How to Use Intelligence to Win the cGMP Race
Share This webinar:
Even when Quality, Manufacturing, and R&D professionals try to stay current with regulations and new technologies, they don’t employ a systematic approach. Besides the lost time, they find it challenging to get their voices heard by upper management since there isn’t a process that constantly feeds to management with up-to-date intelligence that has a clear business value.
Because of those challenges, most pharma companies can’t keep up and have turned reactive rather than proactive in facing regulatory changes. Such a reactive and unsystematic approach is then causing risks regarding regulation and standard compliance.
In this webinar, you will gain a good understanding and guidance on creating a systematic intelligence and research process into the ever-changing cGMP, with as little cost and effort as possible. You will learn about various tools to do that- from the most simple and quick solutions to advanced strategies.
After the webinar, you will have less stress fearing losing the cGMP race. You will also feel confident to make a more substantial impact on upper management and drive change based upon facts and intelligence.
Who Should Attend:
Anyone working in the Quality Assurance (QA), Regulatory Affairs (RA) and R&D departments within the following industries:
- Medical devices
- Skill Level: Novice, Intermediate
Nik WellsManaging Director Regulatory Index and IPC
Experienced regulatory expert within the biopharmaceutical industry, with a specialism in insights and intelligence. Over the last 20+ years, Nik has been supporting companies such as Pfizer, Abbott, Mylan and Novartis, assisting with the enhancement of processes and change to support regulatory and quality function within product development.