Conventional bulk filling
Specify product condition, container presentation, fill quantity, closure and the next storage or processing step. The filler must suit the actual puree viscosity and package. Freezing or downstream preservation may sit outside the filling scope.
An aseptic assessment
Identify the formulation, process-authority requirements, thermal treatment and sterile product path. Confirm the proposed bag and fitment, sterile interface and controls as one connected system. Installing a filler alone does not establish commercial sterility.
Information that changes the proposal
Provide the package documentation, target fill mass, product temperature and intended storage route. Identify existing equipment and the supply handover. These determine which heating, transfer, controls and filling duties need assessment.
Compare commissioning responsibilities
Agree how the connected process, package handling and cleaning are verified. Separate mechanical commissioning from the validated product process. Exact time-temperature conditions and shelf-life claims require the relevant validated specification.
Prepare your project brief
What to share with your enquiry
- Formulation and preservation objective
- Package/fitment documentation and fill mass
- Existing thermal and sterile-transfer equipment
- Validation, commissioning and cleaning responsibilities