Invivoscribe is a global, vertically-integrated biotechnology company dedicated to Improving Lives with Precision Diagnostics®. For nearly thirty years, they have been a leader in developing and commercializing a broad range of IVD products, clinical testing services (through their LabPMM laboratories), and bioinformatics software used in molecular diagnostics and personalized medicine. Their strong focus is on hematologic malignancies and MRD (Minimal Residual Disease) testing, offering solutions from Research Use Only (RUO) to In Vitro Diagnostic (IVD) products, supporting research, clinical trials, and routine clinical testing worldwide.
Serves as the global corporate headquarters, housing key operations including research and development, GMP manufacturing, CLIA/CAP accredited clinical laboratory services (LabPMM San Diego), and global administrative functions.
State-of-the-art laboratory facilities designed for advanced molecular diagnostics development, manufacturing, and high-complexity clinical testing. Includes capabilities for companion diagnostics development.
A science-driven, innovative, and collaborative environment focused on quality, precision, and making a tangible impact on patient care. Emphasizes meticulousness due to the nature of diagnostic testing and regulatory compliance.
The San Diego headquarters centralizes core strategic, operational, and R&D activities, benefiting from the rich biotech ecosystem, access to a skilled talent pool, and proximity to research institutions and partners.
Invivoscribe maintains a significant global presence, directly supporting clinical trials, research institutions, and diagnostic laboratories across North America, Europe, and Asia through its strategically located offices and laboratories (LabPMM). The company offers worldwide distribution of its Research Use Only (RUO) and In Vitro Diagnostic (IVD) products, engages in global companion diagnostics development partnerships, and provides internationally accessible clinical laboratory services. Its bioinformatics platforms are also utilized by laboratories globally, underscoring its commitment to improving patient care worldwide.
10222 Barnes Canyon Rd, Bldg 1
San Diego
CA
USA
Address: Lochhamer Str. 29A, 82152 Martinsried, Germany
Supports European customers, clinical trials, and commercial operations; ensures adherence to European regulatory standards (e.g., IVDR) and provides regional diagnostic services.
Address: Room 302, Building 1, No. 18, Ronghua Road East, Shanghai Pilot Free Trade Zone, Shanghai 200131, China
Facilitates market access and growth in China, supports local clinical research collaborations and addresses specific regional healthcare needs.
Address: Nihonbashi Life Science Building 2, Room 601, 2-3-11 Nihonbashi-honcho, Chuo-ku, Tokyo 103-0023, Japan
Addresses the specific requirements of the Japanese healthcare system and research community, managing local distribution channels and regulatory interactions.
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As of April 2025, Invivoscribe' leadership includes:
Invivoscribe has been backed by several prominent investors over the years, including:
Invivoscribe has strengthened its executive leadership over the past year, highlighted by the strategic appointment of a new Chief Medical Officer with extensive FDA experience. This move aligns with the company's growth trajectory and focus on clinical and regulatory excellence, particularly following its acquisition by Summa Equity in 2023. No major executive departures have been publicly announced during this period.
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Invivoscribe most likely utilizes a standard professional email format, commonly [first_initial][last_name]@invivoscribe.com. This format is prevalent in many companies, particularly in the biotechnology and healthcare sectors, for its simplicity and professionalism.
flast@invivoscribe.com
Format
jmiller@invivoscribe.com
Example
85%
Success rate
PR Newswire • January 9, 2024
Invivoscribe announced the strategic appointment of Tim Stenzel, M.D., Ph.D., as its new Chief Medical Officer. Dr. Stenzel, who previously served as the Director of the Office of In Vitro Diagnostics and Radiological Health (OIR) at the U.S. Food and Drug Administration (FDA), will guide Invivoscribe's clinical development and regulatory affairs....more
Business Wire • April 26, 2023
Summa Equity, a purpose-driven thematic investment firm, announced its acquisition of a majority stake in Invivoscribe. This partnership aims to accelerate Invivoscribe's mission to expand its global leadership in precision diagnostics for cancer and Minimal Residual Disease (MRD) testing, further enhancing its ability to improve patient outcomes....more
Invivoscribe News • December 7, 2023
At the 65th American Society of Hematology (ASH) Annual Meeting, Invivoscribe, in collaboration with The Leukemia & Lymphoma Society's Beat AML® Master Clinical Trial, presented significant data. The findings highlighted the clinical utility of Invivoscribe's LymphoTrack®, MyMoid® Track, and MyRaid® Myeloid Assays for comprehensive genomic profiling in acute myeloid leukemia (AML)....more
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