Quality by Design in Pharmaceutical Development

We are delighted to offer this NEW course now ON LINE, 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, November 9th | 1.30pm – 5.30pm, GMT
Tuesday, November 10th | 1.30pm – 5.30pm, GMT
Wednesday, November 11th | 1.30pm – 5.30pm, GMT
Thursday November 12th | 1.30pm – 5.30pm, GMT
Friday November 13th | 1.30pm – 5.30pm, GMT

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.

Please do view the brochure for more information (please note this is based on the live 3 day course, but the content is the same)

Others Details

Time: 1:30 pm - 5:30 pm Brochure https://go.evvnt.com/626597-2?pid=6581 Artists / Speakers: Dr Paul Murray