Services
Explore our specialized services for dietary supplement research, development, and formulation.
We commit to providing innovative solutions and supporting you throughout the production process. As your trusted partner, we assist in creating essential formulas and developing high-quality products.
Whether entering product development or enhancing existing formulations, we are here to provide the necessary support and guidance for success in the ongoing evolution of dietary supplement production.
Preformulation and Theoretical Formulation
Preformulation studies are an essential component of the drug development process and provide the scientific basis for formulation development. It provides the physical, chemical and mechanical properties of a new drug and helps us choose the ingredients (excipients) that should be used in the preparation.
Preformulation studies can be classified into several aspects. First, the characterization of the fundamental properties. This includes understanding solubility in different solvents, permeability, stability in solid state, stability in solution state etc. Second, we understand the derived properties of the preformulation, such as morphology, particle size, bulk density, etc. The last activity carried out within the preformulation studies is represented by compatibility studies with excipients, to investigate the stability of the active substance molecule in the presence of excipients as well as compressibility, encapsulation, etc. properties.
Product Development and Production File Preparation
This stage is an important one and involves the initiation of tests to evaluate the feasibility of the theoretical formula on a laboratory scale. Adjustments to the formula can be made if necessary to improve patient compliance. Suppinno develops the complete and well-documented dossier, which reflects every stage of the production process, to ensure the success and quality of the product on an industrial scale.
Quality Control
The Quality Control activity is carried out to the standards required by the Rules of Good Manufacturing Practice and the Rules of Good Laboratory Practice.
Suppinno makes available the physico-chemical and microbiological analyzes for testing the quality of the finished product and takes care of obtaining the analysis bulletin of the finished product necessary for its registration with the regulatory authorities in the field.
Preparation and Submission of Pharmaceutical Files
Suppinno can provide assistance to its partners in the process of drawing up and submitting files in order to obtain the notification of pharmaceutical products. We ensure that responses to the deficiency letters of all competent authorities are submitted as soon as possible and we make available to the authorities all data relating to the safety, efficacy and quality of the product.
Consultancy in the Relationship with the Authorities
We offer professional consultations to all partners who request them.
We provide our partners with support regarding the preparation of documentation for authorizations, approvals, notifications, as well as specialized help in various situations related to relations with the authorities, which may arise after the submission of the file.
Technological Transfer
We provide specialized support and physical assistance for industrial-scale transfer to the partner's chosen production site for product launch.
Online presence
To successfully complete the pharmaceutical product development and presentation process, we recognize the vital importance of an effective online presence. So we also focus on creating websites that highlight the scientific excellence of each project, providing an optimal digital platform for clearly communicating the benefits of these products. No matter what stage you are at, we can offer customized website development solutions, combining attractive design with tailored functionality to help build an outstanding online presence for your innovative projects developed in collaboration with us and beyond.