BioLife Solutions Expands Scientific Advisory Board
Adds Cell Therapy Regulatory Consultant and Cryopreservation Expert
PRNewswire-FirstCall
BOTHELL, Wash.

BioLife Solutions, Inc. (BULLETIN BOARD: BLFS) , a leading developer and marketer of proprietary hypothermic storage and cryopreservation media products for cells, tissues, and organs, today announced the expansion of its Scientific Advisory Board (SAB) with the addition of two leading experts in cell therapy quality and regulatory assurance and in cryopreservation of stem cells derived from cord blood, dental pulp, and other sources.

  The new members are:

  -- Scott R. Burger, MD - Principal of Advanced Cell and Gene Therapy, a
     consulting firm specializing in cell, gene, and tissue-based therapies.
     Dr. Burger works with clients in industry and academic centers
     worldwide, providing assistance in process development and validation,
     GMP/GTP manufacturing, GMP facility design and operation, regulatory
     affairs, technology evaluation, and strategic analysis. He received his
     M.D. from the University of Pennsylvania School of Medicine and
     completed postgraduate training in Laboratory Medicine and a clinical
     fellowship in Transfusion Medicine and a postdoctoral research
     fellowship at Washington University in St. Louis. He serves on the USP
     Cell, Gene and Tissue Therapies Expert Committee, the advisory boards
     of several cell therapy biotechnology companies, and has served as
     editor of the International Society for Cellular Therapy Telegraft, and
     on the ISCT Executive Committee. A frequently invited speaker at
     industry and academic conferences, he is the author of more than 100
     scientific publications and presentations, and recipient of numerous
     honors and awards.

  -- Erik J. Woods, Ph.D. - Co-Founder, CEO and Laboratory Director of The
     Genesis Bank, a private cord blood bank, and also Director of Genome
     Resources, an anonymous donor and client depositor sperm bank. Both
     laboratories are FDA registered and CLIA compliant. Dr. Woods received
     his Bachelor of Arts degree in Biology from Indiana University in
     Bloomington. He then went on to study cryobiology and biomedical
     engineering at the Hillenbrand Biomedical Engineering Center at Purdue
     University in West Lafayette, Ind., where he earned a Doctor of
     Philosophy Degree. Dr. Woods then completed a Post Doctoral Fellowship
     at the Herman B Wells Center for Pediatric Research at the Indiana
     University School of Medicine in Indianapolis, where he developed
     enhanced methods for the cryopreservation and banking of umbilical cord
     blood derived stem cells. In 1997 Dr. Woods co-founded General
     BioTechnology LLC, the parent company of The Genesis Bank, to apply
     these techniques to practical applications.  He holds two patents, has
     published numerous scientific articles, reviews and book chapters, and
     is a member of many professional scientific societies, including the
     American Association of Blood Banks, the International Society for
     Cellular Therapy, and The Cell Transplant Society. Dr. Woods is also on
     the Board of Governors for the International Society for Cryobiology.
     In addition to his position with The Genesis Bank, Dr. Woods is an
     Adjunct Assistant Professor in the Department of Microbiology and
     Immunology at the Indiana University School of Medicine.

BioLife Chairman and CEO Mike Rice commented: "We're delighted that Scott and Erik have joined our board of scientific advisors. Their expertise and experience in the cell therapy and cord blood banking industries will greatly benefit our strategic planning process, research activities, and the creation of relevant product marketing messages to reinforce the benefits of our HypoThermosol® and CryoStor™ preservation media products in these key markets."

Drs Burger and Woods join current SAB members Shelly Heimfeld, Ph.D., Director of the Cellular Therapy Laboratory at the Fred Hutchinson Cancer Research Center; Dayong Gao, Ph.D., Professor of Mechanical and Biomedical Engineering at the University of Washington; Darin Weber, Ph.D., Senior Consultant, Cell and Gene Therapies at Biologics Consulting Group; Andrew Hinson, Vice President of Clinical and Regulatory Affairs at Symphony Medical; and Lizabeth Cardwell, Principal of Compliance Consulting.

