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Development and manufacture of sterile packaging solutions and contract packaging for medical technology and pharmaceuticals.

Früh Logo

Früh Verpackungstechnik AG

Fehraltorf (Headquarters/Production) · Exton, PA (USA, North America)New on Amplifa

1980Founded
650Employees
2Locations (Switzerland, USA)
ISO 7 / ISO 8Cleanroom classes
ISO/IEC 17025Accredited laboratory

About Früh Verpackungstechnik

Früh Verpackungstechnik AG is a Swiss industrial company based in Fehraltorf that develops and produces packaging solutions for the medical technology and pharmaceutical industries. The offering includes the development and manufacture of packaging materials such as films, pouches, blisters and trays, including those made from Tyvek and functional multilayer films, which are produced using laminating and finishing processes. In addition, the company offers contract packaging for medical devices and pharmaceutical products under cleanroom conditions according to ISO 7 and ISO 8, including assembly, labeling, cartoning, serialization and case packing. Since 2026, Früh has been building an approximately 900 m² assembly and packaging line for autoinjectors with cold-chain capability. The service portfolio is complemented by engineering services (CAD design, prototypes), validations in accordance with Swissmedic GPA guidelines, sterilization services, and a laboratory accredited to ISO/IEC 17025. Founded in 1980 by Albert Früh, the family-run company employs around 650 staff and also serves the North American market through its Exton (Pennsylvania, USA) location.

Site
Fehraltorf
Processes
Blister/tray packaging development and production for medical devices and pharmaceuticals, Film and pouch packaging (Pouches), Contract packaging medical technology (Contract Packaging Medical), Contract packaging pharmaceuticals (Contract Packaging Pharma), Autoinjector assembly and packaging (Assembly, Labeling, Cartoning, Serialization, Case Packing), Laminating and finishing processes for functional multilayer films (lamination), CAD-based packaging development and prototype construction, Sealing process qualification and validation (Sealing)
Materials
Tyvek, Film/Films, Multilayer films/composite materials, Films
Certificates
ISO/IEC 17025 (accredited laboratory services), ISO/IEC 17025 (laboratory accreditation), GMP qualification standards, Cleanroom ISO 7 / ISO 8
Founded
1980
Employees
650
Industries
Medical Technology, Pharmaceutical Industry
  1. 01

    Engineering (design, CAD, prototypes)

  2. 02

    Material selection and testing

  3. 03

    Packaging material production (films, pouches, blisters/trays)

  4. 04

    Contract packaging/assembly under cleanroom conditions

  5. 05

    Validation and qualification

  6. 06

    Laboratory analyses and stability tests

  7. 07

    Sterilization validation and support

  8. 08

    Delivery

Materials and Processes

TYVEK

Tyvek

Porous sterile barrier material for blister lids and sterile packaging of medical devices.

Folie

Films

Base material for pouches, blisters and trays in pharmaceutical and medical technology packaging.

Verbund

Multilayer films/composite materials

Functional multilayer films produced by laminating and finishing processes for high barrier requirements.

Locations

Fehraltorf

CH

Headquarters and production

Materials
Tyvek, films, multilayer films
  • Magna-Mike 8600 wall thickness gauge
  • Assembly and packaging line for autoinjectors (approx. 900 m², under construction 2026)
  • Cleanroom ISO 7 / ISO 8
  • Testing laboratory (accredited to ISO/IEC 17025)

Exton, Pennsylvania

US

North America location (Fruh Packaging Inc.)

