FDA News

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Honeywell Launches Product Quality Review Automation Application
Streamlines annual regulatory review for life sciences
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Cablevey Mobile ‘Smart Cart’ Automates Food Conveyor CIP
Facilitates quick sanitary compliance and production changeover
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ArisGlobal Signs Agreement to Acquire Amplexor Life Sciences
Creates one of the most comprehensive regulatory SaaS platforms for the industry
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MasterControl Raises $150M Series A Funding
Company’s first funding round will be used to accelerate product development for its QMS and MES SaaS offerings
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Husky Technologies Travels to Dubai
Showcasing tech, solutions, and services at Gulfood Manufacturing 2022
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Maintaining Quality Assurance in Pharmaceutical Packaging
Easy, reliable leak testing with methylene blue
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Supply Shortages Could Lead to Greater Food Fraud Risk
Now is not the time to skip critical factory audits and supply chain assessments
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ETQ Releases Reliance NXG QMS and New Quality Events Application
Google Docs collaboration, more efficient management of quality deviations
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Qualio Focuses on Building a New, Collaborative Life Sciences Ecosystem
Delivers time, cost, and efficiency savings while streamlining compliance activity
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Exemplar Global and QLBS Partner to Launch Audit Simulator
First trial module of learning tool focuses on ISO 9001 and is available now
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Greenlight Guru Launches Greenlight Guru Academy
Free education source for global medical device community
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Study Finds Quality Shifting From Operational Compliance to Strategic Business Driver
Good quality is adding an average of 11 percent to organizations’ revenue growth
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Greenlight Guru Updates Risk Management to Align With ISO 14971:2019
Further enhances change management capabilities
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Greenlight Guru Announces New Integration With Jira Software
Creates adaptive system for managing product development and post-market quality for devices with software elements
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FDA Opens Voluntary Qualified Importer Program (VQIP) Application Portal
VQIP allows for expedited review and importation for approved applicants that demonstrate safe supply chains
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IVT’s Validation Week 2018
An invite from Alcon Laboratories
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FDA Plans to Use ISO 13485 for Medical Devices Regulation
Intended to harmonize domestic and international requirements
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Pharma Companies Expect Role of Quality Management Teams to Evolve in 2018
Pharma quality teams will have performance-oriented objectives as well as regulatory compliance goals
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Hands-On Workshops at IVT’s Quality Risk Management and Change Control 2018
Feb. 27–March 1, 2018, in San Diego
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ETQ Announces Acquisition by TCV
Strategic investment positions EtQ to accelerate innovation efforts and growth strategy