The Testosterone Concierge

PSA TO CEOs & FOUNDERS OVER 40:

Here’s how to drop 20 lbs of fat, unlock 16 hours of persistent energy, and sleep 7 hours uninterrupted in the next 90 days:

A private virility system engineered for high-performance leaders. That’s it.

I reveal and deploy this system with you inside my private concierge program.

Within 90 days, you’ll:

- Lose 20 lbs of fat without fad diets or pill dependence.
- Sustain 16 hours of high-output energy daily.
- Sleep 7 hours straight, uninterrupted 

I launched this system in 2022 and since then have worked with dozens of founders, CEOs, and business owners. Here’s what it looks like:

- A 52-year-old exec added 3 hours of high-output work daily without stimulants.

- A real estate CEO lost 18 lbs of fat and reported “the best boardroom clarity in a decade.”

- A 47-year-old founder doubled stamina and dropped TRT reliance.

- A $100M portfolio leader said: “This gave me my edge back. My team can feel it.”

What clients say:

〽️ “This wasn’t a diet. My energy is back to my 30s, sustained for 16 hours a day.” – Jared Story, 8-Figure Construction Exec

〽️ “At 47, I thought decline was inevitable. In 120 days I lost 20 lbs of fat and now sleep 7 hours straight. Sharper, leaner, more present.” – Mark Follet, 7-Figure Business Owner

〽️ “The ROI is undeniable. Years of broken sleep gone, I now sleep 7 hours uninterrupted and added 3 more productive hours daily.” – Kieran Drew, 7-Figure Business Owner.

Ready to lose 20 lbs of fat, unlock 16 hours of persistent high-energy, and sleep 7 hours straight without interruptions in the next 90 days?

Book a private consultation to see if you qualify:

https://bit.ly/3VQqG8O

Founder, The Testosterone Concierge

CHEK Institute

HLC Certified Coach

iGNLP - International Guild of NLP

NLP Master Practitioner

Oxygen Advantage

Certified Coach

Hanson Wade

Commercial Director - LEAP HR

Senior Business Development Manager

Business Development Manager

Opus Talent Solutions 

Senior Consultant

Consultant

Dart Capital Ltd

Internship

GP Bullhound

I started working with CEOs and Founders over 40 in 2022 when I saw a simple truth:

Most high-performing men were carrying 20 extra pounds, running on fumes by 3PM, and waking up at 3AM staring at the ceiling. Exactly when their businesses and families needed them strongest.

By 2024, I had built a private virility system trusted by dozens of founders, CEOs, and business owners.

The results:

- 20 lbs of fat gone without fad diets or pill dependence.
- 16 hours of persistent energy from boardroom to bedtime.
- 7 hours of uninterrupted sleep every night.

Delivered in 90 days. Engineered for permanence, not gimmicks.

Now I work exclusively with 7–8 figure leaders who refuse decline. Men who know protecting their body and energy is protecting their legacy.

Here’s what that looks like:

- A 52-year-old exec added 3 hours of high-output work daily without stimulants or burnout.

- A real estate CEO dropped 18 lbs of fat while reporting “the best boardroom clarity in a decade.”

- 47-year-old founder doubled his stamina, rebuilt strength, and eliminated TRT reliance.

- A $100M portfolio leader said: “This gave me my edge back. My team can feel it.”

What clients say:

- “This wasn’t a diet. My energy is back to my 30s, sustained for 16 hours straight. At 52, I didn’t think that was possible.” – Jared Story, 8-Figure Exec.

- “At 47, I thought decline was inevitable. In 120 days I lost 20 lbs of fat and now sleep 7 hours straight. Sharper, leaner, more present at work and home.” – Mark Follet, 7-Figure Business Owner.

- “The ROI is undeniable. My sleep went from broken to 7 hours uninterrupted. I gained 3 more productive hours daily.” – Kieran Drew, 7-Figure Business Owner.

Ready to lose 20 lbs of fat, unlock 16 hours of persistent energy, and sleep 7 hours uninterrupted in the next 90 days using natural and sustainable methods?

Book a private consultation to see if you qualify.

https://calendly.com/your-simmo/consultationcall-with-simmo

(Disclaimer: My work is educational and coaching-oriented. It is not medical advice, diagnosis, or treatment, and does not create a doctor–patient or provider–client relationship. Always consult a qualified healthcare professional before changing any medication, supplement, or treatment)

Tom Simmons

Here2Grow Cosmetics & Homecare Labs 

✦I successfully achieved early adoption of CE Certification under the Medical Device Regulation (EU) MDR 2017/745 for a global market leader in Class I, Class II and III medical devices and life science products.  

✦ Technical documentation remediation, for product registrations in MENA, EMEA, APAC and US. Advising on Technical File composition and classification strategies. Coordinating and reviewing Product Information Files/Medical Technical Files/Labelling and Packaging. Supporting the management of product recalls, discontinuations and post market surveillance. Stakeholder management of Clinical Evaluation Reviews and Biological Safety Reviews.

✦ Supporting the reporting of serious adverse events; product recalls; the collection, and data analysis from external regulatory agencies or authorities; technical file reviews, gap analysis, technical file audit & remediation; proactive and reactive post market surveillance, stakeholder management.

