Buckingham QA Consultancy

I have been a QA practitioner since 1990, with auditing experience in both CRO and Sponsor organisations. I am able to conduct data & report, system, study, facility or CRO audits on your behalf for GLP and VICH GCP related activities. I can also conduct audits of laboratories acting in support of GCP studies (GCLP).
I have experience in auditing dossiers, either whole dossiers for veterinary products or the safety section in dossiers for human pharmaceutical products. I also have some experience in auditing Phase IV clinical study reports and data.
I can assist in setting up and maintaining (and, if required, closing down) GLP compliant facilities, including laboratory, field and animal facilities.
I also offer training in GLP (including Study Director and multi-site study training), VICH GCP and GCLP.
I can offer practical advice and support in establishing minimum quality standards for facilities conducting non-regulated research.

Availability for Work

Remote, Worldwide

Areas of Expertise

Auditing, Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), Animal and Veterinary Products, Inspection Preparation, Standard Operating Procedures (SOPs), Quality Management Systems (QMS)

Contact Details

Sven Buckingham
Orchard View, 67d Cotmer Road, Lowestoft, Suffolk, NR33 9PS

Telephone: +44 (0)1502 517183

E-mail: svenbuckingham@hotmail.com

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