Pharmaceutical Quality Control Testing

Lucideon’s pharmaceutical quality control testing and validation laboratories are fitted with state-of-the-art analytical equipment and testing facilities.  Our team of highly qualified and experienced technical staff will work with you to develop and deliver testing and analytical solutions to add value to your product or project.  We specialise in a range of chemical and microbiological testing capabilities as shown below.

We are fully GMP certified for quality control testing of human and veterinary medicinal products (full documentation is available to download on the right of this page). All Lucideon’s services are undertaken in compliance with EU guidance on GMP as it applies to contract QC testing laboratories.

We are MHRA-inspected (successfully re-accredited in September 2016), and a UKAS accredited testing house (No. 0013), so you can trust that the test data that we provide to you is accurate and reliable.  Our highly qualified and experienced technical staff use transparent, traceable, calibrated techniques and state-of-the-art equipment.

We have registered (self-identified) with the FDA (U.S. Food and Drugs Administration).  Please see our certificate here

Pharmaceutical Chemistry

Pharmaceutical Microbiology

Product Validation

Our complete product validation service is supported by a wide range of analytical capabilities, including advanced surface analysis, and expert knowledge, offering you:

  • patent infringement support - providing independent analysis
  • cleaning validation – ensure your product meets the strict cleanliness requirements using our cleaning validation service, VALIDATA
  • counterfeit drug detection – quick and effective detection using surface analysis techniques

Lucideon develop materials, methods and innovative in-house technologies for the pharmaceutical industry, including our novel drug delivery technologies.


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Resources

  • White paper

    Additive Manufacturing - A Metallurgical Perspective

    pdf 4 MB

  • White paper

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

    pdf 249 KB

  • White paper

    Quality by Design for the Pharmaceutical Industry

    pdf 835 KB

  • White paper

    Abuse Deterrence for the Pharmaceutical Market

    pdf 2 MB

  • White paper

    Surface Analysis Exposes Counterfeit Medicines

    pdf 479 KB

  • Newsletter

    Pharmaceutical Newsletter

    pdf 418 KB

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