Still Trying Medication After Medication, Hoping This One Finally Works?
Discover which medications are right for YOUR body in weeks, not years with a simple at-home test you'll never need to repeat. Up to 30% of patients experience poor response or side effects from common medications. The problem isn't the drug, it's the mismatch between the drug and your genes. Now there's a faster way to know what drugs your body can and cannot metabolise and at what dose! No more guess work.
30-Day Clarity Guarantee | Delivered in 3–4 Weeks From Test Batch Processing | Lifetime Value
Get your comprehensive clinical report covering 70–80 medications for now and your future.
Saliva test kit delivered to your door, analysed by experts, results are yours for life.
FOR ONLY £350
£5,500+ in potential savings
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What's Included In Your Personal
Medication Blueprint?
The NPH Group-PGx test is the fastest way to understand which medications actually work for YOUR body without years of trial and error, debilitating side effects, or feeling like a guinea pig in someone else's experiment.
Because let's face it, you already know medications can work.
You've seen other people find relief. You've heard your GP say "this one helps most patients."
You've probably even hoped that THIS time, things would be different…
But the part nobody talks about?
Up to 30% of people don't respond normally to common medications.
Not because the drugs are bad. Not because you're doing something wrong.
But because your genes process them differently than the "average patient" your doctor's guidelines were written for.
And that's why you've been stuck.
Trying one drug after another. Waiting months to see if it works. Dealing with side effects that sometimes feel worse than the condition itself. All while wondering if maybe, just maybe, the problem is you.
It's not. The problem is that nobody's ever looked at your genetic blueprint. Until now.
NPH Group-PGx flips the script on trial-and-error prescribing. Instead of guessing which medications might work and hoping for the best, we analyse the specific genes that determine HOW your body metabolises drugs across three critical categories:
- Heart conditions and blood pressure
- Chronic pain management
- Depression and anxiety
The result? A comprehensive clinical report written in plain English, not scientific jargon that tells you and your GP:
- Which medications are likely to work well for your body…
- Which ones carry a higher risk of side effects or poor response…
- And specific dosing considerations that could make all the difference…
This isn't another generic health test that leaves you with more questions than answers.
This is precision medicine, the same approach used by leading healthcare systems worldwide delivered accessibly by an established UK clinical provider you can actually trust.
30-Day Clarity Guarantee | Delivered in 3–4 Weeks From Test Batch Processing | Lifetime Value
Here's What Changes When You Have
Your Medication Blueprint:
- The exact genetic markers that reveal how your body processes 70–80 validated medications, no more guessing, no more hoping…
- Clear, GP-ready recommendations so your doctor can make informed decisions based on YOUR biology, not population averages…
- Validation that previous failures weren't your fault, finally understand WHY certain drugs never worked, even when they "should have"…
- Confidence walking into every GP appointment with real data instead of vague symptoms and crossed fingers…
- A lifetime gene profile that generates new reports whenever your medications change, you test once, you benefit forever
- Complete data ownership, your genetic information stays yours, stored securely in the EU, never shared without your explicit consent…
The science behind pharmacogenomic testing has been researched for decades. It's already used in major healthcare systems worldwide, including FDA guidance in the United States.
Large-scale studies show it saves an average of £5,500 per patient by eliminating failed treatments, reducing side effects, and cutting avoidable healthcare costs.
This isn't experimental. This isn't fringe. This is proven precision medicine that the NHS will likely adopt in the coming years.
We're simply making it available to you NOW, instead of asking you to wait while your health suffers.
And unlike faceless online labs that send you a kit and disappear, NPH Group is an established occupational health provider with nearly a decade of experience supporting real healthcare decisions. We're CQC registered and SEQOHS accredited, the gold standards for clinical quality in the UK.
When you receive your report, it's not auto-generated by an algorithm. It's clinically interpreted by experts who understand what the results actually mean for YOUR situation.
Once you receive your Personal Medication Blueprint, everything changes.
That foggy uncertainty about whether your meds are right? Gone.
That anxiety before every GP appointment? Replaced with confidence.
That nagging feeling that you're missing something? Finally addressed.
Because for the first time, you'll walk into your doctor's surgery with evidence. Real genetic data that explains why certain drugs haven't worked and which ones are more likely to.
Your GP doesn't have to guess anymore.
And neither do you. Instead of another round of "let's try this and see how you get on," you'll have an informed conversation about options that actually fit your biology.
Which means faster relief. Fewer side effects. And finally, FINALLY a path forward that's based on science, not hope.
This is how you stop being a guinea pig and start being in control of your own healthcare.
30-Day Clarity Guarantee | Delivered in 3–4 Weeks From Test Batch Processing | Lifetime Value
Everything You Receive With Your
NPH Group PGx Test
At Home Test Kit Posted Directly to Your Door
No clinic visits, no waiting rooms, no time off work. Complete the simple cheek swab in seconds and post it back in the prepaid envelope.
