A specialised technology transfer team, combined with extensive expertise in scale-up and process validation means you can trust Pharmaserve NW to deliver the transition from small to large scale production. Our turn-key service includes every stage from material procurement through to on-site QP release, ensuring a reliable, consistent and cost effective solution, making Pharmaserve NW an ideal partner for the commercialisation of your product.
Our dedicated and experienced commercialisation experts ensure you can scale-up, validate and bring your product to market efficiently and cost effectively, thus achieving commercial success for your products. See below for details of our capabilities at each stage.
The process of transferring a technology (analytical methods, related specifications and experience) from Pharmaserve NW to an external company or vice versa.
The transition from small scale through to commercialisation, including the generation of documentation capable of supporting any product licence submission.
Analysis of the data generated from the design and manufacture of a product in order to confirm that a process is reliable, can conform to a determined standard and consistently generate high quality products.
Business management process that helps to optimise the supply chain to ensure the customer receives products on time and in full every time.
Strategically overseeing interactions with external goods/service suppliers to maximise the value of those interactions.
The manufacture of components or raw materials into finished goods.
The process intended to control a product and ensure that it is fit for purpose and conforms to defined quality specifications or the constraints of the client/customer.
Formal Qualified Person release of drug product either to clinic for investigations medicinal products or to market for authorised products.