Presented by
Management Forum
This course has been designed to present a number of important developments in pharmaceutical packaging and labelling from regulations, standardisation and technology to innovation and artwork origination.
14-15 Dec 2021 + 2 more dates
This seminar has been designed to present a number of important developments in pharmaceutical packaging and labelling regulations, standardisation, technology, innovation and artwork origination. The importance of packaging and labelling trends to improve patient safety and compliance and increase efficiency will be a particular focus of this event. New technologies and packaging innovations will be discussed and examples and case studies will be illustrated.
Benefits in Attending:
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
George Barrie is a Consultant to the Pharmaceutical Packaging Industry.
Until recently he was with Actavis where his role was to bring all elements of packaging design, regulatory requirements and production together and explore design-led solutions, thus aiding compliance and embracing forward-thinking across the packaging process and value chain. He headed up a team that provided a centralised ‘Packaging Centre of Excellent’ supplying Actavis operations globally. The team was and continues to be, driven by the philosophy of “Making Medicine Accessible”.
He started out with a background in design and subsequently moved into the print and packaging field 12 years ago where he gained broad experience working for a supplier to innovator pharmaceutical companies. Experience on both sides of the packaging value-chain has given him a unique insight into some of the key problems and solutions facing the Pharmaceutical sector.
He is an active member of a number of Pharmaceutical industry bodies and firmly believes that successful packaging design and development will be best achieved by a fully consultative process.
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
IRCA Certified QMS & PS 9000 Lead Auditor.
After working for over 30 years in the pharmaceutical industry, Tony Harper provides auditing, consultancy, training and certification services for the Pharmaceutical and Medical Device Industries and their suppliers particularly those implementing ISO 9000, ISO 13485, ISO 15378, PS 9000 and PS 9100. He also carries out Notified Body CE Medical Device audits.
He was instrumental in setting up the Institute of Quality Assurance (IQA), Pharmaceutical Quality Group (PQG) in 1977 and was its Chairman for 15 years. He was a Committee Member until 2005 and is currently a member of the PQG Partners Team who have developed the PS 9000 Series of documents. He is also a Trustee, Board Member and Honorary Treasurer of the Chartered Quality Institute (CQI). In addition, Tony lectures on Quality Management at the Brighton University QP Post-Graduate Diploma course.
As the UK principal expert, he is working with the International Standards Organization drafting standards (ISO 9001, ISO 9004) and ISO 15378 for Pharmaceutical Packaging Materials and with BSI, CEN and ISO on Braille, patient information and tamper evidence. He is Chairman of the Braille Medicines Forum. Tony is also working on pharmaceutical artwork/origination guidelines.
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
Suzanne Ivory joined the Perigord Group in 2005 where she currently works as the Group Quality Manager for the software development, artwork management and printing sections of the business.
She has 18 years experience as a Quality Manager implementing and managing quality systems such as ISO 9001:2008 and PS 9000 in a range of companies which service the pharmaceutical industry including Printing, Finishing, Packaging, Artwork studio’s and Software development. Suzanne is a qualified IRCA auditor for ISO 9001: 2000, ISO 14000 and PS 9000.
Over the last 3 years she was heavily involved in updating the PS9000:2011 standard which was published on the 14th September 2011. This involved working with a team of industry experts from pharmaceutical companies and suppliers to the pharmaceutical industry giving her a detailed insight into the audit requirement and best practises within the pharmaceutical packaging environment.
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
Jan MacDonald is a pharmacist by profession and is currently Group Manager for the Access, Information and Medicines Standards Group in the Vigilance and Risk Management of Medicines Division at the MHRA. She has undertaken a number of assessment and management roles within the agency. Prior to this she was principal pharmacist for quality assurance and quality control in the NHS.
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
Edelmann GmbH, Heidenheim/Germany
Dieter Mößner has been working as Project Engineer Pharma and was previously a team leader in the Prepress area for Edelmann GmbH. He has been responsible for artwork services and for print data communication for the Edelmann group (www.edelmann.de) producing folding cartons, leaflets and labels for the pharmaceutical and cosmetics industries in 13 sites world-wide. His job is to consult customers and artwork agencies in artwork creation, print data communication and typesetting workflows.
He composed parts of the “Technical Guidelines Braille on folding cartons”, published by the German Folding Cartons Association FFI (www.ffi.de), and the guidelines “Braille on Folding Cartons”, published by the European Carton Makers Association ECMA (www.ecma.org). He is Convenor of CEN/TC 261/SC 5/WG 12 “Marking”. This working group at the European committee for standardisation CEN (www.cen.eu) has created the European standard EN 15823:2010 “Braille on Packaging for Medicinal Products”. It has just recently completed the works on the creation on EN 16679 – the European standard on “Tamper verification features for medicinal product packaging”. Up to its publication in January 2013 the contents of the European standard EN 15823 had been transformed into an International standard ISO 17351 “Braille on packaging for medicinal products” within ISO/TC 122 packaging. This project has been processed within ISO/ TC 122/WG 9 “Accessible design” with Dieter Mößner / Germany as project leader.
He is also Chairman of the German working groups NA 115-03-01 AA “Braille on packaging” and “Tamper verification features for medicinal product packaging”. After six years being the Vice-chairman of the packaging standards committee NAVp (www.din.navp.de) at the German Standards Institute DIN (www.din.de) he became its Chairman in March 2013.
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
Chris Waterhouse is Managing Director of iDi Pac Ltd, a member of the Packaging Collective Leadership team as well as a former Chairman of the UK Packaging Society.
