Three sectors. One standard. Operating in 14 countries.
4CF Group · est. 2007 Manufacturing · Consulting · Ingredients

One partner,
three capabilities —
built around your product.

4CF Group brings manufacturing, regulatory and ingredient capability under one roof. We help brands and developers in pharma, cosmetic and food turn formulations into compliant, shippable products — anywhere in the world.

3
Sectors under one group
14
Countries served
19yrs
Operating since 2007
4CF · GROUP / CAPABILITY MAP
REV · 26.04
THREE INTERSECTING DOMAINS
01 · Manufacturing
02 · Consulting
03 · Ingredients
3 sectors
Seoul · Suwon Tokyo · Osaka Shanghai · Suzhou Frankfurt · Basel Boston · Cambridge São Paulo · Mexico City est. 2007 ISO 13485 · cGMP · HACCP
02 — Sectors

Three businesses that compound when bought from one partner.

01
01 / Manufacturing

ODM & OEM — built thin, built fast.

Contract manufacturing of oral dissolved films and adjacent dosage formats, with in-house formulation R&D.

Oral dissolved films Strip & patch formats Formulation R&D Pilot & commercial scale Serialised packaging
Explore manufacturing
SUWON · LINE 02ODF / 38μm
02
02 / Consulting

GMP & Regulatory — cleared for every market.

GMP audits, ISO certification, medical device CE/FDA submissions, food, cosmetic & pharma RA / QA.

ISO 9001 · 13485 · 22000 cGMP audit & remediation Medical device CE / FDA 510(k) Cosmetic CPSR / PIF Food & supplement filings GlobalRegAI integrated
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EU · GMP DOSSIERANNEX 13
03
03 / Ingredients

Specialty ingredients — sourced, refined, supplied.

Sourcing, trading and co-development of specialty ingredients across nutrition, cosmetic, pharmaceutical and industrial applications.

Nutrition & functional Cosmetic actives API & excipients Industrial specialty Co-development & co-pub
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NUTRITION · LOT 4087COA · ATTACHED
03 — How we work

Customer-led innovation, end-to-end. We don't sell stages — we deliver outcomes.

STEP / 01
Brief & need
A direct conversation with our R&D and regulatory leads — not a sales script. We identify the molecule, the market, and the constraint.
STEP / 02
Feasibility
Formulation screen, regulatory pathway map and ingredient sourcing options delivered as a single feasibility report in 10 working days.
STEP / 03
Develop
Pilot batches, analytical method development, stability studies and the regulatory dossier built in parallel — not in series.
STEP / 04
Manufacture
Captive lines in Korea and contract partners across APAC and EU. Flexible batch sizes from 50k to 100M units per year, fully serialised.
STEP / 05
Supply & sustain
Direct distribution, post-market surveillance, variation management and lifecycle support — held together by one account team.

Sized for serious work, structured for speed.

04 — By the numbers
2B
Films & units produced annually across captive and partner lines.
Capacity
340+
Active customer accounts across pharma, cosmetic and food.
Customers
1,400+
Specialty ingredients traded across four categories.
Catalogue
22
Regulatory authorities engaged across EU, APAC and the Americas.
Reach
0
Critical findings in routine inspections since 2018.
Quality
96%
Customer retention beyond five years on the active programs.
Retention
Figures aggregated FY23–FY25 across the three sectors. Audited summary on request.
Certifications & standards
EU GMP
US FDA
PMDA
MFDS
NMPA
ISO 13485
ISO 22000
HACCP