{"id":1073,"date":"2026-07-15T16:38:41","date_gmt":"2026-07-15T14:38:41","guid":{"rendered":"https:\/\/www.pharmarome.fr\/rd\/"},"modified":"2026-07-23T15:52:45","modified_gmt":"2026-07-23T13:52:45","slug":"rd","status":"publish","type":"page","link":"https:\/\/www.pharmarome.fr\/en\/rd\/","title":{"rendered":"R&D"},"content":{"rendered":"

R&D<\/h1>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

R&D: Secure your product development and enhance sensory performance<\/h2>\n<\/div><\/div><\/div><\/div><\/div>
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An unsuitable flavouring can compromise stability, complicate the process and extend your development cycles. We help you select a solution that is compatible, robust and high-performing from the laboratory stage.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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YOUR R&D CHALLENGES<\/h2>\n<\/div><\/div><\/div><\/div><\/div>
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INCOMPATIBILITY WITH YOUR DOSAGE FORM OR PROCESS (CARRIER, SOLUBILITY, PROCESSING CONDITIONS)<\/h3><\/div><\/div><\/div><\/div>
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EMERGENCE OF BITTERNESS, EXCESSIVE ACIDITY OR OFF-NOTES LINKED TO ACTIVE INGREDIENTS<\/h3><\/div><\/div><\/div><\/div>
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INSTABILITY OVER TIME OR LACK OF REPRODUCIBILITY<\/h3><\/div><\/div><\/div><\/div><\/div>
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INAPPROPRIATE FORMAT SELECTION (LIQUID, POWDER, ENCAPSULATED\/MICROENCAPSULATED)<\/h3><\/div><\/div><\/div><\/div>
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LENGTHY TESTING CYCLES AND COSTLY ITERATIONS<\/h3><\/div><\/div><\/div><\/div>
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PATIENT ACCEPTABILITY AND ADHERENCE<\/h3><\/div><\/div><\/div><\/div><\/div>
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These challenges are common across R&D teams in pharmaceutical, nutraceutical and CMO\/CDMO environments\u2026<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/section>

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OUR ROLE: ENSURE THE RELIABILITY OF YOUR DEVELOPMENT PROJECTS<\/h2>\n<\/div><\/div><\/div><\/div><\/div>
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For over 50 years, we have supported R&D teams in selecting flavour solutions aligned with their formulation constraints, processing conditions and sensory performance objectives.<\/p>\n

Practical support at every stage:<\/p>\n<\/div><\/div><\/div><\/div><\/div>

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1. FORMAT SELECTION<\/h3>\n<\/div><\/div>
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We define the optimal solution based on your application: liquid flavour, spray-dried powder, granule, or encapsulated\/microencapsulated format.<\/p>\n<\/div><\/div><\/div><\/div>

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2. SENSORY OPTIMISATION<\/h3>\n<\/div><\/div>
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We work on flavour profile, bitterness masking, off-note control, overall taste balance and long-term sensory consistency. We refine the flavour profile until it meets your objectives and supports improved treatment adherence.<\/p>\n<\/div><\/div><\/div><\/div><\/div>

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3. VALIDATION TESTING<\/h3>\n<\/div><\/div>
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Organoleptic and physicochemical evaluation, with dosage optimisation based on your data.<\/p>\n<\/div><\/div><\/div><\/div>

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4. PREPARATION FOR INDUSTRIAL SCALE-UP<\/h3>\n<\/div><\/div>
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What works at laboratory scale must perform at industrial scale. We assess formulation robustness against process variations (temperature, shear, humidity, mixing time).<\/p>\n<\/div><\/div><\/div><\/div><\/div>

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5. FLAVOUR MATCHING<\/h3>\n<\/div><\/div>
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If your existing formulation must evolve (regulatory update), be standardised or replaced, we analyse the initial sensory profile and propose a 100% compliant<\/strong> alternative, supported by a comparative technical and sensory report.<\/p>\n<\/div><\/div><\/div><\/div>

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KEY TOPICS WE COVER WITH R&D TEAMS<\/h2>\n<\/div><\/div><\/div><\/div><\/div>
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