Compare like-for-like
Align quoted sites, activities and assessment cycles. Separate audit, decision, travel and additional-control charges. Base prices may not represent annual cost.
Internal staff time
Duplicate entry and reconstructed records create costs. Shared registers can help while retaining traceability and responsibility.
Plan changes
Review new products, sites and contracts before implementation. No guaranteed savings percentage is promised without business data.
What the project produces
The agreed scope includes a requirements map, prioritised actions, responsibilities, operating records and a readiness review. Deliverables are agreed before implementation. Existing documents are reviewed for usefulness rather than replaced automatically.
Evidence before the review
Prepare process descriptions, supplier records, traceability information and any open findings. Do not send sensitive files through the public contact form. The first enquiry should describe the operation; detailed document exchange is agreed separately.
Frequently asked questions
Does QAP issue certificates?
No. Certification decisions belong to the relevant authorised bodies.
What is needed to start?
Products, activities, sites, current records and your target date.
Can we work remotely?
Document work can be remote. Site-review needs depend on scope.
Does a template prove compliance?
No. Records and actual practices must support implementation.
Is certification guaranteed?
No. Assessment evidence and the certification body determine the outcome.
How is the advisory fee calculated?
Individually, based on scope, sites, available evidence and timeline.