Broughton Director of Product Safety and Compliance, Yvonne Wilding, discusses implications of...
FDA PMTA 90-day deficiency letters – what next?
Broughton Head of Scientific Affairs, Paul Hardman outlines factors that can lead to data gaps in Premarket Tobacco Product Applications (PMTA) and what level of instruction or guidance to expect from FDA.
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Broughton is delighted to announce that Paul Hardman joins as Head of Scientific Affairs. This...
Broughton Chief Regulatory Officer, Dr Nveed Chaudhary shares his thoughts on the latest FDA...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary to present the future challenges of the...
Broughton Chief Regulatory Officer, Dr Nveed Chaudhary announces the launch of our Blue-sky...
Broughton Dr Nveed Chaudhary, Chief Regulatory Officer discusses the EU's stance on Next Generation...
Broughton Dr Nveed Chaudhary, Chief Regulatory Officer, discusses Deficiency Letters and data gap...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary discusses business growth and Broughton’s...
Broughton Regulatory Operations Manager, Emily Saunders, discusses FDAs announcement on the final...
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