels or defects.
Ethylene vinyl alcohol — a polymer with an excellent oxygen barrier, used as a thin inner layer in coextruded barrier films.
Non-rigid packaging made from films, foils and laminates — pouches, bags and wraps — valued for low material use, printability and light weight.
A horizontal form-fill-seal (HFFS) process that wraps a product in a continuous film tube with a longitudinal fin seal and two end seals. Also called flowpack.
An automated process that forms packaging from film, fills it with product and seals it in one continuous line. Exists as vertical (VFFS) and horizontal (HFFS) systems.
The lower web in a thermoforming line that is heated and shaped into cavities to hold the product before the lidding film is sealed on top.
Horizontal form-fill-seal — an FFS layout where product moves horizontally; the basis of flow-wrap and many tray/pouch lines.
A bond created by applying heat and pressure to fuse two thermoplastic surfaces, forming the primary closure in most flexible and thermoformed packaging.
The international standard for packaging of terminally sterilized medical devices. Part 1 covers materials and sterile barrier systems; Part 2 covers process validation.
The upper web sealed onto a thermoformed or pre-made tray/blister to close it, often peelable and printed.
The ability of a packaging material to prevent the ingress of microorganisms, essential for maintaining sterility (tested per ASTM F1608).
Replacing the air inside a sealed pack with a controlled gas mix (typically N₂, CO₂, O₂) to extend shelf life without preservatives.
The amount of oxygen that passes through a film per unit area and time — a key metric for barrier and shelf-life performance.
A glycol-modified PET copolyester with good clarity and formability, widely used for thermoformed trays, blisters and medical packaging.
A seal designed to open cleanly by hand without tearing the material, giving controlled, aseptic access — important for medical and food packs.
The force required to separate a seal (ASTM F88), balancing package integrity against openability.
The tooling that applies heat and pressure in a defined pattern to create seals; its geometry determines seal width, strength and appearance.
The period a product remains fit for use in its packaging under defined storage conditions — validated through real-time and accelerated aging.
Wrapping a product in film that contracts around it when heated, consolidating or protecting single items or multipacks.
Vacuum skin packaging draws a heated top film tightly over a product on a rigid base, forming a second-skin vacuum pack that extends shelf life for fresh foods.
The minimum packaging that maintains sterility of a medical device to the point of use — the core concept of ISO 11607.
Packaging designed to reduce environmental impact through recyclable, recycled, bio-based or reduced materials while maintaining performance.
Heating a plastic sheet to its forming temperature and shaping it against a mould under vacuum, pressure or plug assist to create trays, blisters and cavities.
Applying a lidding film to a pre-formed tray with heat and pressure to create a sealed, often MAP or vacuum, pack.
A spunbonded high-density polyethylene material (DuPont) that provides a microbial barrier while allowing gas sterilisation — the standard porous web for sterile medical packaging.
Vertical form-fill-seal — an FFS layout where film is formed into a vertical tube, filled from above and sealed; common for granular and bulk products.
Removing air from a pack before sealing to slow oxidation and microbial growth and to reduce volume.
The amount of water vapour passing through a film per unit area and time — a key metric for moisture-sensitive products.
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