For course details click on the subject areas shown in menu below. To contact us: +44 1635 866699 [email protected]

The Team at Inspired Pharma

Short Bio's of the people involved delivering our training courses and consultancy services
Dominic Parry

Dominic Parry

Dominic Parry has worked in the pharmaceutical industry since 1992 and is a leading pharmaceutical quality management specialist. He worked for 4 years at Evans Medical Limited (now Novartis Vaccines) as a Production Development Scientist. He then moved to Hoechst Marion Roussel (now Patheon, UK), where he worked for 4 years as a Quality Assurance Officer and then Validation Manager for the sterile manufacturing operations.

Over the past 15 years, he has worked as a leading pharmaceutical GMP trainer and Quality Management System specialist. He works closely with pharmaceutical companies and their suppliers on evaluating, developing and continually improving their quality systems.

He is generally recognised as one of the leading GMP trainers in the UK and brings an enormous amount of interest, enthusiasm and fun into the training he presents. He is Managing Director of Inspired Pharma Training Ltd.

Peter Lavis

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.

Matt Morris

Matt Morris

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.

Vanessa Parry

Vanessa started her career in the pharmaceutical industry working for Celltech (now Lonza) in 1989 primarily working in their manufacturing sites, as a cell culture and fermentation technician.   After moving to Evans Medical Limited (now Novartis Vaccines), Vanessa worked in Quality Assurance and then specialised in Documentation.  Vanessa then worked for Oxoid (now Thermo Fisher Scientific Oxoid Ltd) for 3 years also in Quality Assurance where she trained as an internal auditor.  Following this, Vanessa became a Customer Operations Consultant for GlaxoSmithKline providing first line support during and after their SAP implementation specialising in production and manufacturing areas. 

Andy Martin

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.

Christine Morris

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.

Robert Smith

Robert is a qualified pharmacist, Qualified Person and Vice-Chair of the Royal Pharmaceutical Society QP Eligibility Panel of Assessors.  He has spent over 25 years working in the pharmaceutical industry.  During his career he has spent time working in both clinical trial supplies and the commercial sector of the pharmaceutical industry.  He is currently a pharmaceutical consultant and has been since leaving his role as Global Head of Quality for the Clinical Pharmacy Research Services at Genzyme, in 2012.   He is a committee member of the Clinical Supplies Discussion Group

Mark Powell

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 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

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 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 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 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.

Dr Douglas Thorogood

Dr Douglas Thorogood is a Quality Assurance and Sterility Assurance Expert. His former roles include senior management positions in Production, QC and QA, Regulatory Affairs and Research Development for Baxter Healthcare located in U.K., U.S.A. and Belgium. His experience also includes the use and application of isolator technology and development of Aseptic Processes. Douglas’ qualifications include a Bachelor of Medicine and Surgery, from Guys Hospital London University and a Doctor of Philosophy.

Does your organisational culture “get” data integrity and it’s importance?

 The MHRA’s GXP data integrity guide was published in March 2018. ‘GXP’ refers to the various good practices regulated by the UK MHRA, including the Good Laboratory Practice Monitoring Authority...

The Golden Rules of GMP – a free GMP video

This free GMP video lasts less than 2 minutes and you can download it for your personal use OR as a part of any refresher/compliance training programme you are running in your organisation providing you leave the opening and closing credits part of the video.

Guidance for starting a new QMS for a Pharma organisation

This article offers detailed advice for those people working in the Pharma secor who are facing the daunting task of starting a new QMS for the first time.

Pharma supplier selection, approval and management

In this article we explore the controls needed to both approve Pharma suppliers and to control the purchasing of materials from them

The 2018 MHRA GDP Symposium

For those of you who did not attend the 2018 MHRA GDP Symposium or missed their recent blog the key highlights are in this article

GMP Quality Metrics – moving beyond traditional measures

This article/video features in our final main unit of our online QMS courses and concerns itself with improving our Quality Management System. In order to improve our system we need to monitor and...

Online GMP and GDP courses approved by the Royal Society of Chemistry

We are very pleased to announce that the Royal Society of Chemistry has just approved our suite of online Pharma compliance/refresher training courses

The roles of the Heads of Production & QC and the Qualified Person

In this video, we look at “The roles of the Heads of Production & QC and the Qualified Person” and what GMP’s requirements are when it comes to roles and responsibilities as well as the specific duties of these three individuals.

Pharma News and Articles

Read our articles on  Pharma regulatory developments as well as news about our Pharma training courses.

About Inspired Pharma

We help people in Pharma organisations to continually improve their regulatory systems to gain competitive advantage and ensure compliance.

We offer a wide range of highly praised and respected classroom and online training courses and also provide our global pharma clients with consultancy support. Our classroom courses are available on a public schedule and also can be customised for inhouse delivery at a client site.

Quick Links

Find your way quickly to any  part of our website by selecting any of the links in this section

Forthcoming Public Courses

2020

January

20 Pharma GMP Lead Auditor

28 Responsible Person

February

Data Integrity

11 Good Manufacturing Practice

25 Documentation & Records

March

2 Pharma GMP Lead Auditor Japan

16 Pharma GMP Lead Auditor

24 Advanced Good Manufacturing Practice

31 Good Distibution Practice

31 Sterile Products

All pharma training courses held in Reading UK unless stated otherwise. Click on course name for full details.

For more 2020 dates select the green 'See all Courses and Dates' button.

Online courses available anytime anywhere

Data Integrity

Good Distribution Practice (GDP)

Good Manufacturing Practice (GMP)

Pharma Quality Management Systems module

QP Medicinal Chemistry & Therapeutics module

QP Quality Management Systems module

Each course typically consists of 10-20 minute chapters of content followed by a quiz based assessment. The QP courses feature tutor assessment too. The learning is accessed over the internet using desktop computers, laptops, tablets and even smartphones.

Why not subcsribe to our mailing list to try a free Taster  of these courses to see if they are of interest?

Visit our Independent Reviews.io website