Brian has over 25 years experience in industry, including over 12 years in senior management training roles for multinationals such as Pfizer and Abbott Laboratories in the UK.

In these roles, Brian was part of the corporate education and training initiatives for employee development and global performance management programs. 

Brian specialises in professional learning and development initiatives and compliance training.

More recently, Brian has developed the concept of Behavioural GMPs™, a leading edge initiative to change compliance culture within the regulated life sciences industry.

Steve Williams
Director

Steve has over 35 years experience in the life sciences industry in quality assurance, manufacturing and consulting. 

He has developed and delivered multiple training courses for GMP, GLP, risk management, validation, HACCP, and medical devices in Australia and Asia. 

Steve regularly presents at conferences and industry seminars on a range of subjects relating to QA, QMS, risk management, and GMP compliance. He also specialises in blended and e-learning compliance training solutions.

Steve is currently Chairman of the ISPE CPIP Commission for certifying industry professionals.   

Tony Rowland
GxP Director

Tony has over 40 years in industry, specialising in GMP compliance to FDA, TGA and PIC/s codes of GMP.

Tony has successfully conducted many GMP upgrade programs across the Asia Pacific region, project managed validation and licensing of GMP facilities, and is a registered WHO and Veterinary Medicines (APVMA) auditor.

Tony is a regular industry speaker and industry trainer in GMPs and Quality Assurance in the region, and has designed and implemented national public GMP training programs in Australia, Singapore and Malaysia.

Louise White
Education Director, Senior Consultant

Louise has over 28 years experience in the pharmaceutical industry. As Education Director for SeerPharma, Louise is responsible for the design, development and delivery of GxP-related programs across the region.

As a senior GMP consultant, Louise has worked with biopharmaceutical organisations to design and implement quality management systems to both FDA and European cGMP standards.

Louise is a registered  GMP auditor for the APVMA.

Kerry Turner
Senior Consultant

Kerry has almost 20 years experience in the pharmaceutical industry in quality control, quality assurance, R&D, regulatory, packaging and systems. Kerry has implemented quality systems, improved processes through OEE, Kepner Tregoe and Six Sigma methodologies, project managed transfers, product launches and system implementations, written investigation guidelines and training manuals.

Kerry has experience in Australia, UK and the USA.

Kerry's areas of expertise include continuous improvement, quality systems, QA and QC, GxP training, RFT, FDA/TGA and MHRA cGMP compliance, and gap analysis FMEA and HACCP.