QC (batch release) and Raw Materials Testing

Using a wide range of chemical analysis techniques, we provide QC testing of raw materials, APIs, finished products, packaging materials and medical devices as outlined in marketing authorizations and pharmacopoeias.

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.

Applications of Field Enhanced Sintering

Got a question?

Contact us here

Resources

  • White paper

    Additive Manufacturing - A Metallurgical Perspective

    pdf 4 MB

  • White paper

    Are you Ready for USP <232>/<233>?

    pdf 249 KB

  • Newsletter

    Pharmaceutical Newsletter

    pdf 418 KB

Register or sign in below to access our resources.

Register

Forgot your password?