Pharmaceutical >> Quality Control >> Pharmaceutical Release Testing

Pharmaceutical Release Testing

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To support your commercial product and clinical trial material release testing needs, Eurofins BioPharma Product Testing offers the capacity and breadth of capabilities to test your drug substance, drug product or in-process materials in a timely manner.

We test materials against specification for identity, potency, impurities, physical properties and safety under strict cGMP compliance, and we customize individual programs to streamline lab documentation and reporting for the most efficient and quality-focused data deliverable possible.

Our multi-shift laboratory operations are designed to provide extensive capacity for larger volume release programs, as well as flexibility for smaller programs in a manner that allows for aggressive cycle times.

Why Choose Eurofins BioPharma Product Testing?

  • We have in-depth experience working with every type of modality and have the flexibility and extensive  instrument capacity within our team to meet  the ever-changing demands of production schedules and timelines.
  • Our breadth of capabilities allows us to perform all  testing of even the most complex molecules at one  laboratory location, helping to minimize the time  between production and release. This includes chemical and microbiological testing, as well as  more specialized testing such as pyrogen, antibiotic potency, bioassay and toxicity testing.
  • Our network of global facilities allows us to support your EU batch release requirements.

Instrumentation

  • LC/MS/MS
  • HPLC/UPLC
  • GC
  • IC
  • GPC
  • GC/MS
  • KF
  • SEC
  • TOC
  • Dissolution Baths: Apparatus 1,2,5 & 7-Distek/Agilent-(formerly Varian)

Our Experience Includes

  • Capsules (IR/SR)
  • Contact Lenses
  • Implantables (including stents, coronary sleeve and pacemakers)
  • Injectables
  • Inhalers
  • Ocular Implants
  • Liquids
  • Patches
  • Suppositories
  • Suspensions
  • Synthetic Blood
  • Tablets (IR/SR)