Chris has over 30 years’ experience in the Packaging Industry having worked in a variety of roles and sectors; Packaging and Supply Chain strategy, machine operation and maintenance as well as Packaging Innovation and Development in Pharma, AgChem, FMCG, cosmetics and drinks.
Acknowledged as an industry “go to” professional providing support, networking and energy into growing capability in packaging.
Chris’s Employment History is as follows: -
iDi Pac Ltd, Petersfield, England 2007 to date
Managing Director
Passionate in “Solving Current and Future Challenges in Packaging and the Supply Chain. Sustainable solutions for today and tomorrow through a highly effective and skilled team.
Syngenta AG, Basel Switzerland 1998 to 2007
Head of Packaging Development
Responsible for technical Development on a $175mio pa technical spend. Consolidation and integration of legacy packaging team’s post-merger of Zeneca and Novartis AgChem businesses.
Global Fill & Pack Strategy Manager
Responsible for development of the Fill & Pack portfolio with innovation projects globally; USA, Brazil, Asia & Africa.
Gulf Oil (GB) Ltd, Silvertown, London England 1992 to 1998
Production Superintendent
Responsible for site operations and capital programme
14-15 Dec 2021
27-28 Jun 2022
12-13 Dec 2022
Nathy Feely, Short Mountain Consulting, is a highly experienced professional in the field of packaging, artwork and organisational design. As an independent consultant he is in an excellent position to assess organisations, advise on strategic options and implement agreed plans. His expertise is in procurement and management of outsourced services, as well as product security and anti-counterfeiting technologies.
Prior to establishing Short Mountain Consulting he was Director, Packaging Services at Wyeth (and after acquisition, Pfizer) where he established EMEA Packaging services, primarily concerned with integrating Packaging and Artwork elements into the greater product Supply field.
14-15 Dec 2021
Live online
09:00-16:45 UK (London) (UTC+00)
10:00-17:45 Paris (UTC+01)
04:00-11:45 New York (UTC-05)
Course code 11915
Until 09 Nov
27-28 Jun 2022
Classroom
London venue TBC
09:00-17:15 UK (London)
Course code 11914
Until 23 May
12-13 Dec 2022
Live online
09:00-17:15 UK (London) (UTC+00)
10:00-18:15 Paris (UTC+01)
04:00-12:15 New York (UTC-05)
Course code 11916
Until 07 Nov
Very good standard of speakers as always.
Oct 23 2019
Cath Norris 
Global Packaging Technologist, Norgine Ltd
Oct 23 2018
Excellent, very informative
Caroline Byrne 
MDM Artwork Assistant, Servier Industries Ireland
Oct 23 2018
Speakers were well prepared.
Zeljka Davosir Klaric 
Coordinator for National Procedure, Croatian Agency for Medicinal Products and Medical Devices
Oct 23 2018
Friendly and well organised.
Andy Linney
Principal Designer , Cambridge Consultants
Oct 10 2017
Professional, detailed and relevant. Up to date and pitched at the right level
Daniel McNaught
Senior Director, EU Manufacturing and Supply Chain, Zogenix International
Oct 10 2017
Really excellent content and speakers
Martina Forristal
Quality Manager, Perigord Premedia Ltd
Oct 10 2017
Content and presentations were very interesting, speakers kept good atmosphere.
Petra Dimić
Artwork and Module 1 Specialist, Xellia d.o.o
Oct 10 2017
Very good effort!
Vasiliki Ntafi 
Global Quality Manager, F. Hoffmann-La Roche Ltd
Oct 10 2017
Experienced speakers providing valuable recommendations. Helpful concrete examples
Peggy Pontabry
Regulatory Labelling Manager, F. Hoffmann-La Roche Ltd
Oct 10 2017
All very informative and well run
Rachel Barclay
Associate Director Labelling & Artwork , Norgine Ltd
Oct 10 2017
I enjoyed the conference - very informative and a good pace. It never felt like it was "dragging on".
Nick Godden
Clinigen Group plc
Oct 11 2016
A very well put together course covering the current labelling challenges facing the pharma industry in meeting the latest regulations. The speakers were all very enthusiastic about sharing their knowledge and giving guidance to improve how we work in this industry. I have been on one of these courses before and think it is essential to attend every few years to keep abreast of the latest topics.
Liz Campbell
Artwork Co-ordinator, Britannia Pharmaceuticals
Oct 11 2016
Overall, I would say the presentation was good and speakers were professional and friendly
Mreena Ballah Pulton
Global Packaging Technologist, Norgine Limited
Oct 11 2016
An excellent course to broaden the mind of packaging-orientated emplyees with presentation from passionate industry-leading key figures giving me confidence that what I was being taught was the best information/opinion available
Adam Goodall
Artwork Specialist, Otsuka Pharmaceuticals Europe Ltd
Oct 11 2016
I did enjoy the course, all speakers were great and kept the momentum going
Shelley Browning
Senior Regulatory Affairs Officer, The Boots Company PLC
Oct 11 2016
Very interesting topics
Thierry Adatte
Associate Manager, Celgene Logistics Sàrl
Oct 11 2016
Course was good and speakers very engaging
Barbara Pisano
Scientific Assessor, MHRA
Oct 11 2016
It was good, very useful and I will recommend it to our staff
Nawaf Matar AlMotairi 
Saudi Food and Drug Authority
Oct 11 2016
I appreciated the limited number of participants, which allowed to have discussions within the group during the sessions as well as exchange of experience with other participants during breaks
Tamara Huber
Senior Manager, CSL Behring AG
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