Accredited Laboratory Analysis
Your sample is processed in a specialist pharmacogenomics laboratory with the highest chain of custody documentation. Your unique gene profile is extracted and stored securely.
Comprehensive Clinical Report
Covering 70–80 validated medications across heart conditions, chronic pain and mental health. Written in plain English with specific recommendations you and your GP can act on immediately.
GP Consultation Guidance
Clear talking points and precise questions so you can have a productive conversation with your doctor, even if they've never seen a pharmacogenomic report before.
Lifetime Gene Profile
Stored securely in the EU under GDPR protection. Your genes don't change, so you never need to retest. Request additional 'tailored' reports for new medications when they become available and wherever needed for a smaller additional charge.
Optional Clinician Support
For those who want extra guidance, NPH Group clinicians are available to walk through your results and help you prepare for your GP appointment for an additional fee for private nurse and GP consultations, if needed.
How Does Your Personal Medication
Blueprint Work?
Get clarity on which medications fit YOUR body in just 4 simple steps…
- 01
Order Your At Home Kit
Place your order and your test kit arrives within days with everything you need included. No clinic visits required.
- 02
Collect Your Saliva Sample
A quick cheek swab takes seconds. Seal it in the envelope provided and pop it in the post. That's it, you're done.
- 03
Clinical Report Within 3–4 Weeks
You'll receive a comprehensive report explaining exactly how your genes affect your response to 70–80 medications. Plain English. Specific recommendations. GP-ready.
- 04
Take Informed Action
Book an appointment with your GP, share your report, and have the conversation you've been waiting for. For the first time, decisions will be guided by YOUR genetic profile, not trial and error.
30-Day Clarity Guarantee | Delivered in 3–4 Weeks From Test Batch Processing | Lifetime Value
What UK Organisations are Saying About
NPH Group's Solutions
We are really pleased with the excellent service provided by NPH Group. As a new client, three years ago, we were welcomed with an overview of the comprehensive range of services and how to access these. It is evident that the systems and processes have been tailored to make accessing these services very straightforward. I am always struck by the clarity and helpfulness of all the staff at NPH Group. The medical reports we receive are clear and concise and support the College in addressing cases of sickness absence.
What's really good is the instant issue of the reports. Love that, as with the previous company we used it took weeks! We have had a great service to date so please let your team know this and do keep up the good work.
The customer support is great within NPH Group. When I call up about a query, I am not waiting very long and the issue always gets resolved. Everyone is so friendly and always willing to help. I believe it is 10/10 customer support.
The service enables us to take a proactive approach in the management of employees who are far from ill health, enabling us to move issues forward with the support of 1st class professional medical opinions. We are pleased with the results we have achieved from the service and believe that their interventions have significantly contributed to a 50% reduction in our overall absence levels over recent years.
Thanks to the support of the NPH Group, particularly since Covid-19. The team always reply quickly when I'm asking for urgent support. I never have any worries that someone won't get back to me and they always do their best to meet our needs. They are great team.
Frequently Asked Questions
Need Help? Email us: info@nph-group.co.uk
Why isn't my GP already doing this?▾
Great question! and one we hear often. Pharmacogenomics has strong evidence behind it and is already used in major healthcare systems worldwide, including FDA guidance in the US. But NHS implementation takes time. We're simply making it accessible now, rather than asking you to wait years for widespread adoption. Think of it like private healthcare: the same quality of care, just available sooner.
£350 feels like a lot, what if it doesn't change anything?▾
We understand. But consider what you've already spent on medications that didn't work, GP appointments that led nowhere, and time lost to side effects and poor symptom control. £350 is less than a single private consultant appointment, yet delivers clarity you'll use for the rest of your life.
And here's the thing: even if your report confirms your current medications ARE well-matched to your genetics, that's enormously valuable. It eliminates the exhausting "what if something else would work better?" doubt and gives you peace of mind. Plus, your lifetime gene profile is ready for whenever future medications arise.
Research shows pharmacogenomic-guided prescribing saves an average of £5,500 per patient. This isn't a cost, it's an investment that pays for itself many times over.
Is it safe to have my genetic data stored? Who can see it?▾
Your genetic data belongs to YOU. Full stop. It's stored securely in the EU under GDPR protection and is never shared with employers, insurers, or any third party without your explicit written consent. You can request deletion at any time (though future call-off reports wouldn't be possible). NPH Group is CQC registered and SEQOHS accredited, we take data protection as seriously as clinical quality.
Will my doctor actually use the report, or just ignore it?▾
Your report is written in clinical language GPs understand, with specific recommendations they can act on. It's not a replacement for their professional judgement, it's additional evidence to inform their prescribing. Most doctors welcome more information, especially when it explains why previous treatments failed. The report includes clear talking points for your GP conversation, and if you want extra support, our clinicians can help you prepare for the appointment.
