PHARMACEUTICAL

Pharmaceutical Market: a sector where taste drives treatment adherence

The pharmaceutical flavouring market is experiencing steady growth, driven by increasing demand for more acceptable and better-tolerated formulations.

Today, flavouring has become a key strategic tool for improving medicine acceptability, particularly for oral dosage forms (syrups, solutions, powders, chewable tablets, etc.).

Scientific data confirms that taste is no longer a secondary consideration, but a key parameter in pharmaceutical development.

A study by the European Society of Medicine highlights that 65% of active pharmaceutical ingredients (APIs) exhibit bitterness, requiring dedicated taste-masking strategies. It also shows that most APIs present multiple aversive attributes (off-notes, unpleasant smells, irritation), increasing the sensory complexity of oral formulations.

At a global level, several analyses confirm that pharmaceutical flavourings represent a multi-billion-dollar market, driven by rising expectations for palatability, particularly in paediatric and OTC formulations. Most studies indicate annual growth rates between 4% and 7%, reflecting sustained and long-term momentum.

Taste has become a decisive factor in therapeutic effectiveness and the commercial success of oral dosage forms.

A HIGHLY DEMANDING MARKET WITH SPECIFIC CONSTRAINTS

The pharmaceutical sector is characterised by unique requirements:

STRICT REGULATORY CONSTRAINTS

legal naming, EU and international compliance, usage restrictions

HIGH QUALITY REQUIREMENTS

Certificates of Analysis (CoA), specifications, traceability, batch compliance

PROCESS AND DOSAGE FORM CONSTRAINTS

solubility, stability, API interactions, manufacturing conditions

HIGH SENSORY REQUIREMENTS

bitterness, off-notes, flavour consistency over time

DIVERSE INTERNAL STAKEHOLDERS

R&D, Quality, Regulatory Affairs, Procurement

This market requires a partner capable of combining rigour, robust documentation, strong sensory performance and deep understanding of industrial constraints.

HOW WE SUPPORT PHARMACEUTICAL STAKEHOLDERS

Syrups, solutions, powders, ODTs, chewable and effervescent tablets, gummies…

Liquids, powders, encapsulated/microencapsulated formats, granules.

CoA, specifications, legal naming, usage restrictions, EU and international compliance.

A single point of contact to streamline collaboration between R&D, Quality, Procurement and Regulatory Affairs.

A RELIABLE PARTNER FOR YOUR DEMANDING PHARMACEUTICAL DEVELOPMENT PROJECTS

Our flavour solutions are developed with a certified French manufacturer, in full compliance with pharmaceutical industry requirements, ensuring:

CONSISTENT QUALITY FROM BATCH TO BATCH

FULL TRACEABILITY OF RAW MATERIALS AND MANUFACTURING PROCESSES

DOCUMENTATION ALIGNED WITH QUALITY AND REGULATORY EXPECTATIONS

RECOGNIZED EXPERTISE DEDICATED TO PHARMACEUTICAL FORMULATIONS

DEVELOPING A PHARMACEUTICAL FORMULATION?

Let’s discuss your project, describe your needs and speak with an expert.