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Customized solutions from formulation to final packaging
Secondary pharmaceutical manufacturing typically includes the final formulation, so the need to meet current Good Manufacturing Practice (cGMP) regulations and quality standards are paramount.
Conventional methodology uses a series of clean rooms which incurs significant construction and operational costs and handling new, highly toxic powders may be problematical.
Alternatively, with careful thought and design, all areas of the plant can be contained by interfacing the processes in semi-continuous design and guaranteeing both a high level of protection and an increase in productivity.
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