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  The Laboratory for Personalized Molecular Medicine^® (LabPMM^®) at Invivoscribe offer internationally standardized testing of novel and proprietary biomarkers that are critically important for patient care.
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  Accredited & Proven, Registered Medical Device Establishment, Multiple CDx Approvals, CE-marked IVDs, and Marketing Authorization Holder (MAH)
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  We take pride in expanding the science that bridges personalized medicine with quality healthcare.
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  Personalized Molecular Medicine^® is use of genomics and patient specific information to identify optimal treatment for each patient.
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PUBLICATIONS
- Featured Publication
  November 17th, 2020
  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
  VIEW PUBLICATION ⟶
- Latest Publications
  April 20th, 2021
  Validation of a Next-Generation Sequencing-based T-Cell Receptor Gamma Gene Rearrangement Diagnostic Assay: Transitioning from Capillary Electrophoresis to Next-Generation Sequencing
  VIEW PUBLICATION ⟶
  November 17th, 2020
  Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing
  VIEW PUBLICATION ⟶
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  San Diego, CA, US
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  Shanghai, China
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  San Diego, CA, US
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  Munich, Germany
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  Kawasaki, Japan
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  Shanghai, China
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  Invivoscribe Diagnostic Technologies,(Shanghai) Co.,Ltd.
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Next Generation Dx Summit

admin2021-09-07T18:48:08+00:00September 2nd, 2021|Conferences|

SOHO 2021

admin2021-09-07T18:47:31+00:00September 2nd, 2021|Conferences|

AGBT 2021

admin2021-09-07T18:47:37+00:00September 2nd, 2021|Conferences|

JSLH 2021

admin2021-09-07T18:45:23+00:00September 2nd, 2021|Conferences|

GFHC Congress

admin2021-09-07T18:48:46+00:00September 2nd, 2021|Conferences|

JSH 2021

admin2021-09-07T18:48:51+00:00September 2nd, 2021|Conferences|

JCA 2021

admin2021-09-07T18:46:02+00:00September 2nd, 2021|Conferences|

AMP 2021

admin2021-09-07T18:49:47+00:00February 26th, 2021|Conferences|

ASH 2021

admin2021-09-07T18:49:41+00:00February 26th, 2021|Conferences|

AMP EUROPE 2021

admin2021-03-01T20:21:22+00:00February 26th, 2021|Conferences|

Invivoscribe provides a full range of standardized CE-marked in vitro diagnostic cGMP products for hematology-oncology, as well as RUO assays, analyte specific reagents (ASRs), and DNA & RNA controls.

The Laboratory for Personalized Molecular Medicine® (LabPMM®) at Invivoscribe offer internationally standardized testing of novel and proprietary biomarkers that are critically important for patient care.

Browse our comprehensive menu of product & testing services.

A proven strategy to acceleratedrug approvals

Design Controls, Bioinformatics Software, Identify & Track, Custom Development, and Complementary MRD Assays

cGMP Compliant, CE-marked IVDs & CDx Manufacturing, Assay Development, and Controls & Reagents

Clinical Lab Experience, Internationally Standardized, Comprehensive Panels, Complementary MRD Assays, and Worldwide Enrollment

Accredited & Proven, Registered Medical Device Establishment, Multiple CDx Approvals, CE-marked IVDs, and Marketing Authorization Holder (MAH)

We take pride in expanding the science that bridges personalized medicine with quality healthcare.

Personalized Molecular Medicine® is use of genomics and patient specific information to identify optimal treatment for each patient.

November 17th, 2020 Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing

April 20th, 2021 Validation of a Next-Generation Sequencing-based T-Cell Receptor Gamma Gene Rearrangement Diagnostic Assay: Transitioning from Capillary Electrophoresis to Next-Generation Sequencing

November 17th, 2020 Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing

The Laboratory for Personalized Molecular Medicine^® (LabPMM^®) at Invivoscribe offer internationally standardized testing of novel and proprietary biomarkers that are critically important for patient care.

A proven strategy to accelerate
drug approvals

Personalized Molecular Medicine^® is use of genomics and patient specific information to identify optimal treatment for each patient.

November 17th, 2020
Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing

April 20th, 2021
Validation of a Next-Generation Sequencing-based T-Cell Receptor Gamma Gene Rearrangement Diagnostic Assay: Transitioning from Capillary Electrophoresis to Next-Generation Sequencing

November 17th, 2020
Routine Evaluation of Minimal Residual Disease in Myeloma Using Next-Generation Sequencing Clonality Testing