UPC Cambridge

ISO 13485 | Medical Devices Quality Management | MD 69713

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ISO 13485 | Medical Devices Quality Management | MD 69713

What UPC Offer

22 years of innovation, data & analysis creating wealth and IPR. Our services are:
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Product Consultancy
-Business Start-up services
-Patent support
-Managing innovation
-New Product Development
-Device services
-Regulatory Approval
-Product Industrialisation
Explore Further
Engineering Consultancy
- 1st principles Engineering
- New Product Development
- Drug delivery systems
- Sustainable life-cycle
- Root cause investigations
- Forensic investigation
- Testing and analysis
- Quality Strategy
Explore Further
New Product Development
- Project planning
- IP generation
- RMP, FTA, FMEA u,d&p
- Quality Strategy
- POP Models & Prototypes
- Predictive Modelling
- Design verification
- Approvals CE, CA, MDD, CFR
- Product Industrialisation
Explore Further
Drug Delivery Systems
- Medicines - treatment options
- Nasal Spray PDC
- Injectables & Inhalers
- Pumps - Patch & Syringe
- Disease Monitoring
- Regulatory approvals MDD
Explore Further
Sustainable Life Cycle Products
- Global warming potential
- Climate change
- Carbon life-cycle analysis
- Light-weight design
- Lower carbon emissions
Explore Further
Root Cause Analysis
- Novel design-led method
- FTA, FMEA
- Testing and analysis
- Predictive modelling
- Industrialisation review
- Quality Strategy
Explore Further
Ultra-Reliability QMS
- Experience derived QMS
- Ultra-reliable device method
- Embedded FTA, FMEA @ start
- Quality Strategy throughout
- Patient safety champion
Explore Further
Predictive Modelling
- UPC unique 6σ approach
- CTQ driven method
- Dimensional class by CTQ
- Function block models
- Stepping models - time, etc.
- Physics & Verification models
Explore Further
Forensic Witness
- Accident reconstruction
- Dispute resolution
- Patent, Trademark
- Civil versus Criminal
- Forensic investigation
Explore Further
Design Verification
- QMS ISO 13485:2016
- Testing capability
- Metrology (what is made?)
- Non-Destructive testing (meets specification?)
- Destructive testing (how robust is it?)
Explore Further

What UPC Offer

22 years of innovation, data & analysis creating wealth and IPR. Our services are:
Double Click Button

Product Consultancy
-Business Start-up services
-Patent support
-Managing innovation
-New Product Development
-Device services
-Regulatory Approval
-Product Industrialisation
Explore Further
Engineering Consultancy
- 1st principles Engineering
- New Product Development
- Drug delivery systems
- Sustainable life-cycle
- Root cause investigations
- Forensic investigation
- Testing and analysis
- Quality Strategy
Explore Further
New Product Development
- Project planning
- IP generation
- RMP, FTA, FMEA u,d&p
- Quality Strategy
- POP Models & Prototypes
- Predictive Modelling
- Design verification
- Approvals CE, CA, MDD, CFR
- Product Industrialisation
Explore Further
Drug Delivery Systems
- Medicines - treatment options
- Nasal Spray PDC
- Injectables & Inhalers
- Pumps - Patch & Syringe
- Disease Monitoring
- Regulatory approvals MDD
Explore Further
Sustainable Life Cycle Products
- Global warming potential
- Climate change
- Carbon life-cycle analysis
- Light-weight design
- Lower carbon emissions
Explore Further
Root Cause Analysis
- Novel design-led method
- FTA, FMEA
- Testing and analysis
- Predictive modelling
- Industrialisation review
- Quality Strategy
Explore Further
Ultra-Reliability QMS
- Experience derived QMS
- Ultra-reliable device method
- Embedded FTA, FMEA @ start
- Quality Strategy throughout
- Patient safety champion
Explore Further
Predictive Modelling
- UPC unique 6σ approach
- CTQ driven method
- Dimensional class by CTQ
- Function block models
- Stepping models - time, etc.
- Physics & Verification models
Explore Further
Forensic Witness
- Accident reconstruction
- Dispute resolution
- Patent, Trademark
- Civil versus Criminal
- Forensic investigation
Explore Further
Design Verification
- QMS ISO 13485:2016
- Testing capability
- Metrology (what is made?)
- Non-Destructive testing (meets specification?)
- Destructive testing (how robust is it?)
Explore Further