Quality by Design in Pharmaceutical Development

We are delighted to offer this QbD course online, this three day course will be divided up over 5 sessions and brought to you via an Virtual Platform, the dates and times are as follows:

Monday, June 3rd | 1.30 - 5.30pm BST
Tuesday, June 4th | 1.30 - 5.30pm BST
Wednesday, June 5th | 1.30 - 5.30pm BST
Thursday, June 6th | 1.30 - 5.30pm BST
Friday, June 7th | 1.30 - 5.30pm BST

QbD is an industry initiative supported by regulators. However, it is also a systematic method of process development which delivers consistency, robustness and increased process knowledge.

This course introduces QbD across all areas of pharmaceutical development including synthesis, formulation and analysis, and suggests practical recommendations for the implementation of QbD.

Participants will learn how to identify and prioritise process parameters, determine and manage risk, and implement control strategies. The use of experimental design (DoE) in QbD, the identification of potential mixing and scale-up problems, and the safe scale up of processes to pilot and manufacturing plants will also be discussed.

For the benefit of process scientists, engineers, formulators, analytical chemists and manufacturing personnel, this course includes highly interactive, hands-on workshops, based on several case studies.

URLs:
Tickets: https://go.evvnt.com/2437048-0?pid=10018
Website: https://go.evvnt.com/2437048-3?pid=10018

Prices:
General Admission: GBP 2099.00,
Printed manual: GBP 120.00

Speaker: Dr Paul Murray