Quality Assurance and GCP Auditing of Clinical Trials & Systems

 

CRC Clinical research Consultancy Ltd. is owned and managed by Sarah Elbaz.

The company was established as an International consultancy providing a full range of independent CRA and Good Clinical Practice (GCP) Quality Assurance audit services on a global basis.

 

CRC aims to provide cost-effective, timely project custom solutions and services to leading Pharmaceuticals, Medical Device, Biotechnology and CRO companies.

Service include Investigational site GCP audits, Quality Systems Audits for CROs – Monitoring, Project Management, Data Management and CRO Oversight, Phases I-IV audits, Mock inspections and SOP development as well as local and international regulations, study planning and milestones.

CRC also has extensive knowledge and experience in developing, designing, training and implementation of EDC (Electronic Data Capture/eClinical expertise).

 

CRC Ltd. is fully committed to the client with professionalism as a fundamental business principle. The core of the process is achieving customer satisfaction by employing knowledge and experience. CRCs philosophy is to offer excellence, integrity and reliability of performance in a straightforward, client-focused way – to create and maintain partnerships with customers; to provide client-oriented service at professional expert level applying high ethical standards; to ensure that my efforts are a profitable experience to my clients; and to be recognized by client as a trusted partner.

 

I believe that integrity and trust, experience and expertise, customer-oriented flexibility and truly personal service are the keys for success. CRC embodies these values on every mission.

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Sarah Elbaz