Broughton gains new regulatory insight while ...
May 18, 2022
Broughton celebrates Premarket Tobacco Product Application (PMTA) success for clients.
Designing an NGP and Making it Market-Ready
April 11, 2022
Broughton's Chief Scientific and Regulatory Officer Dr. Nveed Chaudhary talks to leading sector publication Tobacco Asia about ...
Broughton explains how the FDA’s new powers to ...
March 29, 2022
Broughton's Chief Scientific and Regulatory Officer, Dr Nveed Chaudhary has published an article on the recent FDA announcement on ...
US Congress set to close the loophole on the use ...
March 14, 2022
Broughton's Chief Commercial Officer, Andy Mooney, discusses the latest synthetic nicotine legislation and what this means for ENDS ...
2022 will define the future of ENDS
February 24, 2022
Broughton's Chief Scientific and Regulatory Officer, Dr Nveed Chaudhary discusses what developments are expected over the next 12 months ...
FDA final rule for PMTA applications
October 28, 2021
Broughton's Head of Regulatory Affairs, Lloyd Smart discusses Food and Drug Administration (FDA) final ruling for Premarket Tobacco Product ...
GTNF 2021 - Industry reflections
October 8, 2021
Broughton's Chief Regulatory Officer, Dr Nveed Chaudhary shares his post-event reflections on Global Tobacco Nicotine Forum (GTNF) 2021.
ENDS companies left in the lurch
September 20, 2021
Broughton Head of Scientific Affairs, Paul Hardman has recently published an article with leading sector publication Tobacco Reporter.
Broughton join world-leading experts at GTNF 2021
September 17, 2021
Broughton Chief Scientific Officer, Chris Allen shares his thoughts ahead of this year's Global Tobacco & Nicotine Forum (GTNF) taking ...
FDA update - disappointing news or an opportunity?
September 10, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary shares his thoughts on yesterday's announcement from the Food and Drug ...
What the latest FDA updates mean for ENDS ...
September 7, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary shares his thoughts on the latest Food and Drug Administration (FDA) updates ...
Clinical trials, timescales, and supplementing ...
August 9, 2021
Broughton asked industry expert, Dr Ian Fearon, to explain the process followed when running clinical trials.
Deficiency letters - common causes and how to ...
August 5, 2021
Broughton Head of Scientific Affairs, Paul Hardman has today published an article with leading sector publication Tobacco Reporter that ...
Achieving a sustainable smoke-free future is the ...
July 27, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary, discusses the global challenges the ENDS industry faces to achieve a smoke-free ...
US Food and Drug Administration (FDA) Centre for ...
June 16, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary, summarises the latest US Food and Drug Administration (FDA) Centre for Tobacco ...
FDA PMTA 90-day deficiency letters – what next?
June 1, 2021
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 ...
FDA - Clarification on General Enforcement ...
April 30, 2021
Broughton Chief Regulatory Officer, Dr Nveed Chaudhary shares his thoughts on the latest FDA announcement, ‘Clarification on General ...
Broughton is delighted to sponsor and present at ...
April 13, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary to present the future challenges of the ENDS regulatory battleground and the ...
90 days and counting - PMTA Deficiency Letter
February 23, 2021
Broughton Dr Nveed Chaudhary, Chief Regulatory Officer, discusses Deficiency Letters and data gap fulfillment and why the time to act is ...
Dr Nveed Chaudhary joins Broughton and discusses ...
February 19, 2021
Broughton Chief Regulatory Officer, Dr. Nveed Chaudhary discusses business growth and Broughton’s plans to extend its service portfolio ...
PMTA - The Final Rule
February 3, 2021
Broughton Regulatory Operations Manager, Emily Saunders, discusses FDAs announcement on the final ruling for PMTA applications.
ToxHQ System For Product Formulation
January 20, 2021
Broughton Director of Product Safety and Compliance, Yvonne Wilding, discusses a leading-edge software tool designed and in use at ...
Sensitivity of analytical methods - LOD/LOQ
December 16, 2020
Broughton Chief Scientific Officer, Chris Allen, discusses the sensitivity of analytical methods appropriate for Toxicological assessment ...
Join us at the American College of Toxicology ...
November 12, 2020
Broughton, Director of Product Safety and Compliance, Yvonne Wilding and Principal Scientist, Louise Neilson will be in attendance and ...
What does the new TPPI guidance mean to ENDS ...
November 6, 2020
Broughton Director of Product Safety and Compliance, Yvonne Wilding, looks at the recent Tobacco Product Perception and Intention studies ...
Post Market Requirements - A journey, not a ...
October 16, 2020
Broughton , Director of Product Safety and Compliance, Yvonne Wilding has recently published an article with leading sector publication ...
Hot Topic - Comparative Regulations, GTNF 2020
September 14, 2020
Broughton announce, Chief Scientific Officer to join panel discussion at GTNF 2020
PMTA - Where next?
September 7, 2020
As the September 9th, 2020 PMTA deadline rapidly approaches, our Chief Scientific Officer, Chris Allen, takes a look at the current US ...
Counting Down to the PMTA deadline.
September 3, 2020
Broughton, Chief Scientific Officer has recently published an article with leading sector publication Tobacco Reporter – Counting Down to ...
