galenIQ™ Redefines the Indian Excipient Market Through Innovation, Education, and
Real-World Performance
India | Pharmaceutical Excipients | Oral Solid Dosage Innovation
India's pharmaceutical excipient landscape is undergoing a gradual but significant
transformation, driven by the growing need for high-performance, formulation-ready
materials. In a recent episode of Excipient Talk, Michael Black, Senior Sales
Manager for galenIQ™, discussed this evolution with Siddhant Waikar, Business
Development Manager at SFA Food and Pharma Ingredients, highlighting the journey of
introducing galenIQ™ to the Indian pharmaceutical market.
With SFA Food and Pharma Ingredients marking 25 years of operations and maintaining
a long-standing partnership with Beneo, the discussion shed light on the strategic,
technical, and educational efforts required to establish a novel excipient in one of
the world's most competitive generics-driven markets.
Addressing the Challenges of India's Generics-Focused Pharma Industry
India's pharmaceutical industry is largely dominated by generic drug manufacturing,
where formulations are often benchmarked against Reference Listed Drugs (RLDs) from
Europe and the United States. This environment naturally creates resistance to
replacing established excipients with newer alternatives.
According to Siddhant Waikar, galenIQ™ also faces the common challenge of being
grouped alongside traditional polyols such as mannitol and sorbitol—materials that
have been industry standards for decades. However, galenIQ™ differentiates itself
through its unique physicochemical properties, particularly in flowability,
compressibility, and stability.
To overcome initial barriers, SFA has adopted a sensory-first, application-driven
approach. Through blind taste kits, formulation prototypes, and direct technical
engagement, customers are able to experience the material's flow, whiteness, and
rapid dissolution kinetics firsthand. These evaluations frequently serve as a
catalyst for deeper technical discussions on performance advantages in oral solid
dosage formulations.
Demonstrated Success Across Therapeutic Applications
The growing acceptance of galenIQ™ in India is supported by tangible, real-world
formulation success:
Anti-malarial tablet stability: In one significant case, two grades of
galenIQ™ were used for granulation and extra-granular compression in an
anti-malarial tablet. The excipient played a critical role in maintaining shelf-life
stability under high-temperature and high-humidity conditions in West Africa,
supporting the product's suitability for global health programs.
Caffeine tablet reformulation: In another instance, galenIQ™ replaced
sorbitol in a caffeine tablet formulation. Due to its lower hygroscopicity, the
switch resulted in reduced moisture uptake and improved weight stability, leading to
rapid customer approval following trial evaluation.
Building the Future of Excipients Through Education and Market Impact
Looking ahead, the long-term vision for galenIQ™ in India is to become a widely
recognized, mainstream excipient across pharmaceutical product labels. Given India's
position as a global pharmaceutical manufacturing hub, increased adoption within the
country has the potential to influence formulation practices worldwide.
A key focus area remains technical education. The galenIQ™ and SFA teams are
actively working to ensure the excipient is included in academic literature,
formulation references, and training programs for future scientists, PhD
researchers, and formulation experts.
These initiatives will be further showcased at CPHI India (25–27 November), along
with a dedicated technical seminar in Baddi, widely regarded as Asia's largest
pharmaceutical manufacturing hub.
About galenIQ™
galenIQ™ is a multifunctional isomalt-based pharmaceutical excipient designed for
oral solid dosage forms, offering excellent flowability, compressibility, low
hygroscopicity, and stability under challenging climatic conditions.