Curtis Health Caps
Contract Development and Manufacturing Services for Pharmaceutical Projects
Curtis Health Caps provides soft gelatin capsules, non-sterile liquid products, and research and development (R&D) services for the pharmaceutical sector.
Curtis Health Caps is a multinational contract development and manufacturing organisation (CDMO) specialising in soft gelatin capsules, non-sterile liquid products, and research and development (R&D) services.
We offer a comprehensive range of solutions, from R&D services and regulatory audits to quality consultancy, production, storage and transport, all carefully tailored to the ever-changing needs of the market. Our services are in high demand from pharmaceutical contract manufacturing companies.
We operate a modern and innovative machinery park in Poland that features a well-equipped R&D department, employing experts across a range of fields.
Professional support for pharmaceutical product development
As a CDMO, Curtis Health Caps provides clients with high-quality service throughout the whole product development process, from initial concept to final product.
Our experienced team can offer professional support with formulation and choosing the most suitable packaging. This allows you to easily add to your portfolio and find new pharmaceutical products for in-licensing.
Other services we offer include portfolio analysis, product licensing, dossier audits and regulatory support.
Soft gelatin capsule development to client specifications
As part of the contractual production of medicinal products and food supplements, Curtis Health Caps allows clients to individually select the colour and shape of soft capsules to suit their specific requirements and preferences.
Soft gelatin capsules allow active pharmaceutical ingredients (APIs) to be absorbed quickly, with the gelatin shell guaranteeing airtight packaging for the ingredients in the capsule fill and protecting them against the effects of external factors.
The encapsulation process’ specificity ensures the product keeps its microbiological safety without the use of preservatives, which is particularly important in products intended for children. In addition, the capsule shell is made from biodegradable and environmentally friendly components.
Development of pharmaceutical products in non-sterile liquid forms
Curtis Health Caps specialises in contract manufacturing medicinal products, food supplements and medical devices, as well as liquid forms of syrups, suspensions, drops and sprays. We can manufacture non-sterile liquid syrups, suspensions, drops or sprays according to clients’ preferences and customer needs.
Liquid-form products offer a wide dosage spectrum and have high absorption rates. They do not pose a risk of choking and are easier to swallow, making them more suitable to administer to children and elderly patients.
Our reliable personnel and technological resources ensure the quality of our services.
Research and development services for pharmaceutical projects
Curtis Health Caps provides R&D services at all stages of development for capsules and non-sterile liquid products, from initial concept to finished product.
We help clients develop new product formulations to match market trends and consumer needs, as well as offering assistance for the development and modification of existing products. Our team can also carry out microbiological tests of raw materials and medicinal products in-line with pharmaceutical requirements.
Our R&D experts can assist with the development and validation of analytical methods for products; the development, validation or implementation of analytical methods for raw materials; and the optimisation of analytical procedures.
All these works are conducted according to International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, pharmacopoeial requirements, and good manufacturing practice (GMP) standards.
Manufacturing technology for pharmaceutical products
Curtis Health Caps offers a wide range of services for manufacturing soft gelatin capsules and non-sterile liquid forms. These include developing formulations for new products based on the latest market trends and literature, modifying existing product formulations, selecting raw materials of adequate quality from certified suppliers, and developing technology for trial and pilot batches.
Regulatory compliance checks for product development
Curtis Health Caps provides regulatory audits for a range of medicinal products and medical devices.
We can assess products, devices and API manufacturing sites for compliance with different standards, including GMP and International Organisation for Standardisation (ISO) requirements. We also offer GMP services and training.
Our manufacturing facility in Przeźmierowo, Poland, is certified as complying with the EU’s GMP standards and the eighth edition of the UK’s Brand Reputation Compliance (BRC) Global Standards. We also hold ISO 9001:2015, 14001:2015 and 13485:2016 certifications.