Who are we?
Steve Hewitt set-up Sanbec Consulting after retiring from the Pharmaceutical industry in 2012.
Sanbec Consulting (SC) has wide experience of auditing and training in the pharmaceutical industry, gained by working in major pharmaceutical companies for over 30 years.
With our associates, we are able to offer experience and expertise of more than 100 years in the pharmaceutical industry. Having worked at director level all staff are professionally qualified and currently belong to several working committees relating to GMP, GDP, Parenteral drugs and Excipients.
Our clients include regulatory agencies, many global pharmaceutical companies and suppliers to the industry (both large and small), with contracts lasting from a few days to six months in duration.
SC can provide support in many areas and are able to call on their specialist associates as required (e.g. sterile product manufacture, microbiological issues).
Over recent years, we have had many successes working extensively in the Middle and Far East in developing manufacturers of API and pharmaceutical products according to the relevant requirements, including site preparation for regulatory inspections and support during the inspection.
Sanbec Consulting (SC) has wide experience of auditing and training in the pharmaceutical industry, gained by working in major pharmaceutical companies for over 30 years.
With our associates, we are able to offer experience and expertise of more than 100 years in the pharmaceutical industry. Having worked at director level all staff are professionally qualified and currently belong to several working committees relating to GMP, GDP, Parenteral drugs and Excipients.
Our clients include regulatory agencies, many global pharmaceutical companies and suppliers to the industry (both large and small), with contracts lasting from a few days to six months in duration.
SC can provide support in many areas and are able to call on their specialist associates as required (e.g. sterile product manufacture, microbiological issues).
Over recent years, we have had many successes working extensively in the Middle and Far East in developing manufacturers of API and pharmaceutical products according to the relevant requirements, including site preparation for regulatory inspections and support during the inspection.