About BioLife Solutions

BioLife Solutions develops, manufactures and markets patented hypothermic storage and cryopreservation solutions for cells, tissues, and organs. The Company's proprietary HypoThermosol® and CryoStor™ platform of solutions are marketed to academic and commercial organizations involved in cell therapy, tissue engineering, cord blood banking, drug discovery, and toxicology testing. BioLife's products are serum-free and protein-free, fully defined, and are formulated to reduce or prevent preservation-induced, delayed-onset cell damage and death. BioLife's enabling technology provides academic and clinical researchers significant improvements in post-thaw cell, tissue, and organ viability and function. For more information please visit http://www.biolifesolutions.com/.

This news release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. These forward-looking statements include any statements that relate to the intent, belief, plans or expectations of the Company or its management, or that are not a statement of historical fact. Any forward-looking statements in this news release are based on current expectations and beliefs and are subject to numerous risks and uncertainties that could cause actual results to differ materially. Some of the specific factors that could cause BioLife Solutions' actual results to differ materially are discussed in the Company's recent filings with the Securities and Exchange Commission. BioLife Solutions disclaims any obligation to update any forward-looking statements as a result of developments occurring after the date of this press release.

  Media Relations:                         Investor Relations:
  Len Hall                                 Matt Clawson
  Allen & Caron Inc.                       Allen & Caron Inc.
  (949) 474-4300                           (949) 474-4300
  len@allencaron.com                       matt@allencaron.com

First Call Analyst:
FCMN Contact: nathan@allencaron.com

SOURCE: BioLife Solutions, Inc.

CONTACT: Len Hall, len@allencaron.com, or Matt Clawson,
matt@allencaron.com, both of Allen & Caron Inc., +1-949-474-4300, for BioLife
Solutions, Inc.

We believe the promise of cell and gene therapies starts with the integrity of a single cell

Advancing the future of cell and gene therapy

The human body can heal itself. Cell and gene therapies are designed to augment the patient’s ability to fight disease but only if the living cells behind those therapies remain viable and functional throughout the production processes. At BioLife Solutions, our mission is to protect the integrity of cells and provide trusted tools, services, and expertise that can enable our customers to advance the development and delivery of cell and gene therapies. We believe the future of cell and gene therapies hinges on the integrity of every single cell and we are here to protect that promise.

We understand the technical demands of bioprocessing in this field, and our advanced biopreservation expertise, cell culture optimization products, innovative storage systems, and closed-system manufacturing solutions are designed to enhance process efficiency, maintain cellular viability, and ensure reproducibility at every stage. Whether scaling up from R&D, navigating clinical trials or optimizing cryopreservation protocols for commercial production, we provide the tools and experience to streamline your workflow and safeguard your therapies.

Work with experts who understand your biopreservation challenges

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Collaborative and comprehensive CDMO support

At BioLife Solutions, we partner with leading contract development and manufacturing organizations (CDMOs) to enhance their biopreservation and cell processing capabilities. By providing advanced tools, regulatory support, and process optimization strategies, we empower CDMOs to better serve therapy developers, ensuring quality, consistency, and scalability in cell therapy manufacturing.

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readiness

Navigating the complex regulatory landscape of cell and gene therapy requires a proactive approach. BioLife Solutions offers experienced regulatory support to help prepare your biopreservation and cell processing methods to meet global standards. From IND and BLA submissions to compliance with GMP, FDA, and EMA guidelines, our solutions help streamline approval pathways.

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Stay ahead with our comprehensive Evidence Library, a curated collection of scientific publications, white papers, and case studies demonstrating the efficacy of BioLife Solutions’ technologies. Access peer-reviewed research, real-world application data, and expert insights to support your bioprocessing and regulatory strategies.

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