DRUG FORMULATION
At Pharma FSL, we offer specialized Drug Formulation Services designed to transform innovative research into effective, safe, and market-ready pharmaceutical products. Our expert team works closely with clients to develop customized formulations that meet regulatory standards and therapeutic goals, whether for oral, topical, injectable, or controlled-release delivery systems.
Using state-of-the-art technology and rigorous scientific methodologies,
we support every stage of the formulation process—from pre-formulation
studies and excipient selection to stability testing and scale-up. Our
focus is on optimizing bioavailability, patient compliance, and product
shelf life while ensuring cost-effectiveness. Whether you're a biotech
startup or an established pharmaceutical company, Pharma FSL is your trusted
partner for reliable, efficient, and high-quality drug formulation solutions.
At PHARMA FSL, our Drug Formulation
Services are at the heart of our pharmaceutical innovation. We specialize in
transforming active pharmaceutical ingredients (APIs) into safe, effective, and
patient-friendly medications. With a team of experienced formulation scientists
and access to world-class facilities, we offer comprehensive formulation solutions
for a wide range of dosage forms.
Our Capabilities Include:
- Pre-formulation Studies
Detailed physicochemical analysis of APIs to determine solubility, stability, and compatibility with excipients—ensuring a solid foundation for product development. - Formulation Development
Customized formulation strategies for oral solids (tablets, capsules), liquids, topical creams, injectables, and advanced drug delivery systems such as sustained-release and targeted-release formulations. - Process Development & Optimization
Designing scalable and cost-effective manufacturing processes using Quality by Design (QbD) principles to ensure consistent product quality and performance. - Analytical Testing & Validation
Rigorous in-house testing including dissolution, stability, and bioavailability assessments to support regulatory submissions and ensure product efficacy and safety. - Clinical Trial Supply
Formulating and supplying investigational medicinal products (IMPs) for use in clinical studies, aligned with global GMP standards. - Regulatory Support
Providing technical documentation and regulatory support for formulation dossiers and product registration in local and international markets.