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An Introduction to Pharmaceutical Packaging Training Course

This course provides an essential overview of pharmaceutical packaging and will be valuable for newcomers to this field. It will also act as a good refresher for those with more experience.

28-29 Mar 2022

& 13-14 Jun 2022 , 28-29 Sep 2022

Book now

Details

Course overview

Pharmaceutical packaging is a very specialised area with its own unique issues and challenges. This introductory course will provide delegates with a good basic grounding and appreciation of what is required for the packaging of pharmaceutical and healthcare products.

A regulatory overview will be given by an expert in the field to ensure that all participants are fully aware of the requirements. The programme will then address the choice of packaging and discuss compatibility, ICH testing, extractables and leachables. There will be detailed coverage of the role of packaging in new product development, together with the main pharmaceutical packaging formats and materials available. Sessions on trade and transit requirements, environment, artwork, and more specific areas such as child-resistant closures and tamper-evident packaging will complete the course and ensure that all delegates leave with a comprehensive understanding of all key aspects of this topic.

Benefits of attending:

  • Gain a useful insight into packaging component and material selection
  • Learn key properties of various packaging materials/systems
  • Appreciate pack testing and evaluation
  • Better understand packaging component specifications
  • Hear about printing processes and controls
  • Acquire knowledge on artwork generation and control
  • Ensure that you comply with the regulatory requirements
  • Learn about transit packaging
  • Consider trade/supply chain requirements

Who should attend?

Whether you are new to the industry, have a basic understanding of pharmaceutical packaging or are more familiar with the area but looking for a refresher, this course will provide you with valuable knowledge and insights from an expert who has worked in the field for more than 25 years.

Those who would benefit from attending include:

  • Account managers
  • Artwork producers
  • Auditors
  • Business developers
  • Clinical trial suppliers
  • Logistics personnel
  • Packaging design/labelling personnel
  • Project managers
  • Purchasers
  • Quality assurance and control personnel
  • Regulatory personnel
  • Suppliers to the industry
  • Technical writers

Programme

The role of pharmaceutical packaging

Special aspects of pharmaceutical packaging

Regulatory and GMP Requirements

  • Agencies, guidelines and legislation
  • Dossier requirements
  • International Conference on Harmonisation (ICH)
  • Common Technical Document (CTD)
  • Summary of Product Characteristics (SmPC)
  • Differences between submissions in the EU and USA
    • Bar coding (briefly) – EAN, 2D – datamatrix, QR
    • Counterfeiting and product security
    • Drug Quality and Security Act
    • Falsified Medicines Directive (FMD)

Choice of pharmaceutical packaging

  • Compatibility and ICH testing
  • Testing and evaluation
    • Extractables and leachables

New product development (NPD) process and role of packaging

Main pharmaceutical packaging formats and materials

  • Primary – key properties – glass, plastics, metals, blisters, laminates, tubes, aerosols, closures
  • Secondary – pharmaceutical labelling – labels, leaflets (PILs), cartons
  • Manufacture, benefits, potential Issues, testing

Trade / transit requirements

Specifications

Environment

Some special requirements for packaging

  • Medical devices – (briefly) – Categories, CE marking requirements
  • Child resistant closures
  • Tamper evidence
  • Readability
  • Braille
  • Patient compliance

Key takeaway messages

Presenter

Chris Penfold (More...)

Experienced Freelance Packaging Development Specialist and Consultant. Chris Penfold is a self-motivated, achievement oriented, confident and creative leader with a proven track record in general and technical management. He is a packaging professional with over 25 years packaging development and NPD experience working on £million-brands in the OTC, healthcare and Rx pharma arenas for ‘blue-chip’ multinational companies such as Glaxo (GSK), CIBA (Novartis), Boots Healthcare and Reckitt Benckiser Healthcare.

He is an MBA graduate and Chartered Marketer with extensive cross-functional experience in a broad spectrum of related disciplines, including marketing, supply chain, QC and production. An ‘International Player’ with experience working in various European countries, Middle East, North America and extended business trips to the Far East. Underpinned by proven interpersonal skills, the ability to make things happen and experience gained from independent international consultancy projects and running his own business, Design Cognition Ltd.

