We believe that the increased demand that would be borne out of increased aggregation, and evolving procurement models, by most African countries will create a gap that can only be met by companies who embrace technology, new manufacturing lines and better clean rooms.
As part of a comprehensive solution that CDI offers, we have relationship with companies that can, in a consultative way, map existing structures to desired structures while leveraging on cutting edge technologies, adhering to world class standards, and making sure local regulatory standards are met. We will hold your hands all the way.
These are lines that would help in Encapsulation and Tableting. Encapsulation and tableting, in pharmaceuticals, refers to different techniques to enclose medicines either in a relative stable shell known as capsules or as tablets. Many factors must be considered such as the fabrication of metals used, technology used, level of flexibility, level of versatility and maintenance.
Our relationships with global pharmaceutical manufacturing lines developers and our market insights means we can provide market driven guidance to the development, so that our application of truly tested capital budgeting techniques ensures true return on investment and value is not lost to shareholders.
Clean rooms are utilized as part of specialized industrial production including the manufacture of pharmaceutical items. They are designed to maintain extremely low levels of particulates such as dust, airborne organisms, or vapourised particles. Their cleanliness levels are typically quantified by the number of particles per cubic meter at a predetermined molecule measure.
Technological advancements have made this an art and it takes partnership with the right companies to get the best of the technological suite needed to achieve scale.
Our relationships with global clean room developers and our market insights means we can provide market driven guidance to the development, so that our application of truly tested capital budgeting techniques ensures true return on investment and value is not lost to shareholders.
Building Plants to Good Manufacturing Practice (GMP) guidelines
Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.
We have the relationships with most regulatory bodies on the continent and the global purchasers hence we can help with the financial models to justify the extra investment.