Qualio Focuses on Building a New, Collaborative Life Sciences Ecosystem
(Qualio: San Francisco) -- Qualio
Exemplar Global and QLBS Partner to Launch Audit Simulator
(Exemplar Global: Milwaukee) -- Just like aviation flight simulators, the Audit Simulator provides opportunities to audit without risk.
Greenlight Guru Launches Greenlight Guru Academy
(Greenlight Guru: Indianapolis) -- Greenlight Guru, the leading medical device quality management software (MDQMS) platform, announces the launch of
Study Finds Quality Shifting From Operational Compliance to Strategic Business Driver
(ETQ: Boston) -- ETQ, a leading provider of quality management solutions, released findings from a first-of-its-kind research study–“The State of Quality Management: 2020.” According to the survey, companies are investing more in quality as a strategic business growth initiative that brings a sig
Greenlight Guru Updates Risk Management to Align With ISO 14971:2019
(Greenlight Guru: Indianapolis) -- Greenlight Guru, creator of the only quality management software designed specifically for the medical device industry, announces new software platform updates to align with the recently updated ISO 14971
Greenlight Guru Announces New Integration With Jira Software
(Greenlight Guru: Indianapolis) -- Greenlight Guru, the only quality management software platform designed specifically for medical device companies, announces a new integration with
FDA Opens Voluntary Qualified Importer Program (VQIP) Application Portal
(ANSI: Washington, D.C.) -- The American National Standards Institute (ANSI), a recognized accreditation body under the U.S.
IVT’s Validation Week 2018
(CBI UBM: Burlington, MA) -- IVT Network, the trusted source for life sciences validation and compliance knowledge, is featuring its flagship event, the 24th Annual Validation Week Oct. 22–24, 2018, in San Diego.
FDA Plans to Use ISO 13485 for Medical Devices Regulation
(ISO: Geneva) -- The Food and Drug Administration (FDA), an agency within the U.S.
