Our experts can perform GMP batch release testing to ensure your products are the highest quality of pharmaceuticals/biopharmaceuticals before sale, supply or export and to help make sure they are regulatory compliant. Our state-of-the-art analytical facilities support testing to ensure products meet specifications within the marketing authorization (MA) or Clinical Trial Dossier (CTD). Our dedicated service is extended beyond our labs with our method transfer and analyst exchange services to make sure QC procedures are smoothly integrated into your production environment.

At Lucideon our experts can identify, assay and determine the quality, purity and stability of your raw materials to be used in manufacture. Analysis can be carried out in accordance with pharmacopoeial monographs (Ph. Eur., BP, USP and JP) and/or to your specifications.

Whatever your needs please get in touch and our team will be able to help.