Develop • Deliver • Innovate
Call Us: 1.812.961.1700

Develop. Deliver. Innovate.

BioConvergence is a trusted and transparent contract service provider for the pharmaceutical and biotechnology industries. Our vision is to accelerate the drug development process to provide life-saving solutions for patients in need. Every day, we work toward realizing this vision as our clients count on us to:

Develop. Each of our clients has unique projects and challenges. Our response is to develop customized solutions that add savings to the timeline and bottom-line.

Find out how this solution conserved scarce drug substance, while reducing the development timeline:

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Deliver. Whether we deliver data from the lab or clinical trial products to patients, we do so with accuracy and agility.

Find out how BioConvergence yielded a 99.7% excursion-free rate through implementing 5 innovative steps, and how your organization can too:

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Innovate. We continually seek opportunities to innovate systems and processes to better serve our clients. This mindset led to the creation of E-Transparency®.

Learn how E-Transparency® provides clients with 24/7 access to their products:
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How Can BioConvergence Help You?

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Supply Chain

Pre-Clinical Development Services:
  • Pre-formulation, Excipient, and Formulation Studies
  • Solubility, pH, Degradation, Potency, Thermal Analysis, etc.
  • Vehicle Delivery Studies (e.g.: Emulsion vs. Suspension vs. Solution)
  • Process Development
  • Lyophilization
  • Particle Size Reduction
  • Tech Transfer
Analytical Method Development Services:
  • Method Transfer
  • Optimization
  • Qualification
  • Validation
    • Examples: HPLC, UV-Vis, CE
Testing Services:
  • ICH Thermal Stability Test Programs
  • Compendial Testing
  • Trials for Solubility, pH, Degradation, Potency, Purity, Reconstitution, etc.
  • Raw Material Testing for Manufacturing Use
  • Thermal Cycling and Excursion Testing
  • Materials Compatibility Testing
  • Packaging and Container Component Physical Inspection
Production Services:
  • Labeling and Re-labeling
  • Kitting and Re-kitting
  • Secondary Packaging
  • Customized Secondary Packaging Design
  • Time Out of Refrigeration Tracking
  • cGMP Compliant
  • Pre-Clinical Studies
  • Clinical Trials
  • Blinded Studies
  • Commercial Products
  • Mergers & Acquisition Re-packaging Requirements
Supply Chain Services:
  • Management of Material Flow from Source to Final Destination Point
  • Distribution of Clinical Trial Materials
  • GMP Compliant, Controlled Environment Warehousing and Storage Facility
    • Multiple storage conditions: CRT (15-25°C), 2-8°C, -20°C, -80°C
    • Hazardous, Flammable, and Toxic Material Handling Capability
    • Controlled Substance Storage
  • Sampling and Dispensing/Aliquot of Bulk Materials
  • Cold Chain Mapping and Design
  • Shipper Qualification
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