Quality

The framework we work to

Production is placed only with partners operating to recognised food or pharmaceutical manufacturing standards. Incoming materials are released against specification with a certificate of analysis, and material that does not meet specification is not taken into production.

Each batch is identified and retained, so a finished capsule can be traced back to the shell lot, the blend and the filling run that produced it. Stability is established on the finished capsule in its final packaging rather than on the blend alone, using accelerated and real-time studies, and shelf life is set on that basis. Disintegration is checked as a batch release test alongside fill weight and seal integrity.