Measuring up
August 13, 2020
Broughton, Chief Scientific Officer has recently published an article with leading sector publication Tobacco Reporter – Measuring up
Skin sensitization in silico protocol
July 17, 2020
In silico methods for the prediction of toxicity are becoming more widely used in the field of toxicology.
A Guide To Toxicology Risk Assessments
June 11, 2020
Broughton has produced an infographic to explain the process for toxicology risk assessments for Electronic Nicotine Delivery Systems ...
Virtual reality - time to get creative!
June 5, 2020
Broughton, Marketing Manager discusses changing times, virtual events and embracing technology.
What is Toxicology for ENDS
May 19, 2020
This article provides an overview of the different types of toxicological studies typically undertaken, and how they support regulatory ...
Blog: Expansion of Toxicology team at Broughton
May 1, 2020
Broughton announce expansion of Toxicology team directed by Yvonne Wilding.
Breaking news: PMTA deadline extension agreed
April 22, 2020
Extension of the Premarket Tobacco Product Application (PMTA) deadline, requested by the US Food and Drug Administration (FDA) due to the ...
Update on Premarket Tobacco Product Application ...
April 6, 2020
A recent announcement from The Food and Drug Administration (FDA) on the Premarket Tobacco Authorization (PMTA) final ruling means that the ...
FDA requests PMTA deadline extension
March 31, 2020
The US Food and Drug Administration (FDA) has requested an extension to the Premarket Tobacco Product Application (PMTA) deadline due to ...
Broughton launches toxicology services department ...
March 4, 2020
We’re delighted to announce that Broughton has launched an in-house toxicology services division to increase our capacity and introduce ...
Safeguarding the smoking gun
February 19, 2020
Alan Hutchinson, Principal Scientist at Broughton, has recently published an article with Laboratory News; the leading magazine for UK ...
ENDS manufacturers encouraged to take the lead on ...
January 31, 2020
Are you confused by the ENDS flavor debate? Dr. Ian Fearon, Broughton subject matter expert for clinical studies, has recently published an ...
US ENDS total flavor ban? Not quite.
January 3, 2020
The US Food and Drug Administration (FDA) has published final guidance regarding Enforcement Priorities for Electronic Nicotine Delivery ...
Broughton launch service to help determine impact ...
December 10, 2019
We’re delighted to announce that Broughton has recently launched an in-house service focused on enabling companies in the Electronic ...
Broughton research facility gathers pace with ...
November 19, 2019
We are delighted to announce that Broughton has made a series of major business transactions to meet the demands of our growing portfolio.
What does the Proposed Rule mean for ENDS ...
October 22, 2019
The US Food and Drug Administration (FDA) recently published a “Proposed Rule” for the Electronic Nicotine Delivery Systems (ENDS) sector. ...
ENDS HPHCs - What's new and why?
July 10, 2019
As we mentioned in our previous article, Final PMTA guidance has arrived – what’s changed?, FDA has modified the list of constituents or ...
Could clarity for US ENDS companies be imminent?
April 3, 2019
The latest statement from FDA Commissioner, Scott Gottlieb, outlines the agency’s actions to ensure sound regulation of tobacco products, ...
Latest guidance issued by FDA on requirements for ...
March 27, 2019
Tobacco product manufacturers are required to comply with certain requirements under Section 904(a) of the Federal Food, Drug and Cosmetic ...
Broughton expands its nicotine services business
March 21, 2019
We are delighted to officially announce the recent launch of Broughton Limited, a spin-off from the long-established Broughton. The new ...
Is a week a long time in the US ENDS industry?
March 14, 2019
It appears so, following a series of significant recent FDA announcements regarding Harmful and Potentially Harmful Constituent (HPHC) ...
Schedule a meeting with the FDA Center for ...
February 20, 2019
FDA regulated industries, including the ENDS industry, have few opportunities to engage with the FDA and receive valuable, bespoke product ...
What Every ENDS Company Should be Doing Leading ...
September 6, 2018
Save the date. Monday 22nd October is looking like a key day for the US ENDS industry.
E-cigarette Safety. The Evidence is Growing
July 5, 2018
Electronic cigarettes are battery powered electronic devices that enable delivery of nicotine to a user without the combustion processes of ...
Vape and the FDA Event Coverage
July 3, 2018
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 ...
How to Assess Your Contract Laboratory for HPHC ...
May 15, 2018
Maintaining regulatory compliance is a key factor in keeping your Electronic Nicotine Delivery System (ENDS) products on the market. A ...
FDA UPDATE - Extension of Certain Tobacco Product ...
November 14, 2017
The FDA has issued its latest guidance to the tobacco product industry, including Electronic Nicotine Delivery Systems (ENDS). The guidance ...
The PMTA Deadline is Now 2022. What Should I Do ...
August 10, 2017
On Friday, July 28th, the FDA issued a press release announcing the new plan for tobacco and nicotine regulation. There has been much ...
Tar Wars - Episode 2
July 26, 2017
With confusion and uncertainty on all sides surrounding the FDA regulations, the ENDS industry came together once again for the Vape and ...
Tar Wars - Episode 1
May 10, 2017
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
Key PMTA submission deadline – 30th June 2017
April 24, 2017
On May 10th, 2016, FDA issued a final rule extending its tobacco product authority to all tobacco products (except for accessories of ...
