Blog: Our Insights
Your resource for industry news and updates from Broughton.

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 ...

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 ...

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 welcomes Paul Hardman as our new Head ...

May 6, 2021

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 ...

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 ...

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

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 ...

Blog: Safety Evaluation of Extractables and ...

July 23, 2020

Broughton announce new webinar.

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.

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 ...

US ENDS market at its crossroads

December 16, 2019

Turn left or turn right?

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 ...

Join us at ENDS US 2019

November 26, 2019

ENDS US 2019 is the ideal place to keep up with the ever-changing knowledge base required to operate in the nicotine products industry; the ...

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 ...

ENDS 2017

June 15, 2017

The key strapline echoed by many key figures within the industry was ‘the FDA regulations are here to stay, and we just have to deal with ...
Contact us

From basic questions to complex compliance inquiries, we're here to help! Contact us today.