Peter Lavis

Peter is arguably the finest Quality Management Systems tutor in the business, his enthusiasm for quality system thinking and his outstanding training abilities have gained him international praise and appeal.  He is an IRCA registered Quality Management Systems Lead Auditor.  Peter is an enthusiastic trainer with over 30 years of quality and industrial experience, including spending the past 15 years working closely with pharmaceutical organisations small and large.

Christine Morris

Christine started her career with Sanofi Winthrop working in QC over 20 year’s ago, moving through to the QA Department and from there into QP training as her career progressed, finally working as Head of Quality.  She has extensive experience of working in both ethical and generic pharmaceutical companies and with a wide range of dosage forms.  She is eligible to work both as a Qualified Person (QP) and a Responsible Person (RP), having extensive GMP and GDP experience internationally.

Matt Morris

Acknowledged and admired as a highly focused and committed consultant and coach, Matt is a dynamic, energetic and authentic trainer who demonstrates his passion and communicates this to all who encounter him. He began his Pharma career at Napp Laboratories before having short spells in related industries. He then spent 15 years with GlaxoSmithKline gaining extensive knowledge of GMP from roles in Packaging, Logistics and QC.

His in-depth knowledge of the requirements of Secondary Manufacturing and Packaging have been gained from close collaboration with QPs and other Quality functions whilst managing investigations into Quality Incidents.

More recently, Matt worked as GMP Learning and Development Manager for Lonza Biologics and draws on all his varied experience to create a lively, relevant training environment.

Matt has trained and coached at all levels within organisations and has a genuine passion for people and their development.

Andy Martin

Andy started working in the Pharmaceutical industry in 1985 as a lab technician for Smith & Nephew.  Following this he had a number of roles culminating when he took over as QA Microbiology Manager.   In 2003 he moved into Pharmaceutical Training and then in 2007 he moved back into Microbiology when he took up the position of Microbiology Manager for Catalent Pharma Solutions.  Since 2012 he has operated as a consultant specialising in Microbiology and Quality Systems.

Mark Powell

Mark is a Fellow of the Royal Society of Chemistry with over 25 years’ experience as an analytical chemist. He is an expert in chromatography, spectroscopy and pharmaceutical dissolution testing.  Until September 2013, he was Scientific Manager at Quay Pharmaceuticals, a contract research and manufacturing organisation, where he was responsible for analytical development and technical training.  He now works as a trainer and consultant specialising in laboratory quality systems, chemical analysis and technical writing.

David Thompson

David is a Computer Systems Validation and Compliance expert. He has worked in the IT/Computer Systems arena for almost 30 years, the last 16 years he has provided Consultancy, Auditing and Training to the pharmaceutical/biotech and healthcare industry across the UK, Europe, Asia and the U.S.A. He is a Chartered Engineer with both the MIET and the MInstMC and a member of the GAMP MES SIG. He is involved in our data integrity and computers systems auditing courses.

Martin Lale

Martin Lale has worked in the pharmaceutical and packaging industries since 1978.  He initially worked at Wellcome for 10 years within Packaging Development, before moving to Bristol Myers Squibb to become the Nightshift Operations Manager for a further 4 years.  In addition, he has also worked for Mallinckrodt Animal Health, Eli Lilly and GSK in a variety of supply chain and leadership roles over 20 years.  In the last few years, he has worked on implementing new quality systems and helping suppliers improve their performance.

Ray Munden

Ray has over 35 years of experience working in Pharmaceutical Development in a range of scientific and managerial roles. During this period he has been actively involved in product development, stability testing, stability sample and facilities management, mainly for GlaxoSmithKline. He has a particular expertise in stability testing, for which he has run numerous training courses, and is an acknowledged expert in the efficient design of stability protocols.

MIke Breese

Mike has over 35 years of successful and varied experience in the Pharmaceutical Industry. During that time he undertook a range of scientific as well as managerial roles for multi-national companies in Research & Development, Clinical Trials, Manufacturing and Quality Assurance. He has also travelled extensively throughout the world playing a critical role in the setting up and development of major manufacturing facilities and sites. In his current role he provides services as a contract Qualified Person and pharmaceutical consultant

Ron Orme

Ron has been involved in the learning and development industry for over 20 years. He is a Fellow of the Learning and Performance Institute and in 2004 received the LPI ‘Colin Corder’ award for outstanding services to the training industry. He is the architect behind our website and our learning platform and also develops the web-based learning courses that we now offer to support many of our learning programmes. In addition, he also provides general business support on strategy and sales and marketing.