home > news > detailed info

BioIVT Webinar Will Discuss How to Optimize Microbiome Research

Sample collection and processing techniques play a crucial role in ensuring that research results represent the complete microbiome

BioIVT, a leading provider of research models and services for drug development, today announced that it is hosting a webinar entitled “The Microbiome: Understanding Why Collection and Processing Matters” at 11 a.m. ET on July 25.

The human microbiome is comprised of all the microorganisms – whether beneficial, neutral or harmful – found in or on the human body.

“Since the Human Microbiome Project was launched in 2007, scientific knowledge and understanding of the human microbiome’s role in health and disease have grown dramatically. An individual’s microbiome is now known to impact their overall health, disease severity, and response to medications. In fact, a person’s microbiome is thought to be able to control their pathogens, immune system and mood!” said Mark Driscoll, PhD, Shoreline Biome co-founder.

“As we learn more about the potent impact that an individual’s microbiome can have on their overall health, the desire to harness it to improve health outcomes increases,” said Cathie G. Miller, PhD, BioIVT director of product marketing, personalized medicine. “To optimize microbiome research, scientists need access to high quality disease-state and control samples, which have been collected and processed using standardized, highly reproducible techniques. That is one of BioIVT’s areas of expertise.”

This webinar, which will be co-presented by Drs. Driscoll and Miller, will discuss best practices for securing representative samples of all microbes within a biospecimen.

Drs. Driscoll and Miller will outline optimal sample collection, processing and assay techniques. They will also discuss the importance of sample lysis and primer design and how to select the most appropriate sequencing platform and database mapping approach. In addition, they will review a case study with webinar attendees.

BioIVT has the largest network of IRB-approved sample collection sites in the industry, together with an extensive inventory of the highest quality disease-state and control biospecimens. Samples are available for a wide range of conditions, including Crohn’s disease, ulcerative colitis, irritable bowel disease, celiac disease, functional abdominal pain syndrome, and diarrhea. Furthermore, BioIVT works closely with its clients and has the ability to customize all aspects of its sample collection and storage processes.

Interested parties can register for this complimentary one-hour webinar at

About BioIVT

BioIVT, formerly BioreclamationIVT, is a leading global provider of research models and value-added research services for drug discovery and development. We specialize in control and disease-state biospecimens including human and animal tissues, cell products, blood and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research and the effort to improve patient outcomes by coupling comprehensive clinical data with donor samples. Our PHASEZERO® Research Services team works collaboratively with clients to provide target and biomarker validation, phenotypic assays to characterize novel therapeutics, clinical assay development and in vitro hepatic modeling solutions. And as the premier supplier of ADME-toxicology model systems, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly-discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service, and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in elevating science. For more information, please visit or follow the company on Twitter @BioIVT.
Print this page
Send to a friend
News and Press Releases

Realising the potential of single-use technology – As published in Manufacturing Chemist

In this article Zenith Technologies’ Global Director of Managed Services David Staunton and Scott Ripley, Global Marketing Director at GE Healthcare, discuss the benefits and patient impact of single-use technology with Manufacturing Chemist.
More info >>

White Papers

Key to Outsourcing Method Development and Validation A Pragmatic Approach


In an industry that is seeing an increasing level of work being outsourced, the Contract Research Organisation (CRO) of choice needs to have proven experience in both the pragmatism and flexibility of the method developer’s mind set and a regulatory background in validation.
More info >>

Industry Events

SMi Presents the 11th Adaptive Designs in Clinical Trials Conference 2019

1-2 April 2019, Holiday Inn Kensington Forum, London

SMi Group are proud to announce the 11th annual Adaptive Designs in Clinical Trials conference and exhibition will return to London from the 1st – 2nd April 2019. With the growing popularity in use and acceptance of adaptive designs in clinical trials - demonstrated most recently with the new FDA draft guidance on adaptive designs – there is a pressing need for a forum which explores this increasingly normalized medical methodology.
More info >>

©2000-2011 Samedan Ltd.
Add to favourites

Print this page

Send to a friend
Privacy statement