Oral Solid Dosage
Formulation Development
Our Oral Solid Dosage Formulation Services provide end-to-end development support for tablets, capsules, and
oral films across multiple therapeutic segments.
We apply an integrated formulation approach to support efficient progression from early development through clinical
and commercial readiness.
Oral Solid Dosage Development Overview
Oral solid dosage forms remain one of the most widely utilized pharmaceutical product categories due to their convenience, dosing accuracy, and manufacturing flexibility.
Our formulation development approach integrates pre-formulation data, biopharmaceutics, process development, and analytical support to enable robust and scalable oral solid dosage products.
We support a wide range of product designs, including immediate-release, modified-release, and patient-centric oral solid forms.
NCE Clinical Formulation Development
We provide comprehensive formulation development support for Phase I, II, and III clinical trials involving new chemical entities.
Oral solid formulations are designed to meet performance, manufacturability, and regulatory requirements that support smooth clinical progression.
ORAL SOLID DOSAGE EXPERTISE
Tablet
Formulations
Development of immediate-release, controlled-release, and modified-release tablets guided by biopharmaceutics, excipient selection, and manufacturability.
Capsule
Dosage Forms
Development of hard gelatin and HPMC capsules, including powder-filled, pellet-based, and liquid-filled systems designed for consistent performance.
Oral
Films
Development of fast-dissolving and buccal oral films focused on patient convenience, dose accuracy, uniform drug distribution, and formulation stability
Differentiated Generic & OTC Product Development
We support the development of differentiated generic and over-the-counter oral solid dosage products through structured formulation and process development activities.
Our approach focuses on creating formulations that enhance performance, patient compliance, and lifecycle value.
- Concept ideation and formulation strategy
- Proof-of-concept and in-vitro evaluation
- Process and analytical method development
- Packaging, stability, and technology transfer support
Quality, Compliance & Development Alignment
Oral solid formulation development activities are conducted within structured quality systems to ensure data integrity, traceability, and alignment with regulatory expectations.
- Documented formulation and process development
- Integrated analytical and stability support
- Regulatory-ready development documentation
- Alignment with scale-up and manufacturing needs
Why Oral Solid Dosage Matters
Oral solid dosage forms offer flexibility, patient convenience, and compatibility with large-scale manufacturing.
- Predictable drug release and absorption
- Improved patient adherence
- Scalable and cost-effective manufacturing
- Support for regulatory submissions and lifecycle management
Looking for a Trusted Pharmaceutical Partner?
Let’s discuss how our pharmaceutical capabilities can support your requirements.