✦ Delivering regulatory and compliance training/presentations to R&D, Innovation & QA/RA stakeholders, and brand owners

Director | Regulatory Compliance Consultant 

LifeStyles Healthcare

BRANDS: LifeStyles Condoms | Manix Condoms | LifeStyles Lubricants

✦ Providing regulatory consultancy support to LifeStyles Healthcare for their range of Condoms and Personal Lubricants

✦ Technical File remediation 

✦ Technical File Gap Analysis

✦ MDR 2017/745 Audit preparation

✦ General Product File compilation and remediation

✦ Product Information File compilation and remediation

Regulatory Compliance Consultant

Ansell

BRANDS: Encore Surgical Gloves | Gammex Surgical Gloves | Microflex Examination Gloves | Micro-Touch Examination Gloves 

✦  Led the successful CE Certification transition to the Medical Device Regulation (EU) MDR 2017/745 for Class I, II & Class III medical devices and  drug combination product

✦ Project management, technical documentation remediation, for product registrations in MENA, EMEA, APAC and US.

✦ Advising on Technical File composition and classification strategies.

✦ Labelling Regulatory Compliance and Artwork approval.

✦ Coordinating and reviewing Product Information Files/Medical Technical Files/Labelling and Packaging.

✦ Supporting the management of product recalls and post market surveillance.

✦ Stakeholder management of Clinical Evaluation Reviews and Biological Safety Reviews.

BRANDS:  Durex, Veet, Clearasil, Lemsip, Nurofen, Strepsils, Mucinex

✦ Relationship management of key stakeholders including Scientific Services Group, Supply, R&D, Clinical, Procurement and external contractors.  

✦ Developed new Reg Excellence processes and strategies for EU regulation 1223/2009 implementation.  

✦ Authored and developed SOPs, gap analysis methodologies, databases and training tools. 

✦ Regulatory compliance, composition and authoring of PIFs and eCTDs for 80+ products.

✦ Project coordination of statutory reporting requirements and notification.

✦ Facilitated audit and inspections by the MHRA and IMB.

Global Regulatory Associate | CCDS Project Coordinator

KidooLand "La petite école anglaise"​ enseignement en anglais créatif & positif

✦ Teaching English as a second language to pre-school children 

✦ Private English language tuition 

✦ Teaching English in a private language school

✦ Teaching English in a public French school

✦ Freelance English language tuition to private students.

Professor D'Anglais at KidooLand | TESOL Teacher 

Renew

✦ Leadership and co-ordination of a multi-agency partnership, working with stakeholders from health, police, education, economic development, housing and elected representatives.

✦ Led the development of a regeneration strategic framework and branding strategy.

✦ Redesigned policies and practices to drive the regeneration process.

✦ Chaired and coordinated stakeholder meetings and working groups.

✦ Rolled out a programme of community capacity building events and consultations.

✦ Researched and analysed economic, enterprise and employment opportunities.

Partnership Manager

Manchester City Council

✦ Project managed social marketing initiatives in collaboration with the Department of Health as part of the national Communities for Health Programme. 

✦ Designed, planned and facilitated global conferences, road shows and workshops for 100+ participants. 

✦ Worked collaboratively with authorities and stakeholders across the UK, EU and China.  

✦ Supported the implementation of local plans for neighbourhood renewal, through Local Strategic Partnerships.

✦ Audited and monitored programme delivery for £150m capital programme against government targets and KPIs.

✦ Programme performance and risk reporting to Department for Communities and Local Government.

Project Coordinator | Programme Officer 

Salford City Council

✦ Monitored the implementation and delivery of ERDF Objective 2 Programme: Improving Access to Employability.

✦ Prepared and submitted SRB, ERDF, English Partnerships, North West Development Agency 
proposals.  

✦ Analysed & monitored performance against benchmarks and targets, including presentation of reports and papers to Cabinet and Working Parties.

✦ Submitted proposals and reported financial performance to EU authorities.

Senior Finance & Administration Officer

Summary: 

✦ I provide tailored solutions to address your regulatory compliance challenges, developing practical and effective strategies to bring your cosmetics, medical devices and homecare products to market in the UK, EU, and globally.

Experience: 
✦I have over 12 years of regulatory consultancy experience, supporting global companies with cosmetics compliance and Medical Device CE marking.

Industries: 
✦ I have global experience across MedTech, Life Sciences, FMCG, Cosmetics/Personal Care, and Homecare industries.

Markets: 
✦ My market experience includes, compliance for EMEA, APAC, ANZ and MENA 

Product Classification Expertise:
✦ Class I, II & III Medical Devices, Medicinal Products, Cosmetics, PPE

Expertise:
✦ Cosmetics Regulation (EC) 1223/2009
✦ Medical Devices Regulation (EU) 2017/745
✦ Medicinal Products Directive 2001/83/EC
✦ UK Medical Devices Regulations 2002
✦ Classification determination
✦ Technical file audit and remediation
✦ Declaration of Conformity
✦ Post Market Surveillance
✦ Product Recalls
✦ Clinical Evaluation Reviews
✦ Biological Safety Reviews
✦ PIFs
✦ Gap analysis
✦ CLP
✦ Product registration
✦ PIF compilation
✦ Common Technical Dossiers
✦ Facilitating Audits
✦ Training and presentations

Standards Expertise:
✦ ISO 9001 Quality Management System
✦ ISO 13485 Medical Devices - Quality Management Systems
✦ ISO 14971 Application of Risk Management to Medical Devices

✦ CONTACT ME: vbrew@here2grow for a FREE Discovery call

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Tom Simmons

Vinetta Brew

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