Staying on top of regulatory changes, new technical innovations, and industry-disrupting competitors has never been harder. With so much information available, how do you ensure you have the insight you need to drive your business forward and seize opportunities before the competition?
Our regulatory and scientific experts are here to help you stay up to speed with new trends and research. Let them share their expertise and insight so you can focus on building your business.
Streamlining the PMTA process for oral nicotine products with tailored strategies and efficient project management.
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Accelerate your nicotine pouches to market with Broughton's comprehensive full-service solutions. This guide details our nicotine pouch testing and additional toxicology packages.
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Are you a category innovator developing heated tobacco products (HTPs) to help achieve a smoke-free future? Read our expert advice on navigating the regulatory landscape to bring a heated tobacco product to market.
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Broughton is a leading global contract research organisation specialising in tobacco harm reduction, medicinal cannabis, cannabinoids, and pharmaceuticals, we can help bring category innovators life-enhancing products to market.
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New product research requires deep scientific understanding to ensure these products are regulatory compliant and accepted by consumers. Broughton are experts in bringing NGPs to market.
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With over 60,000 liters of in-house ICH stability storage capacity, supported by a team of highly qualified scientists and GMP-accredited laboratory testing facilities, we have approximately 250 live studies in progress and offer a full range of stability services to help bring your product to market or ensure its ongoing compliance requirements.
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Discover how Broughton leads in supporting HTP manufacturers for tobacco harm reduction.
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At Broughton, our consultants have deep industry knowledge across all the elements required for a PMTA. We guide you through and generate the required data, to ensure that FDA finds your applications strong and compelling.
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An overview of the Tobacco Products Directive and Tobacco-Related Products Regulations. Get the straightforward answers you’re looking for when it comes to TPD and TRPR analysis.
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Looking to take your ENDS products to new markets? Compare the differences and get the pros and cons between products with EU Tobacco Products Directive (TPD) notification and products with an EU medicinal product license in our free download.
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We help companies of all sizes through the product lifecycle stages, from concept innovation, product realization, and regulatory submission to post marketing surveillance.
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The evaluation of extractables and leachables (E&L) is an essential component of the pharmaceutical development process.
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Our team of in-house toxicologists reviews and evaluates toxicological data on a wide range of chemicals to produce independent expert opinions on risk assessment. We then advise on the strategies to mitigate or reduce those risks to protect corporate reputation and public health.
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Our product development and regulatory experts can help you meet expectations at key milestones in your product development project to better inform decision making and investment choices.
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Learn about six easy-to-spot packaging violations that could indicate a vape is illicit and shouldn't be on sale in the UK and EU.
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We believe that the sectors we work within expect a continually improving service where we constantly strive to improve processes and Quality.
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ToxHQ by Broughton offers automated, data-driven risk assessments and delivers fast, high-quality toxicological evaluations, so you can launch safer products with confidence.
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Explore HTP Regulations and Testing in our scientific poster presented at CORESTA's Annual Congress and the Tobacco Science Research Conference
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In this whitepaper, we discuss the stability studies that may be performed during pharmaceutical development and in support of a regulatory dossier to support the licensing of a medicinal drug product.
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The US FDA has granted Marketing Orders for four menthol-flavoured pe-cigarette products. This marks the first time that the FDA has granted MOs for non-tobacco flavoured products via the PMTA pathway.
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Product Lifecycle Manager, Malcolm Saxton was featured in the June edition of NGP Trends discussing the most effective way to design a heated tobacco product.
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There is no doubt that the reduced-risk industry today is at an impasse, although there is now common acceptance that combustible cigarettes are the most hazardous form of nicotine delivery due to the accompanying harmful chemicals produced from tobacco combustion.
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Rishi Sunak recently announced that the UK Government would ban disposable vapes as part of its plan to tackle the rise in youth vaping. Paul Hardman shares his thoughts on the announcement and what may come next.
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Broughton share their thoughts on how to reduce costs and protect timelines while continuing to innovate.
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Our Senior Consultant, Malcolm Saxton presented a poster at the 76th Tobacco Science Research Conference in Norfolk, Virginia USA about ‘E-Cigarette Regulatory Non-Compliance in the UK Marketplace’.
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The adaptation of e-cigarettes as drug delivery devices holds great potential for inhalation therapy. So, can we apply the advances made in nicotine delivery to other active substances?
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The UK heated tobacco market continues to evolve rapidly, with growing consumer interest and an increasingly competitive landscape.
The Ministry of Industry and Advanced Technology (MoIAT) has recently issued the Final Draft Standard (FDS) UAE.
The nicotine pouch market in the US is growing rapidly, but so is regulatory scrutiny.
Arrange a meeting with a scientific or regulatory expert to discuss your project and learn how we can help accelerate your product to market to maximize your success.
