BioLife Solutions Expands Scientific Advisory Board with Cord Blood Specialist
Product Development Will Benefit From Input of Physician in Strategic Cell Therapy Market
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 addition of Colleen Delaney, MD, MSc to its Scientific Advisory Board (SAB).

Dr. Delaney is the Director of the Cord Blood Research and Transplant Program at Fred Hutchinson Cancer Research Center (FHCRC) and Seattle Cancer Care Alliance (SCCA). She is an attending physician at Seattle Children's Hospital, Assistant Member of the Clinical Research Division of FHCRC and Assistant Professor at the University of Washington School of Medicine. Dr. Delaney's research interests include hematopoietic stem cell regulation and the development of novel and clinically feasible ex vivo expansion systems for hematopoietic progenitor cells. Her goal is to improve the outcome of patients in need of a cord blood transplant. Dr. Delaney is principal investigator on five FHCRC clinical trials investigating the use of single or double unrelated donor umbilical cord blood grafts as an alternative source of stem cells for hematopoietic cell transplant, including a multi-center protocol investigating the use of single versus double unrelated donor umbilical cord blood grafts as source of stem cells for hematopoietic cells.

Dr. Delaney commented on her relationship with BioLife by stating, "I'm quite impressed with BioLife's technology. We're evaluating CryoStor™ for a potentially large scale cell bank application and so far, the increased quantity of functional cord blood derived stem cells that were frozen using CryoStor and the improvement in engraftment have been remarkable. I look forward to advising the company on a robust quality and regulatory strategy that could accelerate adoption of BioLife's products."

Chief Executive Mike Rice remarked on Dr. Delaney joining BioLife's SAB: "We're thrilled that Dr. Delaney has joined our Scientific Advisory Board. Her input on our product development and regulatory strategies will be extremely valuable as we continue to establish our biopreservation media products as new potential standards for clinical cell-based therapies sourced from cord and peripheral blood, where quality of production reagents, shelf life, process improvements, post-preservation function, and ultimately therapeutic efficacy are of great concern to manufacturers, hospitals, physicians, patients and payers."

About BioLife Solutions, Inc.:

BioLife Solutions develops and markets patented hypothermic storage/transport and cryopreservation media products for cells, tissues, and organs. The Company's proprietary HypoThermosol® and CryoStor™ platform of biopreservation media products are marketed to academic research institutions, hospitals, and commercial companies involved in cell therapy, tissue engineering, cord blood banking, drug discovery, and toxicology testing. BioLife's fully defined serum-free and protein-free products are manufactured under current Good Manufacturing Practices and are formulated using only USP or highest available grade components to reduce preservation-induced, delayed-onset cell damage and death. BioLife's enabling technology provides research and clinical organizations significant yield improvement in post-preservation cell and tissue and viability and function.

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 U.S. 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                        Dan Matsui
   Allen & Caron Inc               Allen & Caron Inc
   (949) 474-4300                  (949) 474-4300
   len@allencaron.com              d.matsui@allencaron.com

First Call Analyst:
FCMN Contact:

SOURCE: BioLife Solutions, Inc.

CONTACT: Media Relations, Len Hall, len@allencaron.com, or Investor
Relations, Dan Matsui, d.matsui@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.

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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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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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