Regulatory & Compliance

NADCLINICPRO was created for clinics and healthcare professionals who require medical-grade NAD+ solutions and clear, understandable regulatory frameworks in order to operate responsibly, safely, and long term.

This page explains where and how NADCLINICPRO can be used, and how we support our partners in navigating professional, legal, and operational expectations — without regulatory grey zones or uncertainty

NADCLINICPRO products are developed for professional clinical and medical environments and manufactured according to pharmaceutical-grade quality and quality-assurance principles.

Our partners typically choose NADCLINICPRO because they:

• require medical and clinical quality standards

• do not wish to work with consumer-level "wellness" products

• seek a professionally and legally defensible operating framework

NADCLINICPRO does not position NAD+ as a consumer wellness supplement.
Our focus is practitioner-led, professional use.

NADCLINICPRO operates with active awareness of internationally recognised quality and regulatory frameworks, including:

• GMP-aligned manufacturing principles

• USP (United States Pharmacopeia) quality references

• European Pharmacopoeia (Ph. Eur.) standards

• Region-specific healthcare and facility regulations

This approach allows partners to work within structured, defensible professional frameworks, rather than uncertain wellness positioning.

🇪🇺 European Union (EU)

Simply explained:
 In the EU, NADCLINICPRO is designed to work best in physician-led clinical environments.

• Practitioner responsibility is central

• Ph. Eur. and GMP principles are respected

• No treatment or outcome claims are made

This enables responsible clinical integration within EU regulatory expectations.

🇭🇺 Hungary – An Established Partner Model

In Hungary, NADCLINICPRO already works with existing clinical partners.

How it works in practice:

• NAD+ is applied within physician-led or licensed healthcare settings

• Clinical decisions remain with the healthcare professional

• Products are integrated according to medical-grade expectations

This represents a proven, operational reference model that informs expansion into other markets.

🇬🇧 United Kingdom (UK)

Simply explained:
 In the UK, the key is strict, compliant communication.

• Practitioner-controlled decision-making

• No exaggerated claims

• Clear separation from consumer wellness marketing

This protects professional accountability and clinical integrity.

🇺🇸 United States (US)

Simply explained:
 In the US, NADCLINICPRO operates within a professional-use framework.

• USP-referenced quality thinking

• FDA-aware positioning

• All clinical decisions remain with licensed physicians

This approach helps reduce regulatory and legal risk.

🇦🇪 United Arab Emirates (UAE)

Simply explained:
 In the UAE, NADCLINICPRO is well suited for licensed medical clinics.

• Facility and practitioner licensing is required

• Premium medical environments are expected

• Clear separation from wellness-only offerings

This aligns well with DHA / DOH-style regulatory environments.

🌏 Asia-Pacific (APAC)

Simply explained:
👉 In Asia, regulations vary by country — flexibility is essential.

• Consistent medical-grade quality expectations

• Support for local regulatory interpretation

• Adaptable professional framework

This allows responsible integration across diverse APAC markets.

NADCLINICPRO does not distance itself from responsibility —
nor does it exceed regulatory boundaries.

NADCLINICPRO provides:

• Medical-grade product quality

• Regulatory-aware positioning

• Structured integration frameworks

• Professional communication guidelines

Partners retain responsibility for:

• Clinical decision-making

• Local regulatory compliance

• Professional and patient responsibility

This balance enables safe, sustainable, long-term partnerships.

To protect both the brand and its partners, NADCLINICPRO

• does not make diagnostic or therapeutic claims

• does not promise guaranteed outcomes

• does not replace professional medical judgment

All communication is designed to remain:

• ethical

• science-informed

• compliance-aligned

• professionally defensible

this framework allows professionals to work with medical-grade NAD+ without unnecessary risk.

It enables partners to:

• maintain professional credibility

• avoid regulatory grey zones

• focus on patient care rather than legal uncertainty

This approach allows clinics and healthcare professionals to work with NAD+ confidently, ethically, and responsibly.