ISO 14155 Clinical Investigation Plan

ISO 14155 Clinical Investigation Consultancy program which involves Clinical Investigation Plan, Writing ISO 14155 documents, ISO 14155 Training, ISO 14155 Internal audit, ISO 14155 Clinical Investigation Standard Operating procedures, ISO 14155 Accreditation, ISO 14155

This part of ISO 14155 provides requirements for the preparation of a Clinical Investigation Plan (CIP) for the clinical investigation of medical devices. The compilation of a CIP in accordance with the requirements of this standard and adherence to it will help in optimising the scientific validity and reproducibility of the results of a clinical investigation.

This Standard does not apply to in vitro diagnostic medical devices.

Global Quality Services provides experienced staff to provide ISO 14155 consultancy, ISO 14155 Training, ISO 14155 certification, ISO 14155 documents, ISO 14155 Internal Audit. Drop a mail to This e-mail address is being protected from spambots. You need JavaScript enabled to view it and we will revert within in 2 working days.

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