Our Services

Waste Management Solutions

  •  Feasibility appraisals and analysis of waste minimization, collection, treatment and waste disposal solutions
  • Waste Master planning: Scheme master planning for waste treatment and waste disposal facilities;
  • Planning & Permitting: Waste facility planning, environmental impact assessment and permitting;
  • Procurement: Development of waste service procurement strategy and waste contract bid support;
  • Energy: Advice on energy recovery.
  • Urban Regeneration: Waste strategy for commercial, residential and industrial development from small scale construction projects to major urban regeneration;
  • Infrastructure: Waste treatment infrastructure design including
    • Civic amenity sites
    • Waste transfer stations
    • Materials recycling/recovery facilities
    • Mechanical and biological treatment facilities
    • Anaerobic digestion facilities
    • Mechanical heat treatment facilities
    • Composting facilities
    • Advanced thermal treatment facilities
    • Inert, non-hazardous and hazardous waste residual landfills;
  • Process Design: Waste treatment process design and layout;
  • Project Management: Waste facility operational commissioning and training.

Medical Waste Consulting

P&O Advisory Services – Medical Waste Equipment

P&O delivers comprehensive regulatory services to help get your product into the International medical market. You can choose elements of our service or take advantage of our experience to enhance your product development and strategy, your CE Marking and your ISO 13485 quality management system.

Our experienced project consultants can help plan your projects, help predict pitfalls and hurdles, and use their knowledge to indicate which project activities require early attention. Our experienced engineers can assist in product design and implementation. Our regulatory consultants can get you through the red tape. We have experience designing and operating systems to comply with ISO 9000, ISO 13845 and TS 16949.

Medical Quality Systems, Regulatory Compliance, Design Control and Validation

Elements to address when developing your product and producing a Technical File or 510k Submission

  • Development Project Management
  • Standards review
  • Product design
  • Test early prototypes
  • Statement of Claims
  • Essential Requirements Check List
  • Risk Analysis (ISO 14971)
  • Functional testing protocols and test reports
  • Biocompatibility testing
  • Sterilisation validation
  • Drawings, specifications, BOM (bill of materials) and supplier audits
  • Training

Quality Management Systems

  • Process analysis
  • ISO 13845 Documentation
  • ISO 13845 Pre-Audit
  • Internal Auditor training
  • Process implementation


  • Advice on how to apply ISO 10993 and in-vivo functional tests, and when to use material characterisation chemical tests in place of lengthy toxicity testing

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