Comprehensive quality management and regulatory compliance for your device

We maintain a Quality Management System to control the design, development and manufacturing processes for products entering into worldwide markets

This system incorporates appropriate quality gates throughout the design and manufacturing process from supplier selection and qualification, through to final acceptance, device tracking and device maintenance.

Integrated Technologies Ltd is accredited and audited to:

Our quality system additionally incorporates BSEN ISO 14791, BSEN 62304 and BSEN 62366, amongst others, to ensure a fully compliant regulatory framework.

ITL works closely within the appropriate European CE marking directives including:

  • 93/42/EEC Medical Device Directive
  • 98/79/EC In-Vitro Diagnostics Directive
  • 2006/95/EC Low Voltage Directive
  • 2004/108/EC Electromagnetic Compatibility Directive
  • 2011/65/EU RoHS II Directive

Medical device regulatory consultancy

We also offer medical device development and regulatory consultancy, including pre-compliance safety and regulatory assessments, to assist you in your medical device product development project.

We have considerable experience in supporting our customers to achieve American Food & Drug Administration (FDA) 510k and Pre-Market Approvals (PMA).

Our Chinese facility also facilitiates China Food & Drug Administration (CFDA) applications.

Furthermore, we can help you to manage submissions and on-going factory audits for Nationally Recognised Testing Laboratories (NRTLs) including UL, CSA, ETL and MET (for US and Canadian market approval).

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News
ITL Group Celebrates 22nd Year Exhibiting at MEDICA Trade Fair

Leading medical device design and manufacturing company, ITL Group (a Gooch & Housego Company) returns to the MEDICA tradeshow in Düsseldorf, Germany this November for its 22nd year.

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Resource
Quotation for Manufacturing Checklist

ITL Group is the trusted design and manufacturing partner for leading medical technology, in vitro diagnostic devices and analytical instruments. This handy infographic provides an overview of some of the project critical documentation and processes required to get your device into production.

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Case Study
DAME

Design Transition of a Reusable Tampon Applicator from Concept to Rapid Tooling

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Case Study
LumiPod

A complete R&D project to develop a demonstrator of the technologies that will be incorporated in future Point-of-Care (POC) devices

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