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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.

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.

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. 

Linda Ambrose

Linda Ambrose

Linda Ambrose has a wealth of experience spanning over 40 years in large, small and multinational organisations across Europe, Asia and the USA, in both the public & private sectors and has operated at Director level in both Quality Assurance and Manufacturing Operations.  Linda is a previous Group Manager of the UK’s Medicines Inspectorate (the MHRA).

With an MBA and postgraduate qualifications in psychology, change management and the Neuroscience of Leadership, Linda has developed a specialist interest in the behavioural and psychological aspects of quality management and regulatory compliance, and operational efficiency. 

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.

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

Sarah Pratt

Sarah is a pharmacist with a masters in drug development.  Her career history includes senior and international roles with Sanofi, AstraZeneca and C-suite, managerial and consultancy roles across a number of smaller international innovator and contract organisations in the UK, France and Belgium.  Sarah’s major areas of expertise lie within the GDP and GMP arena within both pharmaceutical development and within commercial manufacture/supply chain sectors and she has held the position of Responsible Person on European wholesale dealers’ authorisations.  She also runs a masters module at Queen Mary University in London on Regulation within the Pharmaceutical Industry.

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.

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.

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

GMP for Engineers course

Following requests from several of our clients we have just released a new Chapter in our very popular GMP online course range aimed at Engineers.

Travel difficulties – online learning may be the answer

With many organisations banning travel, or individuals simply making a personal choice not to travel, online learning can be a valuable way to keep building the skills and knowledge needed for your continued success. 

Coronavirus – an update about our training course programme

We are hearing from several of our delegates that they cannot attend a forthcoming public course they are booked on because of a company travel ban . Also, some people are contacting us to ask if we are still running a course that they are booked on or plan to make a booking on. So, this article is aimed at updating anyone booked on a course or thinking about booking a course on our current approach to this difficult situation.

Our most popular GMP and QMS articles

This article highlights some of our most popular articles

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

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

Virtual Instructor-led courses in July and classroom courses currently scheduled for September

July

7-9 2-3.30pm Good Manufacturing Practice,Virtual Instructor-led 

14 Problem Solving,Virtual Instructor-led 

September

7 Pharma GMP Lead Auditor

15 Documentation and Records

16 Good Distribution Practice

21 Pharma GMP Lead Auditor London, UK 

22 Advanced GMP

October

06 Responsible Person

06  Data Integrity

12 Pharma GMP Lead Auditor Manchester, UK

20 Good Manufacturing Practice

21 Sterile Products

November

10 Internal Auditor

24 Problem Solving

30 Pharma GMP Lead Auditor

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

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.

To try a free taster of these courses to see if they are of interest visit this page.

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