What if my genes show bad news?▾
This test doesn't tell you what's wrong with you. It tells you what's RIGHT and which medications actually fit your body. There's no "bad" result. Either you discover why certain drugs haven't worked (and which ones are more likely to, perhaps even with a change of dose based on the report your gene findings), or you confirm your current medications are well-matched. Both outcomes give you clarity and control you didn't have before.
Is pharmacogenomics actually proven, or is this experimental?▾
Pharmacogenomics has been researched for decades. It's not new or experimental, it's an established field of precision medicine already used in major healthcare systems worldwide. The FDA includes pharmacogenomic information in the labelling of hundreds of medications. Large-scale studies demonstrate significant cost savings and improved outcomes. We're not asking you to bet on something unproven. We're offering established science, delivered accessibly.
PGx services are currently available in Holland for example, with virtually all pharmacies having access to personal test data to help inform precisions prescribing. The UK is just behind the curve and we don't have the money to make it widely available publicly as a society.
Who Is Mark Philpott & NPH Group?
NPH Group has been operating in the occupational health space for nearly a decade supporting real healthcare decisions in real workplaces across the UK.
We're not a faceless online lab that sends you a kit and disappears. We're an established clinical provider with:
- CQC Registration meeting the Care Quality Commission's standards for healthcare quality
- SEQOHS Accreditation, the gold standard for occupational health services in the UK
- A multi-disciplinary clinical team including occupational health physicians, nurses, and technicians
- Deep experience in safety-critical environments where getting medication right isn't just about comfort, it's about safety
Over the years, we've seen the same pattern repeat across industries: employees struggling with medications that don't work, employers paying for support services that never address the root cause, and everyone stuck in a cycle of trial-and-error that costs time, money, and quality of life.
That's why we partnered with a specialist pharmacogenomics laboratory to bring precision medicine into everyday healthcare, at home, and in the workplace.
What makes NPH Group different?
We don't just send you data and wish you luck. We provide clinical interpretation expert analysis that translates your genetic profile into actionable recommendations your GP can use immediately.
We don't disappear after the test. Your gene profile is stored securely, and we're here whenever you need additional reports or clinical support.
And we're not asking you to trust a startup with your genetic information. We're an established provider with nearly a decade of clinical experience and the accreditations to prove it.
This is precision medicine, delivered properly.
The Clarity Guarantee
We believe everyone deserves to know how their body processes medication. That's why we've removed every barrier to getting clarity.
Here's our promise:
- Your NPH Group PGx test will deliver a comprehensive clinical report covering how your genes affect your response to 70–80 validated medications.
- If your report contains no actionable insights relevant to your current or potential medications meaning there's genuinely nothing to inform your GP conversations, contact us within 30 days and we'll discuss your individual situation directly with our clinical team at no additional charge.
We can offer this because the science works. Your genes DO affect medication response.
The only question is which insights are most relevant to your situation and we'll help you understand.
Best case: You receive your report and discover exactly why certain medications never worked for you. You share the findings with your GP, adjust your treatment, and within weeks experience better symptom control with fewer side effects.
For the first time, you feel confident you're on the right path and you have a lifetime gene profile to guide every future medication decision.
Worst case: Your report confirms that your current medications are already well-matched to your genetics. No changes needed. You've spent £350 to gain peace of mind and eliminate uncertainty, plus you now have a lifetime gene profile ready for whenever future medications arise.
Either way, you win.
Here's Everything You Get:
- At-home test kit delivered to your door
- Accredited laboratory analysis with full chain-of-custody
- Comprehensive clinical report covering 70–80 medications
- Plain English explanations with GP-ready recommendations
- Lifetime gene profile stored securely in the EU
- Future call-off reports available whenever needed
- 30-Day Clarity Guarantee
Total Investment: £350
(Less than a single private consultant appointment, for clarity you'll use the rest of your life)
30-Day Clarity Guarantee | Delivered in 3–4 Weeks From Test Batch Processing | Lifetime Value
Still Wondering If This Is Right For You?
This is for you if:
- You're currently taking medication for heart conditions, chronic pain, or depression/anxiety
- You've tried multiple drugs that haven't worked or caused significant side effects
- You're frustrated by the trial-and-error approach and want evidence-based clarity
- You're willing to invest in your health when you believe it will actually work
- You want to share findings with your GP and take informed action
This is NOT for you if:
- You're not currently on medication and have no plans to be
- You're looking for a magic solution that requires no action from you
- You won't share results with your GP or healthcare provider
- You believe genetic testing is fundamentally unsafe regardless of safeguards
The Cost of Waiting
Every month on the wrong medication is another month of side effects, poor symptom control, and lost quality of life.
Every "let's try this instead" conversation is another three to six months of uncertainty.
Every year that passes is another year of your life spent as a guinea pig in someone else's experiment.
For £350, less than a single private consultant appointment, you could have clarity THIS month instead of spending another year guessing.
The question isn't whether pharmacogenomics works. The research shows it does.
The question is: how much longer are you willing to wait for answers your genes already hold?