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Filos Biopharma offers comprehensive pharmaceutical services to global companies, including formulation development, regulatory consulting, clinical trial management, and strategic lifecycle optimization for market success.

What We Can Do for You

Forward Integration for API Companies

We help API manufacturers expand into finished dosage formulations, enhancing market presence and profitability.

Backward Integration for FP Companies

We assist finished dosage form (FP) companies in securing API sources, ensuring supply chain efficiency and cost control.

Infrastructure Development

We support pharmaceutical companies in scaling operations with optimized manpower, advanced machinery, and cutting-edge technology.

Quality by Design (QbD) Implementation

Our QbD expertise ensures systematic pharmaceutical development, improving product quality, consistency, and regulatory compliance.

Advanced Formulation Development

We specialize in Galenical/lab-scale formulation of oral, topical, and injectable products for various therapeutic needs.

NCE Formulation Development

Our team develops novel drug formulations (NCEs) to enhance drug efficacy, stability, and market differentiation.

Bioavailability Enhancement

We optimize API formulations to improve bioavailability, ensuring better drug absorption and therapeutic performance.

Formulation Upgradation

We enhance existing formulations for better efficacy, patient compliance, and regulatory approval.

Seamless Technology Transfer

Our technology transfer services ensure smooth transition from development to commercial-scale production.

New Dosage Form Innovations

We develop novel dosage forms tailored to improve patient adherence and therapeutic outcomes.

New Drug Combinations

We create innovative drug combinations for enhanced efficacy and competitive market positioning.

New Drug Applications (NDAs)

Our regulatory team provides end-to-end support for successful NDA submissions and approvals.

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