Broughton celebrates Premarket Tobacco Product Application (PMTA) success for clients.
Broughton's Chief Scientific and Regulatory Officer Dr. Nveed Chaudhary talks to leading sector publication Tobacco Asia about ...
Broughton's Chief Scientific and Regulatory Officer, Dr Nveed Chaudhary has published an article on the recent FDA announcement on ...
Broughton's Chief Commercial Officer, Andy Mooney, discusses the latest synthetic nicotine legislation and what this means for ENDS ...
Broughton's Chief Scientific and Regulatory Officer, Dr Nveed Chaudhary discusses what developments are expected over the next 12 months ...
Broughton's Head of Regulatory Affairs, Lloyd Smart discusses Food and Drug Administration (FDA) final ruling for Premarket Tobacco Product ...
Broughton's Chief Regulatory Officer, Dr Nveed Chaudhary shares his post-event reflections on Global Tobacco Nicotine Forum (GTNF) 2021.
Broughton Head of Scientific Affairs, Paul Hardman has recently published an article with leading sector publication Tobacco Reporter.
Broughton Chief Scientific Officer, Chris Allen shares his thoughts ahead of this year's Global Tobacco & Nicotine Forum (GTNF) taking ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary shares his thoughts on yesterday's announcement from the Food and Drug ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary shares his thoughts on the latest Food and Drug Administration (FDA) updates ...
Broughton asked industry expert, Dr Ian Fearon, to explain the process followed when running clinical trials.
Broughton Head of Scientific Affairs, Paul Hardman has today published an article with leading sector publication Tobacco Reporter that ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary, discusses the global challenges the ENDS industry faces to achieve a smoke-free ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary, summarises the latest US Food and Drug Administration (FDA) Centre for Tobacco ...
Broughton Head of Scientific Affairs, Paul Hardman outlines factors that can lead to data gaps in Premarket Tobacco Product Applications ...
Broughton is delighted to announce that Paul Hardman joins as Head of Scientific Affairs. This latest appointment further bolsters the ...
Broughton Chief Regulatory Officer, Dr Nveed Chaudhary shares his thoughts on the latest FDA announcement, ‘Clarification on General ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary to present the future challenges of the ENDS regulatory battleground and the ...
Broughton Dr Nveed Chaudhary, Chief Regulatory Officer, discusses Deficiency Letters and data gap fulfillment and why the time to act is ...
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary discusses business growth and Broughton’s plans to extend its service portfolio ...
Broughton Regulatory Operations Manager, Emily Saunders, discusses FDAs announcement on the final ruling for PMTA applications.
Broughton Director of Product Safety and Compliance, Yvonne Wilding, discusses a leading-edge software tool designed and in use at ...
Broughton Chief Scientific Officer, Chris Allen, discusses the sensitivity of analytical methods appropriate for Toxicological assessment ...
Broughton, Director of Product Safety and Compliance, Yvonne Wilding and Principal Scientist, Louise Neilson will be in attendance and ...
Broughton Director of Product Safety and Compliance, Yvonne Wilding, looks at the recent Tobacco Product Perception and Intention studies ...
Broughton , Director of Product Safety and Compliance, Yvonne Wilding has recently published an article with leading sector publication ...
Broughton announce, Chief Scientific Officer to join panel discussion at GTNF 2020
As the September 9th, 2020 PMTA deadline rapidly approaches, our Chief Scientific Officer, Chris Allen, takes a look at the current US ...
Broughton, Chief Scientific Officer has recently published an article with leading sector publication Tobacco Reporter – Counting Down to ...
Broughton, Chief Scientific Officer has recently published an article with leading sector publication Tobacco Reporter – Measuring up
Broughton announce new webinar.
In silico methods for the prediction of toxicity are becoming more widely used in the field of toxicology.
Broughton has produced an infographic to explain the process for toxicology risk assessments for Electronic Nicotine Delivery Systems ...
Broughton, Marketing Manager discusses changing times, virtual events and embracing technology.
This article provides an overview of the different types of toxicological studies typically undertaken, and how they support regulatory ...
Broughton announce expansion of Toxicology team directed by Yvonne Wilding.
Extension of the Premarket Tobacco Product Application (PMTA) deadline, requested by the US Food and Drug Administration (FDA) due to the ...
A recent announcement from The Food and Drug Administration (FDA) on the Premarket Tobacco Authorization (PMTA) final ruling means that the ...
The US Food and Drug Administration (FDA) has requested an extension to the Premarket Tobacco Product Application (PMTA) deadline due to ...
We’re delighted to announce that Broughton has launched an in-house toxicology services division to increase our capacity and introduce ...
Alan Hutchinson, Principal Scientist at Broughton, has recently published an article with Laboratory News; the leading magazine for UK ...
Are you confused by the ENDS flavor debate? Dr. Ian Fearon, Broughton subject matter expert for clinical studies, has recently published an ...
The US Food and Drug Administration (FDA) has published final guidance regarding Enforcement Priorities for Electronic Nicotine Delivery ...
We’re delighted to announce that Broughton has recently launched an in-house service focused on enabling companies in the Electronic ...
We are delighted to announce that Broughton has made a series of major business transactions to meet the demands of our growing portfolio.
The US Food and Drug Administration (FDA) recently published a “Proposed Rule” for the Electronic Nicotine Delivery Systems (ENDS) sector. ...
As we mentioned in our previous article, Final PMTA guidance has arrived – what’s changed?, FDA has modified the list of constituents or ...
The latest statement from FDA Commissioner, Scott Gottlieb, outlines the agency’s actions to ensure sound regulation of tobacco products, ...
Tobacco product manufacturers are required to comply with certain requirements under Section 904(a) of the Federal Food, Drug and Cosmetic ...
We are delighted to officially announce the recent launch of Broughton Limited, a spin-off from the long-established Broughton. The new ...
It appears so, following a series of significant recent FDA announcements regarding Harmful and Potentially Harmful Constituent (HPHC) ...
FDA regulated industries, including the ENDS industry, have few opportunities to engage with the FDA and receive valuable, bespoke product ...
Save the date. Monday 22nd October is looking like a key day for the US ENDS industry.
Electronic cigarettes are battery powered electronic devices that enable delivery of nicotine to a user without the combustion processes of ...
Last week we attended the Vape and the FDA event hosted by the Vapor Technology Association (VTA) in Washington DC. It was great to catch ...
Maintaining regulatory compliance is a key factor in keeping your Electronic Nicotine Delivery System (ENDS) products on the market. A ...
The FDA has issued its latest guidance to the tobacco product industry, including Electronic Nicotine Delivery Systems (ENDS). The guidance ...
On Friday, July 28th, the FDA issued a press release announcing the new plan for tobacco and nicotine regulation. There has been much ...
With confusion and uncertainty on all sides surrounding the FDA regulations, the ENDS industry came together once again for the Vape and ...
A fascinating debate and discussion were order of the day once again at the latest E-Cig Summit. After the success of the UK events this ...
FDA Announced on 3rd May, 2017 that all outstanding compliance deadlines for PMTA have been extended by 3 Months
On May 10th, 2016, FDA issued a final rule extending its tobacco product authority to all tobacco products (except for accessories of ...