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UK BRCGS & GMP Certified Lab

Product Development

Bespoke New Product Development (NPD) & Custom Formulation Services for Global Supplement Brands & B2B Distributors.

Expert NPD Services

Transforming Your Concept into a Market-Ready Supplement Brand

Nutribl offers a dedicated New Product Development (NPD) service designed specifically for brand owners, pharmacies, clinics, and international procurement partners seeking unique, commercially viable food supplement formulations.

Developing a successful bespoke supplement requires precision, market foresight, and technical expertise. Our in-house team of formulation scientists and regulatory experts bridges the gap between your brand vision and compliance with stringent UK, EU, and global food safety standards.

Full-Spectrum Technical Support

  • Custom Recipe Engineering: Active ingredient synergy, dosage optimization, and clean-label solutions.
  • Regulatory & Safety Compliance Audit: Thorough review against UK Food Standards Agency (FSA) & European Food Safety Authority (EFSA) rules.
  • Health Claim Validation: Guidance on legally permitted health and nutrition claims for international markets.
  • Labelling & Technical Dossiers: Complete Finished Product Compliance Reports provided in PDF format for your quality audits.
  • Pre-Market Export Advice: Consultation on notification requirements across European and overseas destinations.
Comprehensive Capabilities

Our Core Product Development Solutions

From specialized active ingredient sourcing to final compliance sign-off, we manage every phase of your custom supplement journey under strict GMP controls.

01

Formula Development

Scientific ingredient blending, bioavailability planning, and galenic dosage selection across capsules, tablets, gummies, and powders.

02

Regulatory Audit

Rigorous pre-production checks for raw material safety, novel food status, upper nutrient limits, and allergen declarations.

03

Claim Strategy

Aligning product benefit statements with authorized health claims, enabling high-converting, fully compliant commercial marketing.

04

Compliance Report

Delivery of an extensive Finished Product Compliance Technical File (PDF) owned entirely by your company for registration and record-keeping.

Commercial Guidelines

Getting Started with Custom Manufacturing

To deliver uncompromising quality and focus our engineering resources effectively, Nutribl accepts custom New Product Development projects from established brands and serious market entrants.

If you are launching an entirely bespoke formula, our scientific team conducts dedicated trial runs, ingredient sourcing, and stability feasibility studies.

Development Fee & Order Guidance

  • NPD Fee: Standard bespoke formula development starts at £500 (incl. VAT) per SKU technical file.
  • Formula Ownership: All created formulations remain your brand's intellectual property.
  • Custom MOQs: Commercial minimum order quantities generally range from 60,000 to 100,000 capsules or tablets (or starting at 1,000 finished retail bottles depending on material specs and format).
  • Stock Formula Alternative: For low capital or immediate launch, explore our 120+ ready-to-ship stock range with MOQs from just 10 units.
Quality & Standards

Manufactured in the UK to Certified Global Standards

Every bespoke supplement batch engineered by Nutribl is produced in state-of-the-art facilities located in the United Kingdom.

We maintain full batch traceability, raw material Certificate of Analysis (COA) checks, and rigorous environmental controls so your products comfortably clear international customs and retailer audits.

BRCGS Global Food Safety Standard Certification

BRCGS Certified

Global Food Safety Standard accredited facility

GMP Standard Manufacturing Certification

GMP Standards

Strict Good Manufacturing Practice compliance

100% Quality Guarantee on UK Supplement Production

Quality Assured

Full batch traceability & lab testing

Structured Process

Our 4-Stage Product Development Lifecycle

01

Brief & Target Definition

We analyze your brand vision, target demographic, functional goals, and market pricing structure.

02

Engineering & Compliance

Formulators design the recipe, selecting high-potency ingredients while confirming regulatory compliance.

03

Technical Sign-Off

You receive the technical specification file, Finished Product Compliance Report, and lab sample validation.

04

Scaled UK Production

Upon approval, we move into commercial blending, encapsulation/tableting, packaging, and global dispatch.

Buyer Questions

Frequently Asked Questions on Custom Supplement Formulation

What is included in Nutribl's New Product Development (NPD) service?

Our comprehensive NPD service includes custom formula engineering, raw material stability assessment, regulatory compliance auditing, health claim validation, compliant labelling guidance, pre-market notification advice for international markets, and a full Finished Product Compliance Report provided as a master file.

What is the Minimum Order Quantity (MOQ) for custom formulations?

MOQs for bespoke custom products depend on active raw materials and dosage formats. Typical batch runs range between 60,000 to 100,000 capsules or tablets, or starting from 1,000 finished retail units depending on manufacturing constraints.

Are Nutribl formulations compliant with international export standards?

Yes. Every custom product is manufactured in the United Kingdom under BRCGS Global Standard and GMP accreditation. Our regulatory team reviews novel food status, permitted additive limits, and label declarations for compliance across the UK, EU, US FDA, Middle East, and Asia-Pacific markets.

Do I retain ownership of the developed supplement formulation?

Yes. Once the New Product Development process and compliance technical files are finalized, the formula remains your brand's intellectual property. There is no obligation to manufacture exclusively with Nutribl, though our clients typically proceed with us for seamless production.

How long does custom product development take from concept to batch delivery?

Formulation engineering and technical file generation usually take 2 to 4 weeks. Once artwork and raw materials are finalized, commercial batch manufacturing typically takes 4 to 6 weeks depending on component lead times.

Ready to Formulate Your Custom Supplement Range?

Speak directly with our UK regulatory and formulation specialists to discuss your custom project specifications, technical requirements, and target launch timelines.

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