GCP Auditing Services
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Scan day: 12 February 2014 UTC
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Virus safety - good
Description: An independent consultancy providing auditing services for all aspects of clinical trials and good clinical practice.
!! GCP Auditing Services, GCP Audits, GCP auditor, independent GCP consultancy and GCP auditing in the area of Good Clinical Practice, ICH GCP regulatory requirements. GCP Auditing Services, GCP Audits, 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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| Page title: | !! GCP Auditing Services, GCP Audits, GCP auditor, independent GCP consultancy and GCP auditing in the area of Good Clinical Practice, ICH GCP regulatory requirements. |
| Keywords: | 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 |
| Description: | 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. |
| IP-address: | 193.151.16.129 |