Formulation Development

FORMULATION DEVELOPMENT

Mastering Innovation for Superior Therapeutics

Formulation development is the intricate process of designing and refining pharmaceutical products to ensure optimal efficacy, safety, and patient experience. At Remik, we specialise in this field by being a strategic partner in your growth, leveraging external expertise and resources to drive innovation. Our lean organisational structure makes sure we remain agile and efficient, delivering high-quality formulations that meet the highest industry standards while adapting to evolving market needs.

  1. Strategic Direction: We establish a strategic direction by pinpointing therapeutic areas or specific drug types where new formulations or enhancements to existing ones are needed, ensuring we address critical gaps and advance pharmaceutical innovation.

  2. In-house Expertise: Our team of experts is at the core of pioneering everything we do at Remik. From making advances in pharmaceutical sciences and formulation chemistry to overseeing project management and quality assurance, we have the team and resources that underline success.

  3. Partnerships with Formulation Experts: To develop and innovate formulations, Remik Pharma has strategic partnerships with contract development and manufacturing organisations (CDMOs), formulation development laboratories, and academic institutions with expertise in pharmaceutical formulation. We work closely with them on pre-formulation, formulation design, prototype development, optimisation studies, and stability testing.

  4. Regulatory Compliance: At Remik Pharma, our robust systems and processes ensure that all formulation development activities adhere to regulatory guidelines and requirements. This includes documentation, data management, compliance with Good Manufacturing Practices (GMP) and other relevant standards.

  5. Intellectual Property Management: Throughout the formulation development process, we manage intellectual property (IP) considerations, such as patent filings and protection of proprietary formulations and technologies.

  6. Commercialisation Planning: After a formulation is successfully developed and optimised, we move into commercialisation planning. This phase may involve partnering with major pharmaceutical companies for advanced development, negotiating licensing agreements, or pursuing independent routes to bring the innovation to market.