High-throughput natural metabolite screening, target engagement validation, chromatographic fingerprinting, and turnkey cGMP manufacturing tailored for France’s dermo-cosmetic, nutricosmetic, and botanical drug sectors.
Accelerating phytochemical qualification through high-resolution analytical separation, orthogonal mass spectrometry, and verified clinical phase transitions.
France serves as the global epicenter for haute-cosmetics, phytotherapy, and high-standard nutricosmetics. Meeting local compliance and efficacy expectations demands precision screening technologies.
France’s Cosmetic Valley and pharmaceutical hubs in Lyon and Paris set the worldwide standard for skin barrier restoration, anti-senescence, and microbiome-friendly compounds. Screened actives must provide mechanistic proof at cellular and genetic pathways.
The French Agence Nationale de Sécurité du Médicament (ANSM) and DGCCRF enforce strict contaminant restrictions, including thresholds for polycyclic aromatic hydrocarbons (PAHs), heavy metals, ethylene oxide, and over 500 pesticide residues.
Industrial buyers across Grasse, Nouvelle-Aquitaine, and Brittany require solventless supercritical CO2, subcritical water extraction, or bio-fermented fractions that align with ISO 16128 naturality index scores and avoid persistent petrochemical solvents.
Bridging empirical botanical knowledge with quantitative chemistry. Our platform delivers high-yield separation, metabolomics identification, and turn-key scale-up under one roof.
Phenotypic and target-directed multi-well platforms scanning antioxidant capacities (ORAC, DPPH), anti-inflammatory cytokine modulation (TNF-α, IL-6), elastase/collagenase inhibition, and mitochondrial energy enhancement.
UPLC-QTOF-MS/MS coupled with chemometric profiling quickly eliminates known baseline compounds, isolating novel functional fractions and defining comprehensive European Pharmacopoeia (Ph. Eur.) HPTLC chemical profiles.
From pilot multi-kilogram test batches to multi-metric-ton supply. We provide end-to-end spray drying, crystallization, encapsulation, and packaging across cleanroom facilities meeting ISO 22716 and EU-GMP Grade D qualifications.
Seamless supply chain integration supported by complete technical files directly compliant with EU Regulation (EC) No 1223/2009 for cosmetics and EFSA frameworks for dietary nutrition.
Complete safety assessments including raw material characterization, toxicological profile (NOAEL, MoS calculation), absence of CMR substances, and challenge test analytics verified by EU qualified safety assessors (Eurofins-ready).
Evaluating plant extracts against EU Regulation 2015/2283. Distinguishing between traditional herbal registration pathways (THMPD) and novel status to bypass clinical authorization roadblocks.
Full compliance with the French Biodiversity Law (Loi Biodiversité). Complete botanical supply chain tracking from sustainable cultivation plots, guaranteeing Prior Informed Consent (PIC) and Mutually Agreed Terms (MAT).
Connect with our senior analytical chemists and regulatory strategists to commission high-yield botanical screening or analytical method validation.
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Simulating ligand-protein binding affinity across thousands of phytochemical secondary metabolites against human epigenetic targets before wet lab assaying, reducing discovery cycles from 18 months to 4 weeks.
Utilizing engineered probiotic fermentation to convert bulky, low-bioavailability saponins and polyphenols into aglycone formats with 10x higher cutaneous absorption and enhanced oral metabolic activity.
Developing advanced circular economy streams that screen and isolate potent flavonoids, polyphenols, and pectin oligosaccharides from French agro-food co-products (grape pomace, prune kernel, olive mill residue).
Addressing the operational, analytical, and intellectual property queries standard to European contracting partnerships.
Explore our complete range of certified botanical research capabilities, potency profiling, in vitro bio-screening, and contract manufacturing solutions.
