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

For all your clinical auditing requirements ABOUT US SERVICES CONTACT HOME E-mail CONTACT For further information or to discuss your requirements please contact us By mail: 14 Reading Road, Farnborough, Hampshire GU14 6NA By phone: Tel: +44 (0)1252 519 359 Fax: +44 (0)1252 512 309 Mobile: 07792 278 458 By e-mail: info@gcp-auditing.co.uk   ABOUT US II SERVICES II CONTACT II HOME II E-mail GCP Auditing Services All text and imagery copyright GCP Auditing Services Information on this site is an overview of business and cannot be used to form part of a contract Terms and conditions on application Web site designed and hosted by Oast House Media