Specialities and Competencies:

Chris’ technical competence and commercial foresight underpin his expertise in design strategy and management. He has many years experience in New Product Development, management and delivery and has pioneered outsourcing opportunities by developing processes, best practice and new ways of working to deliver top and bottom line business benefits – predominantly in the healthcare industry. This has included benefits through his large and reliable network of Far Eastern product and tooling sourcing, development and supply partners.

Chris’ extensive knowledge of all packaging principles and processes includes: plastics and plastic conversion processes, glass, laminates, paper/board together with knowledge of printing technology, reprographics and origination principles. He has an in-depth knowledge of healthcare legislation, including working at the ‘cutting edge’ of Braille implementation.

Book now

Book now

28-29 Mar 2022
Live webinar
28-29 Mar 2022
Live webinar
GBP 1,299 1,099
EUR 1,859 1,579
USD 2,098 1,786
Until 21 Feb 22*
Enrol now
to attend
Live webinar
13-14 Jun 2022
Live webinar
13-14 Jun 2022
Live webinar
GBP 1,299 1,099
EUR 1,859 1,579
USD 2,098 1,786
Until 9 May 22*
Enrol now
to attend
Live webinar
28-29 Sep 2022
Live webinar
28-29 Sep 2022
Live webinar
GBP 1,299 1,099
EUR 1,859 1,579
USD 2,098 1,786
Until 24 Aug 22*
Enrol now
to attend
Live webinar

Learn more about our face-to-face and webinar training formats.

* Note the early booking discount cannot be combined with any other offers or promotional code

Continuing professional development

This course qualifies for 12 hours for your CPD records.
More about CPD

Customised in-house training

We can customise this course to meet the requirements of your organisation and deliver it at your location and/or online.

Contact us

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Previous customers include...

  • AbbVie GmbH & Co KG
  • ALIMS (Medicines and Medical Devices Agency of Serbia)
  • Amicus Therapeutics
  • AS Kalceks
  • BIAL - Portela & Ca, S.A.
  • Boehringer Ingelheim Animal Health Denmark A/S
  • DENTSPLY Implants Manufacturing GmbH
  • F. Hoffmann-La Roche Ltd.
  • Galderma SA
  • Gilead Sciences
  • GSK
  • GSK Vaccines
  • Laboratorios Farmaceuticos Rovi
  • LEO Pharma A/S
  • Martindale Pharma
  • Masters Speciality Pharma
  • Norgine
  • Novo Nordisk
  • Portal Instruments
  • Saudi Food and Drug Authority
  • Suerte Pharma Limited
  • Swedish Orphan Biovitrum AB (publ)
  • Tilray Portugal, Unipessoal Lda.
  • Vectura Ltd
  • Vifor Pharma Ltd.
  • Vifor Pharma Management Ltd.

Overall I quite enjoyed the webinar. Everything was thoughtful and easy to perceive. Particularly I liked the part when speaker introduced with the requirements of registration purposes in United States and compared with EU regulations.

Alise Spakevica, AS Kalceks, Sep 21

Chris was friendly, approachable he has a wealth of knowledge and was happy to answer any questions. The course was very informative, its given me an insight into Regulatory overview and New Product developments and requirements of materials. Happy with the file given which can be referred back to if needed.

Lisa Hughes, Data & Artwork Implementation Administrator, Norgine Ltd, Sep 18

I enjoyed this course, I felt it delivered on its content and would recommend to a colleague. I think the speaker was knowledgeable in his field and facilitated open and interesting discussions throughout the course which meant people were comfortable to ask questions...

Becky Greenan, Senior Manager , Vectura Ltd, Sep 18

All compliments. The course was very interesting and covered a lot of topics in this area.

Milan Milojevic, Associate in Licensing Department for Human Medicines, ALIMS (Medicines and Medical Devices Agency of Serbia), Apr 18

Everything was excellent.

Iva Kapetanovic, Associate in Quality Management Department , ALIMS (Medicines and Medical Devices Agency of Serbia), Apr 18

Good informative slides covering the whole process.

Leah Frederiksen, Regulatory Affairs Compliance Officer, Martindale Pharma, Apr 18