Home > Super Generic APIs > Formulation Optimization
Formulation Optimization
Abiozen’s formulation optimization capabilities are designed to elevate the therapeutic value of our super generic APIs through enhanced bioavailability, stability, and patient-focused delivery systems. Our formulation experts utilize a range of advanced technologies to engineer solutions tailored to diverse clinical needs, ensuring regulatory compliance and commercial readiness from development to deployment.
Solubility Enhancement
To address one of the most common barriers in drug performance, we apply state-of-the-art techniques such as hot-melt extrusion, solid dispersion, and nanoparticle engineering to improve solubility and absorption profiles. Inspired by Thermo Fisher Patheon’s leading-edge formulation methodologies, our solubility optimization enhances the bioavailability of poorly water-soluble compounds and supports more effective therapeutic delivery.
Controlled-Release Mechanisms
We develop sophisticated controlled-release systems that ensure a consistent release of the active ingredient over time, reducing dosing frequency and improving patient adherence. Leveraging Curia Global’s innovation frameworks, these targeted and sustained-release formulations are customized for therapeutic precision, clinical efficacy, and commercial differentiation.
Injectable Formulations
Our formulation scientists specialize in parenteral delivery formats including sterile liquids and lyophilized powders. These injectable formulations are optimized to meet complex clinical requirements and regulatory expectations for safety, stability, and sterility. Following a model inspired by Thermo Fisher CRDMO, we integrate process efficiency with compliance rigor to support seamless transition from development to manufacturing.
Therapeutic Performance, Delivered Efficiently
By aligning innovation with regulatory strategy, Abiozen ensures that each formulation not only meets technical specifications but also delivers high therapeutic impact with minimized development timelines. Our integrated formulation optimization services support faster time-to-market and greater commercial success for super generic API products worldwide.
Connect with Abiozen
We thrive on tackling complex challenges—and we’d love to learn about yours. Reach out to explore how we can support your program’s unique requirements.
Related Resources

IP Management and Global Regulatory Support: Comprehensive intellectual property and compliance solutions for seamless market entry
property and compliance solutions for seamless market entry processes for superior purity and stability. global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste

Advanced Crystallization and Purification Techniques: Cutting-edge processes for superior purity and stability.
processes for superior purity and stability. global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste management systems to uphold safety and environmental standards.

High-Volume API Synthesis: Precision-driven, scalable production to meet global demand
global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste management systems to uphold safety and environmental standards. real-time environmental monitoring to guarantee sterility.

IP Management and Global Regulatory Support: Comprehensive intellectual property and compliance solutions for seamless market entry
property and compliance solutions for seamless market entry processes for superior purity and stability. global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste

Advanced Crystallization and Purification Techniques: Cutting-edge processes for superior purity and stability.
processes for superior purity and stability. global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste management systems to uphold safety and environmental standards.

IP Management and Global Regulatory Support: Comprehensive intellectual property and compliance solutions for seamless market entry
property and compliance solutions for seamless market entry processes for superior purity and stability. global demand. absence of microbial contamination, essential for injectable products compliance with ICH Q3C guidelines, ensuring safety and purity residual moisture levels below 1%, critical for long-term stability. for HPAPIs, equipped with decontamination protocols and waste