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Injecting innovation into micro-injection molded solutions

12 Mar 2019

End-to-end industrial production of innovative medical technology products.

Using its internal expertise, Weidmann Medical Technology develops primary packaging for pharmaceutical plastic containers, enclosures for fluid and solid medications with safety components, as well as drug delivery systems for international pharmaceutical companies.

The company's pharmaceutical product range includes the following:

  • Housing for aelf-Injectors: multicomponent molding for self-injector systems, with a user-friendly soft tip area.
  • Needle Shields: with integrated anti-needle injury technology - a specially developed 'TPE' for a new generation of needle shields. Mass production with highly complex multicavity molds.
  • Rigid Caps: modern, multipart sealing system for pre-filled syringes with intuitive screw-cap mechanism consisting of rubber cap, rigid cap and Luer-Lock-Adapter.

  • As a specialized one-stop shop, Weidmann Medical Technology can assure customers with its portfolio of core competencies:
  • Rapid prototyping, rapid tooling, 3D printing, high complexity molds
  • High multicavity tooling, multi-component molding (up to 3), insert-molding
  • Scientific injection molding
  • Chemical and physical joining technologies (glueing and welding)
  • Semi- and fully automatic assembly lines with qualified in-line vision control systems
  • Various printing and labeling technologies such as thermotransfer, stamping and pad-printing; laser and inkjet printing
  • Design for manufacturing and assembly in-line and off-line primary packaging (i.e. thermoforming)
  • Manual and fully automated secondary packaging systems.

  • To ensure confidence and customer products make the successful journey from drawing board to market, Weidmann has taken the necessary steps to gain various 'quality' certification/status:
  • Certified ISO 13485
  • FDA-listed to CFR820 standards
  • Project and manufacturing processes to cGMP standards
  • Supply risk mitigation and emergency planning
  • Fulfillment of SHE, ROHS and REACH standards
  • Risk management acc. ISO 14971
  • Integrated CAPA and change control systems
  • DQ, IQ, OQ, PQ qualifications and validations
  • Software validation to FDA, Part 11 standards
  • Design history files, device master records.

  • Visitors at this year's CPhI Worldwide event can meet Weidmann at Innopack, Stand 6G43.

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