Whether your objective is CE marking, FDA submission, benchmarking or marketing-support
data, we can assist you. Our laboratory isrun by engineers with a minimum of 15
years experience in the medical device industry. We can participate in your Risk
Analysis and process FMEA (Failure Mode Analysis) to ensure that bench testing
is provided to correctly support your product claims. Where necessary, we support
bench testing with in vivo functional studies and clinical trials.
- Product functionality
- Verification of key product claims
- Risk analysis challenge
- Independent investigation of customer feedback
- Comparative studies
For further information and advice, please call us on (0)8454 588924 or E-mail:
Recent projects include:
- Measurement of filtration efficiency
- Proving the effectiveness of sterility barriers
- Coupling functionality
- Bonding strengths
- Leak and flow studies
- Simulated use and ease of use
- Package accelerated ageing studies
- Package integrity and seal strength studies
- End user complaints analysis
- Competitor comparisons
- Wound dressing antimicrobial and haemostasis studies
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