FARMINGDALE, NY (01-09-15): EtQ is pleased to announce that a pharmaceutical manufacturer has selected the EtQ Reliance GMP System. EtQ looks forward to demonstrating its value to this company by automating critical processes such as Corrective Action, Training and Production Part Approval Process (PPAP).
Life Science organizations that choose EtQ’s compliance management platform will benefit from capabilities such as electronic signature and electronic reporting. The flexibility of EtQ’s automated workflow platform makes common business processes easier while significantly reducing the time it takes to accomplish tasks.
For more information on EtQ’s products and services, contact us at firstname.lastname@example.org or 800.354.4476.
EtQ is the leading FDA Compliance, Quality, EHS and Operational Risk Management software provider for identifying, mitigating and preventing high-risk events through integration, automation and collaboration. Founded in 1992, EtQ has always had a unique knowledge of FDA Compliance, Quality, EHS and Operational Risk processes, and strives to make overall compliance operations and management systems better for businesses. EtQ is headquartered in Farmingdale, NY, with main offices located in the U.S. and Europe. EtQ has been providing software solutions to a variety of markets for more than 20 years. For more information, please visit https://www.etq.com or contact us at 800-354-4476.