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.
22-23 Sep 2020
Also on: 17 Mar 2021
A comprehensive review of the regulations and technical requirements for chemistry, manufacturing and control (CMC) management of your application.
1-2 Dec 2020
Also on: 2 Jun 2021
Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.
5 Oct 2020
Also on: 5 Mar 2021
Linking the technical requirements of device design and pharmaceutical product development.
Using QbD to deliver drug/device combinations.
17-18 Nov 2020
Also on: 5 May 2021
A comprehensive overview of DPIs including market trends, treatments formulation, regulation and device design
FULLY UPDATED PROGRAMME
23-24 Jun 2021
The ‘how to’ of technology transfer across the product lifecycle
1-2 Oct 2020
Also on: 20 Apr 2021
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.
3 Dec 2020
Also on: 28 Jun 2021
This course 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.
4 Dec 2020
Also on: 29 Jun 2021
An essential annual update for inhalation professionals.
3-4 Nov 2020
Advances in technology for pens, auto-injectors, large volume pumps, patch pumps, needle-free, pre-filled syringes and other parenteral methods.
10-11 Mar 2021
A comprehensive overview of MDIs including development, manufacture, regulation and market potential
16-17 Sep 2020
Also on: 16 Feb 2021
A comprehensive review of the latest scientific developments, technology advances and regulatory guidance in the field of nasal drug delivery.
15-16 Apr 2021
This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.
5-6 Oct 2020
Also on: 22 Mar 2021
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.
28-29 Oct 2020
Also on: 27 Oct 2021
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.
23-24 Mar 2021
Gain a comprehensive understanding of the EU and FDA process validation guidance, learn how to establish a process validation programme, understand the link between QbD and process validation, apply relevant tools for process validation including risk assessment.
22-23 Sep 2020
Also on: 2 Mar 2021
Design efficient stability studies that are suitable for global marketing. Be able to carry out appropriate stability studies and manage stability samples and facilities, learn how to save resources on stability testing and improve the likelihood of regulatory approval of stability protocols.
2-3 Dec 2020
Also on: 6 Jul 2021