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Maetrics helps you turn the challenge of regulatory and quality compliance into business improvements. Our expertise in medical device directives and standards means that we take a solution-based approach that is tailored to your needs and is fully compliant. With a wealth and depth of experience across sterile and non sterile devices, you can be confident that we will break the regulatory bottleneck, on time and on budget.

Maetrics can assist with:

CE Marking, 510(k), CMDCAS and other Worldwide Regulatory Compliance

Specific projects such as technical file authoring, sterilisation validation, internal auditing

Covering skills gaps

Filling knowledge gaps

Supporting growth into new markets

Supporting growth with new product lines

Specialist fields (Microbiology, Sterilisation, Risk Management, Clinical Evaluations and biological reviews)

Interim Cover (maternity, sickness, urgent need)

Resolution of Auditor findings

Global coverage – including USA, Canada, Australia, Europe and others

Training – both in-house and public courses provided

Candidate screening for regulatory and quality positions




BioCity Nottingham


Company Type

Lab and office



Clinical trial design, management & consulting Medical device Regulatory Affairs