The innovation-driven CDMO for Investigational Medicinal Products

At Custom, we are dedicated to attending the most influential events that cater to industry professionals and clients alike. Through these events, we aim to further our knowledge, information sharing, networking opportunities, and showcase the advancements and innovations within our company. Events are a key part of the Custom calendar in order to support our vision of discovery, collaboration, and growth in the world of pharmaceutical manufacturing.

Our formulation development starts with the end in mind: we work with you to define your drug product Quality Target Product Profile

We specialise in method development and validation, finished product quality control, raw materials testing, and stability evaluation. We follow a scientific and risk-based approach to develop and maintain analytical procedures used to test and characterize pharmaceutical products.

We conduct comprehensive stability studies following international guidelines, including ICH and regional regulatory requirements. We design these studies to assess the effects of various environmental conditions on products, such as temperature, humidity, and light.

We can manufacture important batches of drug product and placebo-to-match for Phase I, Phase II and Phase III clinical trials, supporting this crucial stage of new medicine development and patient therapy.

We can offer a Commercial Manufacturing and Packaging solution that will fit the needs of your product in our MHRA approved facility. With various options on solid dose form and both blister and bottle packs we know we know we can meet you manufacturing and packaging needs.