Industries

Medical TechnologyPharmaceutical Industry

Processes & technical limits

ProcessesToleranceMax. partWeightLot sizeMaterials
Blister/tray packaging development and production for medical devices and pharmaceuticalsPlastics––––Film, Tyvek
Film and pouch packaging (Pouches)Plastics––––Film
Contract packaging medical technology (Contract Packaging Medical)Assembly–––––
Contract packaging pharmaceuticals (Contract Packaging Pharma)Assembly–––––
Autoinjector assembly and packaging (Assembly, Labeling, Cartoning, Serialization, Case Packing)Assembly–––––
Laminating and finishing processes for functional multilayer films (lamination)Plastics––––Films, Composite materials
CAD-based packaging development and prototype constructionEngineering–––––
Sealing process qualification and validation (Sealing)Joining–––––
Dye Penetration Test for porous packaging ASTMF1929Testing––––porous packaging
Dye Penetration Test for non-porous packaging ASTMF3039Testing––––non-porous packaging
Bubble Emission Test ASTMF2096 / ASTMD3078 (overpressure/vacuum chamber)Testing–––––
Visual inspection of seal seams ASTMF1886/F1886M Part 1Testing–––––
Visual evaluation of primary packaging ASTMF1886/F1886M Part 2Testing–––––
Oxygen transmission rate testing (OTR) ASTMF1927 / ASTMD3985 / ISO15105-2 / DIN53380-3Testing––––Films, Composite materials
Wall thickness measurement Magna-Mike 8600 (Hall effect)Testing–9.14 mm material thickness––non-magnetic materials
Seal seam strength testing ASTMF88/F88MTesting––––flexible barrier materials
Tensile strength and elongation at break testing DIN EN ISO 527-1/-3Testing–1 mm material thickness–––
Puncture resistance testing DIN EN 14477 / ASTMF1306Testing–––––
Linear dimensional measurement of packaging (ruler ASTMF2203, caliper, resolution 0,01 mm)Testing0,01 mm (measurement resolution)––––
Climate tests and climate change tests (e.g. ASTMD4332)Testing–––––
Stability tests / accelerated aging ASTMF1980Testing–––––
Performance tests e.g. ASTMD4169 or ISTA3Testing–––––
Sterilization validation radiation sterilization (gamma and X-ray) according to EN ISO 11137Heat Treatment–––––
Steam sterilization and EtO sterilization validation support (EN ISO 17665 / EN ISO 11135)Heat Treatment–––––
Microbiological monitoring (bioburden, organism identification, endotoxin testing ISO 11737)Testing–––––
Packaging of products under ISO 7 cleanroom conditionsAssembly–––––
Packaging under controlled cleanroom conditions ISO 7 and ISO 8Assembly–––––

2 Anlagen & Maschinen

MachineManufacturer / modelQuantityWorking areaYear builtSite
Magna-Mike 8600 wall thickness gauge (Hall effect)Magna-Mike 8600–Wall thicknesses up to 9.14 mm on non-magnetic materials–Fehraltorf, Switzerland
Assembly and packaging production line for autoinjector (Assembly, Labeling, Cartoning,–1approx. 900 m², three packaging configurations, Cold Chain2026 (imFehraltorf, Switzerland

Additional services

Packaging material production (films, pouches, blisters/trays)Contract packaging medical technology (Contract Packaging Medical)Contract packaging pharmaceuticals (Contract Packaging Pharma)Engineering services (design, CAD, prototypes)Validation services (hygiene, process, product, sterilization)Sterilization services and microbiological monitoringAccredited laboratory analyses and tests (ISO/IEC 17025)Qualification standards (GMP)Assembly and packaging (e.g. autoinjector line)Serialization

Quality and Accreditation

Früh operates a laboratory accredited to ISO/IEC 17025 for integrity, material and climate tests (e.g. ASTM F1929, F88, F1980). Packaging is performed under ISO 7/8 cleanroom conditions; validations are carried out in accordance with Swissmedic GPA guidelines and standards such as EN ISO 11137.

EvidenceFehraltorf
ISO/IEC 17025 (laboratory accreditation)
GMP qualification standards
Cleanroom ISO 7 / ISO 8

History

  1. 1980

    Albert Früh founded Früh Verpackungstechnik AG in Fehraltorf.

  2. After a seamless generational transition, a six-member management team (Hans-Peter Früh, Thomas Good, Christoph Marty, Regina Bruggisser, Robert Sedlic, Yasin Gencel) runs the company with around 650 employees.

  3. 2026

    Construction of a new assembly and packaging line for autoinjectors (approx. 900 m², cold chain, three packaging configurations).

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