Global Operations

Founded in 2012 to help companies solve complex challenges ranging from ideation to high volume production. We operate in centers of excellence for manufacturing and health care delivery.

World Headquarters

World Headquarters

Cleveland, Ohio

Pre-Clinical Research

Pre-Clinical Research

Dublin, Ireland

Company Milestones

Viscus_Biologics_Company_History_Timeline

Our Core Values

The culture at Viscus Biologics emanates from core values shared by team members throughout the organization.

core values

 

Our Team

Peter Gingras

Peter Gingras

CEO

Peter Gingras

CEO

peter.gingras@viscusbiologics.com

+1 (216) 744-2741

Rebecca Clines

Rebecca Clines

VP Quality

Rebecca Clines

VP Quality

rebecca.clines@viscusbiologics.com

+1 (216) 744-2742

Robert Priest

Robert Priest

COO

Robert Priest

COO

robert.priest@viscusbiologics.com

+1 (216) 744-2743

Justin Baker, PhD

Justin Baker, PhD

VP R&D

Justin Baker, PhD

VP R&D

justin.baker@viscusbiologics.com

+1 (216) 744-2744

Nicole Fraifogl, PhD

Nicole Fraifogl, PhD

Senior Project Engineer

Nicole Fraifogl, PhD

Senior Project Engineer

nicole.fraifogl@viscusbiologics.com

+1 (216) 744-2740 ext. 707

Laura Schramm

Laura Schramm

Office Administrator

Laura Schramm

Office Administrator

laura.schramm@viscusbiologics.com

+1 (216) 744-2740 ext. 700

Quality Policy

Viscus Biologics, LLC designs, manufactures and delivers innovative medical devices with the objective of positively impacting the health and well-being of patients around the world. Given the nature of these products, Quality is of paramount importance in the culture and operation of the organization.

Accordingly, Viscus Biologics, LLC has established a Quality Management System in compliance with ISO 13485, FDA 21 CFR 820 and other appropriate national regulations to guide our actions and ensure safe and effective devices. Viscus Biologics, LLC, is committed to establishing a quality culture and providing quality products by:

  • Producing innovative and reliable medical devices and components that add value to the life science industry via a needs-based approach;
  • Providing unparalleled service to our customers;
  • Establishing and continually improving our Quality Management System that is in compliance with national and international regulations and standards, such as ISO 13485 and 21 CFR 820, and,
  • Establishing and regularly reviewing quality objectives.

Made in the USA, FDA compliant facility, GMP good manufacturing practicebsi ISO 13485 Medical Devices Quality Management