BIOVECTRA Inc. Invests $1.5M in Large-Scale Synthetic Reactor Replacements and Analytical Development Capabilities

BIOVECTRA Inc. Invests $1.5M in Large-Scale Synthetic Reactor Replacements and Analytical Development Capabilities

BIOVECTRA Inc., a global Contract Development and Manufacturing Organization (CDMO), today announced new investments in its large-scale synthetic chemistry and analytical development capabilities. To continue serving its client’s cGMP manufacturing needs, BIOVECTRA completed the replacement of two 4,000L vessels used for small molecule synthesis.

“These vessels have been very important for advancing our clients’ programs into later-stage clinical trials,” said Matt Frizzle, BIOVECTRA’s Director of Business Development, CMO Services. “They are highly critical when larger quantities of Active Pharmaceutical Ingredients (APIs) are needed and, in particular, through commercial supply.” For earlier stages of research, BIOVECTRA operates several cGMP kilo labs, with access to reactors in the range of 30-800L.

Additionally, BIOVECTRA announced an enhancement of its analytical capabilities through the purchase of new equipment. “These investments help ensure our process development team has adequate control and specifications to meet regulatory requirements,” said Dr. Marc Sauer, BIOVECTRA’s Vice President of Research and Development.  BIOVECTRA’s suite of analytical equipment will be bolstered with the addition of two UPLCs and five HPLCs, two Charged Aerosol Detectors (CAD), two single quad mass detectors, a XRPD unit, an ICP-MS, a particle surface area and a DSC/TGA instrument.

Combined these investments were in the order of $1.5M, and were made to enhance BIOVECTRA’s overall API service offering to our global biotechnology and pharmaceutical partners.

About BIOVECTRA

BIOVECTRA is a CDMO that serves global pharmaceutical and biotech companies with full-service cGMP outsourcing solutions for intermediates and active pharmaceutical ingredients. An innovative and reliable service partner with a strong regulatory history, BIOVECTRA has over 45 years of experience specializing in:

For more information about BIOVECTRA, please visit www.biovectra.com.

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  • 20+ years at GSK, leading R&D activities on multiple vaccine programs
  • Recently held positions in industry include: Senior Director (Function Head), Protein Biochemistry; Director, Antigen Design & Prototype Production; and, Associate Director, Antigen Design and Protein Characterization.
  • Key areas of expertise are:
    • Process development of protein Biologics/Recombinant Antigens
    • Recombinant protein expression (mammalian, insect, yeast, bacterial)
    • Production/design of Viral Vectors, mRNA vaccines, Bacterial outer membrane vesicles
    • Protein Engineering and Structural Biology
    • Defining quality attributes, biophysical characterization of proteins, and analytical strategy
  • Post graduate degrees in Functional Genomics (Université Laval) and Bioinformatics (MIT); M. Sc. Microbiology and Immunology (Laval).
  • 25+ Patent & 5 Scientific Publications