Hands-on from regulatory submissions and scientific documentation to quality systems, risk assessments and lifecycle management.across EU, FDA and international markets.
Claims, labelling and documentation issues rarely become visible until products reach the market.
Early identification of compliance gaps helps avoid corrective actions, relabelling requirements and unnecessary delays.
Hands-on support across cosmetic regulatory and compliance activities.
Product Information & Documentation
→ Product Information Files (PIF)
→ PIF reviews
→ Documentation updates
→ Technical documentation maintenance
→ Traceability documentation
Claims & Product Positioning
→ Claims substantiation reviews
→ Marketing claims assessments
→ Communication compliance reviews
→ Product positioning assessments
→ Risk evaluation of claims
Regulatory Compliance
→ CPNP notifications
→ Regulatory reviews
→ Compliance assessments
→ International regulatory support
→ Market access documentation
Responsible Person Support
→ Responsible Person activities
→ Compliance oversight
→ Regulatory coordination
→ Documentation maintenance
→ Market surveillance support
Quality & Manufacturing
→ Quality Assurance Systems (QAS)
→ Supplier qualification
→ GMP support
→ Manufacturing documentation
→ Traceability reviews
Product Lifecycle Support
→ Formula modifications
→ Reformulation assessments
→ Documentation updates
→ Market expansion support
→ Regulatory maintenance
These examples represent only a selection of the activities we support. If your requirement is not listed, contact us to discuss your specific needs.
Confidential discussion. No commitment. Practical guidance from day one
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