The MHRA’s GMDP Symposium goes Virtual and Real Regulatory will be in Attendance
It’s that time of the year once again! The ‘Good Manufacturing and Distribution Practice’ (GMDP) Symposium will be returning this year in a new virtual format.
This event will bring together wholesalers, quality personnel and pharmaceutical professionals to discuss the latest information and guidance on changing legislation and increasing complexity in the manufacturing and distribution chain.
Our Real expert, Niamh Miller, will be attending and would love to chat to you about compliance issues that could affect your organisation and how our team can produce bespoke strategies no matter what phase of development, ensuring swift and timely approvals.
We look forward to seeing you there! To arrange a meeting at a time convenient to you, contact us today.
Niamh joined the company in June 2016 having spent 15 years working in quality compliance in the medical device sector initially as a QC Supervisor(2 years) before being promoted to QC Manager. Niamh also worked in the pharmaceutical sector from 1990 -2000 in both R&D (method development) and as a QC Chemist in a bulk pharmaceutical manufacturer.
Niamh’s current role in the company is as Regulatory Affairs Consultant.