News & Insights

If you’ve never launched in the UAE before, this bit can catch you off guard. It’s not just about ticking a few extra boxes. It’s about understanding the local laws and making sure you’ve got the right people backing you so your product doesn’t get stuck in limbo at customs.

We built Taylored Training to be none of those things.When you work in cosmetics, supplements, or medical devices, you can’t afford to not understand the regs. But you also don’t have time to become a full time compliance expert. That’s where we come in.

The line between wellness products and medical devices is getting messier by the minute. Think fitness trackers. Period pain relief devices. Meditation headbands. Blue light masks. Sleep tech. They look like lifestyle products. They’re sold in beauty halls. But depending on what they do and more importantly, what you say they do, they might fall squarely under medical device regulations.

Let’s not beat around the bush: the wellness industry loves a bold claim. And testosterone boosters are having a bit of a moment. Whether it's TikTok influencers promising god-tier gains or supplement brands casually implying you’ll wake up looking like Jason Momoa, there’s a lot of hype.

So here’s your quickfire, regulator-with-a-heart breakdown of what you need to know about 1st and 2nd generation hayfever meds, and why it actually matters for you as a consumer.

It always starts the same way: a ‘beauty hack’ goes viral, a few influencers jump on it, and suddenly every indie brand with a Shopify account is repurposing a product to “ride the trend.” We get it. It’s tempting.

If you're adding essential oils to a cosmetic product in the UK or EU, it's not as simple as picking your favourite scent and pouring it in. You’re dealing with complex chemical mixtures that need to be understood, assessed, and used with caution.

In the landscape of consumer safety and regulatory compliance, the UK Responsible Person plays a pivotal role in ensuring that products placed on the market meet the necessary standards and requirements.

Marketing medical devices can be a challenge. The Advertising Standards Authority (ASA) and Committee of Advertising Practice (CAP) shape the rules for advertising in the UK, including what you can and cannot say about medical devices.

In the bustling world of health and wellness, food supplements have become an integral part of many individuals' daily routines. Whether it's bolstering essential nutrients or supporting specific health goals, the demand for these products continues to soar.

The UK's regulatory environment for medical devices has evolved over the years. Historically, we followed the European Union's Medical Device Directive (MDD). However, post-Brexit, we have established our own regulatory system.

You might assume that all sun creams are just… cosmetics with SPF slapped on the label. But that’s not always the case.

Whether you're launching your own fragrance or just curious about what’s behind that fancy glass bottle, here are five compliance and regulatory facts about perfume that might surprise you.

Scroll through TikTok or Instagram and you’ll find countless influencers and “wellness experts” raving about its benefits, from better sleep and reduced anxiety to improved focus, mood, hormone balance, digestion, and basically everything else under the sun.

So let’s talk about it from a regulatory perspective. Because while celebrity brands often get the spotlight, they’re still held to the same standards as everyone else. Or at least… they should be.

But here’s the problem: not all sleep supplements are created equal, and in many cases, they’re not as well-regulated as they should be

Whether you're launching a cosmetic, medical device, or food supplement, the registration process is where most brands either get it right… or get stuck. Here are three key steps to follow, and three common mistakes to avoid, so you can get your product to market without delays, drama, or unnecessary risk.

It's Valentine's Day, so let’s talk about intimate wellness products and the fine line between a cosmetic, a general consumer good, and a bona fide medical device. Whether you're treating your partner to something special or launching a new product in the booming personal wellness market, knowing the regulatory landscape is key—because getting it wrong can mean compliance nightmares, product recalls, or even market bans

Developing a product is no small feat—countless hours, resources, and passion go into bringing an idea to life. But what happens when the regulator says, “Not approved”? It’s a situation no one wants to face, but it’s not the end of the road. Here’s how to move forward strategically, preserve your investment, and rebuild for success.

lapping a “biodegradable” label on your packaging doesn’t always mean what you think it does. As consumers become more eco-conscious, brands are leaning into sustainability claims, but not all of them hold up under scrutiny.

Let’s talk about the Period After Opening (PAO) symbol. You’ve probably seen it—the little open jar with a number and an “M” on it. It’s not just there to make the product look more official; it’s actually one of the most important pieces of info on your cosmetic product.

Let’s talk 2025 and what’s coming for medical devices, food supplements, and cosmetics. The regulatory world isn’t slowing down, and if you’re in these industries, there are some changes on the horizon that you really need to care about.

On September 25, 2024, the Food Standards Agency (FSA) and Food Standards Scotland (FSS) issued important guidance on caffeine in food supplements. This new guidance aims to promote safe consumption and manufacturing practices for supplements containing high levels of caffeine.

For manufacturers, importers, and distributors of medical devices, understanding the difference between CE and UKCA markings is vital. These marks signify compliance with specific standards and ensure the safety and efficacy of medical products in their respective markets.

Ashwagandha, known scientifically as Withania somnifera, is an adaptogenic herb traditionally used in Ayurvedic medicine where it is used to treat conditions including rheumatism, digestive issues, insomnia, and joint inflammation.

If you want to sell medical devices into the European (EU) marketplace, you need to understand the role of an EU Authorised Representative. Our job is to act as the key person connecting non-EU manufacturers with European regulatory authorities making sure they follow EU rules.

Since Brexit, importing goods into Great Britain has completely changed bringing with it a labyrinth of new regulations and standards impacting the smooth operation of businesses dealing in dietary supplements, food supplement, vitamins, and other nutrition-focused products.

In recent years, there has been a growing interest in the use of food supplements to enhance cognitive function and focus. With the rise of fast-paced lifestyles, influencers touting bio-hacking techniques and optimal performance, and an increasing awareness of the importance of mental well-being, consumers are seeking products that claim to help improve their cognitive abilities. However, for food supplement companies looking to make claims about improving non-medical effects like focus and cognition, navigating regulatory requirements can be a complex and challenging task.

Labelling cosmetic products is an essential part of product compliance. The UK has strict regulations so understanding the nuances of when it comes to creating labels for your cosmetics is really important.

Medical device registrations and regulations are ever evolving so understanding how a UKRP can help has become a really important part of post-Brexit processes.

It's with immense joy and gratitude that Taylored Consultancy celebrates 1 year in business. What a remarkable journey it has been!