GCP Auditing Services, independent consultancy and auditing in the area of Good Clinical Practice providing assurance of compliance with ICH and applicable regulatory requirements.With twenty years experience of auditing we can develop and deliver a complete auditing programme for you or simply help with specific elements. The Clinical Trial Directive now mandates inspections by regulatory agencies. Let us help prepare you for such an eventuality by carrying out a ‘mock’ inspection of your organisation. GCP Auditing Services, Good Clinical Practice, GCP audits, compliance, ICH, auditing programme, Clinical Trial Directive, regulatory agencies, mock inspection, pharmaceutical industry, Dr Harold Neal,, Quality Assurance, Education and Training Committee of the British Association of Research Quality Assurance (BARQA), Fellow of Research Quality Assurance (FRQA), Investigator site audits, ICH GCP, regulations, Phase I audits, Live phase audits, Regulatory Inspections, Clinical Trial Directive 2001/20/EC, Database Audits, CRFs, Clinical Report Audits, ICH GCP, Clinical Laboratory Audits, Audits of central clinical laboratories, Assessment audits of CROs, Independent audits of CROs, Training courses, Preparation of Standard Operating Procedures, Advice and preparation of SOPs
GCP Auditing Services, independent consultancy and auditing in the area of Good Clinical Practice providing assurance of compliance with ICH and applicable regulatory requirements.With twenty years experience of auditing we can develop and deliver a complete auditing programme for you or simply help with specific elements. The Clinical Trial Directive now mandates inspections by regulatory agencies. Let us help prepare you for such an eventuality by carrying out a ‘mock’ inspection of your organisation. GCP Auditing Services, Good Clinical Practice, GCP audits, compliance, ICH, auditing programme, Clinical Trial Directive, regulatory agencies, mock inspection, pharmaceutical industry, Dr Harold Neal,, Quality Assurance, Education and Training Committee of the British Association of Research Quality Assurance (BARQA), Fellow of Research Quality Assurance (FRQA), Investigator site audits, ICH GCP, regulations, Phase I audits, Live phase audits, Regulatory Inspections, Clinical Trial Directive 2001/20/EC, Database Audits, CRFs, Clinical Report Audits, ICH GCP, Clinical Laboratory Audits, Audits of central clinical laboratories, Assessment audits of CROs, Independent audits of CROs, Training courses, Preparation of Standard Operating Procedures, Advice and preparation of SOPs
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ABOUT US
GCP Auditing Services is an independent consultancy providing a range of services to the pharmaceutical industry in the area of Good Clinical Practice.

  It is operated by Dr Harold Neal, who has worked in the pharmaceutical industry in a Quality Assurance role for over twenty years. During that time he has conducted audits in almost every country in Western Europe as well as Central and Eastern Europe, India, South Africa, Australia and the United States.

He is a former member and chairman of the Education and Training Committee of the British Association of Research Quality Assurance (BARQA) and was previously the Treasurer of the Association. He was elected a Fellow of Research Quality Assurance (FRQA) in 2001.

 

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