DRUG FORMULATION
At EDBIO Pharm, 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, EDBIO Pharm is your trusted
partner for reliable, efficient, and high-quality drug formulation solutions.
At EDBIO Pharm – Edinburgh Pharmaceutical Industries Limited, 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.