Courses

GMP

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

An Introduction to Pharmaceutical Packaging

25-26 Sep 2019

Also on: 17 Mar 2020

A comprehensive review of the regulations and technical requirements for chemistry, manufacturing and control (CMC) management of your application.

Common Technical Document

4-5 Dec 2019

Also on: 2 Jun 2020

Book by 25 Oct to save
£200 / €280 / $312

The latest technologies in connected medical devices, digital health and mobile apps for the pharmaceutical and medical device industries

Book by 23 Aug to save
£200 / €280 / $312

Data Integrity is a critical issue in document governance. It increasingly becoming a focus for regulatory inspections globally. This course will equip you with knowledge necessary to identify and avoid potential Data Integrity issues before auditors do.

Data Integrity and Document Management

27 Sep 2019

Also on: 5 Mar 2020

Linking the technical requirements of device design and pharmaceutical product development.
Using QbD to deliver drug/device combinations.

Book by 4 Oct to save
£200 / €280 / $312

Key annual conference for Pharmaceutical and Medical Device Professionals in the DPI market.

Dry Powder Inhalers

Bespoke training

We can customise this course to meet your requirements.

The ‘how to’ of technology transfer across the product lifecycle

New for 2019

Effective Technology Transfer

19-20 Nov 2019

Also on: 21 Apr 2020

Book by 4 Oct to save
£200 / €280 / $312

An essential course for ensuring compliance with Regulatory Requirements which will be of particular relevance for Pharmacovigilance, Regulatory Affairs, Clinical Research/Operations, GMP, QA and Document Management Functions

How to Write Effective SOPs

2 Dec 2019

Also on: 25 Jun 2020

Book by 24 Oct to save
£100 / €140 / $156

This meeting will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement and CAPA and planning and implementation in practice of improvements and CAPA

Book by 24 Oct to save
£100 / €140 / $156

An essential annual update for inhalation professionals. Industry case studies, regulatory updates, latest therapies and technology innovations.

Inhaled Drug Delivery

6-7 Nov 2019

Book by 23 Aug to save
£200 / €280 / $312

Advances in technology for pens, auto-injectors, large volume pumps, patch pumps, needle-free, pre-filled syringes and other parenteral methods.

Injectable Drug Delivery

18-19 Mar 2020

A comprehensive overview of MDIs including development, manufacture, regulation and market potential

Metered Dose Inhaler (MDI) Technology

18-19 Sep 2019

Also on: 19 Feb 2020

This conference gives a comprehensive review within the field of nasal drug delivery while reviewing the very latest new data and innovative technologies.

Nasal Drug Delivery

14-15 May 2020

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Pharmaceutical Development of ATMPs

7-8 Oct 2019

Also on: 30 Mar 2020

Book by 23 Aug to save
£200 / €280 / $312

This course has been designed to present a number of important developments in pharmaceutical packaging and labelling from regulations, standardisation, technology, innovation and artwork origination.

Book by 6 Sep to save
£200 / €280 / $312

Topics such as quality of syringe manufacture, quality of syringe components and why, quality of filling (volume check, reject reduction), quality of inspection and product release will be discussed in detail.

Pre-Filled Syringes

24-25 Mar 2020

Gain a comprehensive understanding of the EU and FDA Process Validation Guidance, how to establish a Process Validation Programme, understand the link between quality by design and process validation, apply relevant tools for process validation including risk assessment

Process Validation with Qualification

16-17 Oct 2019

Also on: 3 Mar 2020

Book by 6 Sep to save
£200 / €280 / $312

Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learning how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.

Book by 25 Oct to save
£200 / €280 / $312