Medical Device Qualified Supplier Directory
Technimark Company Profile
Qualifications: ISO 13485, ISO 9001, FDA Registered, CGMP Certified, Supplier to Medical Manufacturers, Exhibitor in at least 2 MD&M and/or MEDTEC shows
Markets Supplied: Asia, North America, Central/South America, Europe
Technimark Healthcare offers consumer healthcare, medical and pharmaceutical companies fresh thinking, from product design and development to tooling and precision molding to assembly and pack out.
We’re relentless about bringing new ideas to every aspect of our operations. It’s how we’ve developed innovative, cost-effective solutions for leading brands for more than 30 years—and taken them from our advanced manufacturing facilities on three continents into hospitals, drug stores, doctors’ offices and patients’ homes. It’s innovation applied, around the world."
Whether you are manufacturing a diagnostic component, drug delivery device, medical product or a consumer healthcare package, Technimark is ready to assist you with the design and development of a comprehensive solution to address the needs of your simplest or most challenging programs.
Equipped with ISO-certified clean and white room environments, GMP Healthcare compliance, comprehensive IQ/OQ/PQ validation protocols and an experienced, multidisciplinary team of healthcare product manufacturing experts, we have you covered. Technimark is positioned to assist our clients to apply advanced technology-based solutions — spinning cube, high-cavitation, multi-shot, in-mold assembly and decoration, and post process automated assembly and decoration — that meet the stringent demands and regulations of the healthcare market. Leveraging our global footprint, we ensure that your products are made in the most cost-effective and logistically advantageous region for your needs.
The Capabilities which we provide to our customer are:
- New Product Design
- SIM’s (Scientific Injection Molding)
- Full Project Management
- Complete Part Validation (Installation, Operational and Performance Qualification)
- FDA Certified 21 CFR 820
- ISO 9001:2008
- ISO 13485:2003
- ISO 14001:2004 Environmental Management
- CE Marketing Certification for Class 1 Medical Devices
- Clean Room Manufacturing
- Advanced Engineering & Product Development
- Full In-House Metrology Capabilities
- Pad Printing and Value Added Services
- Insert and Over molding
- Sterile Packaging
Logistics (Inventory Management; Cross Docking and Kitting)
For more information contact Technimark