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Testing

In the complex drug development pipeline, there are several key areas where a need for product or materials testing becomes necessary. BioConvergence has a unique niche for delivering these testing capabilities to those in need, with a specialty in parenteral product testing. Additionally, we offer many tests suitable for a variety of dosage forms. Our testing services include:

  • Raw materials, in-process, and finished product release and stability testing
  • Product specific and compendial methods
  • Method transfer, trouble-shooting, optimization, qualification, and validation
  • Primary and secondary packaging components inspection (physical and dimensional)
  • Thermal cycling/excursion storage and analysis

Our experienced team can work with you to optimize your pharmaceutical product evolution testing capabilities. BioConvergence delivers solutions and results that can be securely and transparently viewed by our clients using our Electronic Laboratory Notebook System (ELN).


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Real solutions that our team has delivered through our testing services include:

  • Reliable on-time release and ICH stability studies supporting clinical trials
  • Efficient sourcing, storage, sampling, and testing of raw materials consolidated at a single location
  • Support of transportation temperature variations through thermal cycling/excursion studies


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ICH Chambers

  • -20 ± 5°C / Ambient
  • 5 ± 3°C / Ambient
  • 25 ± 2°C / 60 ± 5% RH
  • 40 ± 2°C / 75 ± 5% RH
  • 60 ± 2°C / 75 ±5% RH

A Few of Our Common Analytical Methods

  • Moisture Content (Karl Fischer)
  • Appearance
  • pH
  • Osmolality
  • Density
  • UV-Vis Spectroscopy
  • FTIR Spectroscopy
  • Bacterial Endotoxin
  • SDS – PAGE
  • HPLC
  • CE
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