Matrix Medical Devices Announces Team Additions
Mentor, Ohio April 21, 2015 – In response to increasing demand and planned business growth, Matrix Medical Devices (www.matrixmedicaldevices.com) announces new additions to its Team of regulatory and quality professionals. In order to provide a greater breadth and depth of expertise to our Clients, and our dedication to quality service, we are happy to introduce Meera Juneja and Kristi Musgrave.
Meera Juneja joins the Team as Principal Consultant, Regulatory Affairs and Quality Assurance. Meera brings with her over 15 years of medical device industry experience. She has led software validation compliance efforts, served as Management Representative for medical device product development cross-functional programs, maintained international and FDA regulatory requirements, and streamlined Document Control and Management Review process.
Kristi Musgrave joins the Team with over 17 years of experience in FDA regulated industries. As a Matrix Principal Consultant, Kristi’s proficiencies in developing quality management systems; training programs; and remediation efforts, will ensure Matrix’s ongoing efficiency and effectiveness for its Clients. Her technical knowledge, coupled with FDA experience, spans the medical industry to include biologics, drugs, medical devices and dietary supplements. Her demonstrated strength in quality system document preparation, learning management systems, purchasing controls, regulatory responses and validation protocols are significant achievements.
“We are delighted to welcome Meera and Kristi to the Team,” said Stephanie Harrington, CEO. “We are seeing an increasing need from our Clients to not just provide Solutions, but also to ‘parachute in’ Matrix Team members to help execute the Implementation, to meet Product Development or Corporate objectives. Both Meera and Kristi will help Matrix fulfill its Clients’ requests, while maintaining our expected Quality of Services.”
About Matrix Medical Devices.
Matrix Medical Devices was founded in July 2013 by Stephanie Harrington, to help provide Medical Device Product Development expertise to accelerate its Client’s product development cycle while streamlining post-market surveillance activities. Matrix Medical Devices offers both strategic and tactical support and currently serves as the in-house regulatory staff for numerous medical products companies. Since its formation in July 2013, Matrix Medical has grown steadily to support both start-ups and large institutions, from across the globe, including such places as Ohio, California, Florida, Canada, and Israel. In August 2014 Matrix Medical Devices entered into a Business Transfer Agreement with REU Associates Inc., to offer Clients a greater range of expertise, from an integrated Consultancy staff of Matrix Medical and REU Associates, including Ray Ursick, Founder of REU Associates, as well as a network of support contractors and partners. REU Associates Inc. was founded in September 2001 and established an industry reputation in providing responsive FDA and regulatory guidance on submissions and compliance requirements for the medical industry.
For more information, contact:
Ms. Josephine Matic, Director of Client Services and Operations