Broughton gains new regulatory insight while ...
May 18, 2022
Broughton celebrates Premarket Tobacco Product Application (PMTA) success for clients.
Broughton's Chief Scientific and Regulatory Officer Dr. Nveed Chaudhary discusses the recent FDA announcement on marketing orders and what ...
Is England going far enough to be smoke-free by ...
April 26, 2022
Broughton's Chief Scientific and Regulatory Officer Dr. Nveed Chaudhary discusses how England is leading the way internationally in terms ...
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 ...
The end of e-cigarette regulation uncertainty in ...
January 12, 2022
Broughton's Head of Regulatory Affairs, Lloyd Smart, and Regulatory Consultant, Xiangyin Wei summarise China's Tobacco Monopoly Law Changes ...
What manufacturers should know about the medical ...
December 3, 2021
Broughton's Head of Regulatory Affairs, Lloyd Smart has recently published an article with the leading sector publication Tobacco Reporter.
The race to register e-cigarettes as medicinal ...
November 30, 2021
Broughton's Chief Scientific Officer, Chris Allen shares his opinion with Financial Times about e-cigarettes on the NHS.
UK MHRA announce the latest guidance on ...
October 29, 2021
Broughton's Head of Regulatory Affairs, Lloyd Smart discusses the latest UK Medicines & Healthcare products Regulatory Agency (MHRA) ...
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 ...
Australia tightens existing nicotine vaping laws ...
October 12, 2021
Broughton's Head of Regulatory Affairs, Lloyd Smart discusses the Australian Government's recent announcement regarding existing nicotine ...
We’ve officially left the EU, but what does ...
May 13, 2021
Broughton Director of Product Safety and Compliance, Yvonne Wilding, discusses implications of Brexit on the international ENDS market.
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 ...
Innovate to accelerate. Blue-sky thinking hub.
March 30, 2021
Broughton Chief Regulatory Officer, Dr Nveed Chaudhary announces the launch of our Blue-sky thinking hub aimed at nicotine, pharmaceutical, ...
What’s next for Tobacco Use and Next Generation ...
March 5, 2021
Broughton Dr Nveed Chaudhary, Chief Regulatory Officer discusses the EU's stance on Next Generation Products and what this means for ...
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 ...
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 ...
Potential delay to Revision of the Tobacco ...
October 1, 2020
Emily Saunders, Regulatory Operations Manager, takes a look at the potential delay to the Tobacco Product Directive (TPD3) and the future ...
Hot Topic - Comparative Regulations, GTNF 2020
September 14, 2020
Broughton announce, Chief Scientific Officer to join panel discussion at GTNF 2020
Elemental Analysis of e-Cigarettes: Pushing the ...
September 11, 2020
Broughton, Senior Project Scientist, will participate in a webinar hosted by Separation Science, sponsored by Thermo Fisher Scientific.
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 ...
Broughton explain the importance of ...
August 19, 2020
Broughton are pleased to take part in Thermo Fisher Scientific’s video series - Charlie Chats.
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.
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. ...
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 ...
