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Harrison Clinical Research GmbH

Harrison Clinical Research
Albrechtstrasse 14
80636 Munich, Germany
Tel: 49-(0)89 - 12 66 80-0
Fax 49-(0)89 - 12 66 80-2444
Homepage: www.harrisonclinical.com

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The Successful Preparation of FDA-GCP Inspections

Harrison Clinical Research will be hosting an event entitled “The successful preparation of  FDA-GCP inspections”.

This event is scheduled to be held on Thursday, March 25th 2010 at the offices of Harrison Clinical Research France SAS, 3 rue Bellanger, 92300 Levallois-Perret. It will be presented in English by Dr Barbara Schnurr, Quality Management Director. Dr Schnurr is a regular presenter and chairperson at international meetings on Quality Assurance and Quality Management, building up a tremendous reputation in this area and she is the author of many QA related publications.

Harrison Clinical Research is an international, full-service CRO with hands-on experience in auditing and quality management. Since 1996, we have audited ca. 500 studies carried out in more than 20 countries. Our auditors have a broad range of experience in clinical research and specific audit experience in: system audits and on-site audits, as well as audits of Phase I units, analytical and clinical laboratories, medical device studies, data management, electronic data capture and qualification records/training documents.

We provide a large range of diverse quality management services including:

  • Preparation for FDA Inspection, EMEA Inspection, local Competent Authorities Inspection 
  • Quality auditing services
  • Guidance in setting up and implementing QM services; gap analysis for existing QM systems
  • Advice on minimum requirements for SOP systems; writing, reviewing, updating and adapting SOPs
  • Quality training services

If you are interested in learning more about our services, please have a look at the sub-section "Quality Assurance and Auditing" in the "Services" section of this website and please do not hesitate to contact us. We would be happy to answer any questions you may have.

Programme and Registration - The Successful Preparation of FDA-GCP Inspections

Please note that the event is FREE OF CHARGE.
Certificates of Attendance will be given to all participants.
We look forward to receiving your registration.

Jean-Michel Paillarse,
Business Development Director,
Harrison Clinical Research France SAS

2010, February