What We Do

Services built around your product's success

One trusted partner across the entire cosmetic product lifecycle — manufacturing, testing, compliance and export readiness.

Contract Manufacturing

End-to-end manufacturing of skincare, haircare, body care and personal care products under your brand. From batch production to commercial scale, we ensure consistent quality at every run.

  • Skincare, haircare, body & personal care
  • Low MOQ to large-scale batches
  • Filling, packaging & labeling
Learn more about Contract Manufacturing

Product Development

Bespoke formulation and product innovation built around your brand promise and target consumer needs.

  • Brand brief to prototype
  • Sensory & performance tuning
  • Pilot batch evaluation
Learn more about Product Development

Stability Testing

Accelerated and real-time stability studies to determine shelf life, packaging compatibility and performance over time.

  • Accelerated & real-time studies
  • Temperature & humidity cycling
  • Shelf-life determination
Learn more about Stability Testing

Microbiology Testing

Comprehensive microbial quality and safety testing to international standards.

  • Total viable count
  • Pathogen screening
  • Preservative efficacy (challenge tests)
Learn more about Microbiology Testing

Product Information File (PIF)

Complete PIF preparation aligned with NAFDAC and international cosmetic regulations.

  • Safety assessment
  • Manufacturing & quality data
  • Labelling compliance
Learn more about Product Information File (PIF)

Regulatory Support

Hands-on support with NAFDAC product registration and international compliance requirements.

  • NAFDAC registration
  • International market dossiers
  • Audit readiness
Learn more about Regulatory Support

Export Readiness

Prepare your product and documentation for successful entry into ECOWAS, EU, US and Middle East markets.

  • Export-grade packaging & labelling
  • International compliance docs
  • Certificate of Free Sale support
Learn more about Export Readiness
How It Works

A clear path from brief to batch

Every service follows a transparent, milestone-driven process so you always know what comes next.

01 · Discover
02 · Define
03 · Develop
04 · Validate
05 · Deliver

Contract Manufacturing

  1. 1

    Brief & Scoping

    We capture your product vision, volumes, timelines and budget.

  2. 2

    Formulation Lock

    Your approved formula is transferred to our production team.

  3. 3

    Pilot Batch

    A trial batch is produced and signed off before scale-up.

  4. 4

    Full Production

    GMP-controlled mixing, filling, packaging and labeling.

  5. 5

    QC & Dispatch

    Every batch is QC-released and prepared for delivery.

Product Development

  1. 1

    Discovery Call

    We align on brand, consumer, claims and price point.

  2. 2

    Concept Brief

    Texture, fragrance, key actives and packaging direction agreed.

  3. 3

    Prototype Lab Work

    Formulators craft and iterate samples for your review.

  4. 4

    Sensory Tuning

    Refine feel, scent and performance until you sign off.

  5. 5

    Pilot Validation

    Pilot batch confirms scalability and stability.

Stability Testing

  1. 1

    Protocol Design

    Study plan built around your product and packaging.

  2. 2

    Sample Set-Up

    Units placed in controlled temperature and humidity chambers.

  3. 3

    Scheduled Pulls

    Samples tested at defined intervals over the study.

  4. 4

    Analytical Review

    Physical, chemical and sensory parameters tracked.

  5. 5

    Shelf-Life Report

    Final report with recommended shelf life and storage.

Microbiology Testing

  1. 1

    Sample Intake

    Samples logged in under chain-of-custody.

  2. 2

    Method Selection

    ISO-aligned methods chosen for the product matrix.

  3. 3

    Incubation

    Plates and broths held under controlled conditions.

  4. 4

    Enumeration & ID

    Counts taken and any pathogens identified.

  5. 5

    Certified Report

    Signed CoA issued with pass/fail against spec.

Product Information File (PIF)

  1. 1

    Data Gathering

    Formula, suppliers, specs and test data collected.

  2. 2

    Safety Assessment

    Toxicological review by qualified assessor.

  3. 3

    Label Compliance

    Artwork and claims reviewed against regulation.

  4. 4

    PIF Compilation

    Full dossier assembled in regulator-ready format.

  5. 5

    Ongoing Updates

    PIF kept live as formulas or claims evolve.

Regulatory Support

  1. 1

    Gap Assessment

    Current documentation reviewed against requirements.

  2. 2

    Dossier Build

    Application files prepared for target markets.

  3. 3

    Submission

    Filed with NAFDAC or international authorities.

  4. 4

    Queries & Response

    We handle agency questions on your behalf.

  5. 5

    Approval & Renewals

    Certificates issued; we track renewal dates.

Export Readiness

  1. 1

    Market Selection

    Target markets confirmed with their requirements.

  2. 2

    Compliance Mapping

    Formula and labels checked against each market.

  3. 3

    Documentation

    CoFS, CoA, MSDS and shipping docs prepared.

  4. 4

    Packaging Adaptation

    Artwork adapted to language and legal needs.

  5. 5

    Export Launch

    Goods cleared, shipped and ready for distribution.