E&O Laboratories Ltd

• Health Products Regulatory Authority, Medical Devices Department
  IrelandContact the authority →

No certificates registered for this manufacturer.

Devices placed in 1 country

• Ireland20

2 contacts identified

• CC
  CAMERON Clare

  PRRC
  View profile →
• CAMERON Clare
  Person responsible for regulatory compliance in accordance with article 15 of IVDR. Management of IMS in compliance with IVDR, ISO 13485, ISO 9001, ISO 17025 & customer requirements. Report effectiveness of the IMS. Promotion of regulatory, quality and customer awareness across the business. Managing the release for sale and disposition of products. Managing the QA and Laboratory departments. Managing the audit programme, post market surveillance, CAPA, risk management and third party inspection
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• Syntec Scientific Ltd — represents — E&O Labs
• CAMERON Clare — E&O Labs