High Edge Consulting, leading regulatory specialist to the medical device industry, will be at MEDTEC UK this year to support new and established medtech companies with compliance solutions that meet their practical operational and budgetary needs.
With their expertise and wealth of experience, High Edge offers medical device manufacturers and suppliers seven key service areas including: Regulatory Compliance, Quality Assurance, Contamination Control & Microbiology, Sterilization, Auditing, Training, EU Authorized Representative.
"With the ever changing regulatory landscape, the burden of compliance that medical device companies and their suppliers are facing is relentless and high on the corporate agenda, particularly with the Medical Device Directive recast and recent PIP scandal," comments Peter Rose, Managing Director of High Edge. He continues, "Having worked with over 50 medical device companies across Europe, the USA and Far East over the last eighteen months alone, at High Edge we realise the need to have compliance advice that you can trust, and balances practical support with the commercial aims of the business. This is what sets High Edge apart from the more traditional consultancy approach and means that we are at the cutting edge of medical device compliance."
At MEDTEC 2013 organisations can take advantage of the enhanced expertise offered by the High Edge team. Visit stand 321 to discuss all your regulatory and training requirements or to learn more about these industry leaders.