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 report, system, study, facility or CRO audits on your behalf for GLP and GCPV related activities. I can also conduct audits of laboratories acting in support of GCP studies.
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) and GCPV
I can offer practical advice and support in establishing minimum quality standards for facilities conducting non-regulated research.
Availability for Work
Areas of Expertise
GLP, GCP(Vet) and Field Studies
Orchard View, 67d Cotmer Road, Lowestoft, Suffolk, NR33 9PS
Telephone: +44 (0)1502 517183