Tampa, FL – February 28, 2013 -- Pilgrim Software, Inc., a world-leading provider of Enterprise Quality and Compliance software solutions, today announced it will be exhibiting at the 25th Annual Drug Information Association (DIA) EuroMeeting, “Advancing Therapeutic Innovation and Regulatory Science,” March 4-6, 2013, in Amsterdam.
DIA’s Annual EuroMeeting is global in scope and attracts well over 3,000 professionals from more than 50 countries. It brings together professionals from the biopharmaceutical industry, contract research and service organizations, academic research centers, regulatory agencies and health ministries, as well as delegates from patient organizations. This convergence affords participants the opportunity to network with professional colleagues from around the world.
With a focus on better public health protection, greater transparency of the processes and the rational use of medicinal products, the proposed areas for discussion for the EuroMeeting 2013 will include pharmacovigilance and regulatory affairs for medicinal products and medical devices, R&D and clinical trials. Speakers from the European Medicines Agency, the European Commission, the FDA, and other international regulatory agencies will provide updates on the current state of efforts impacting the development of global regulatory strategies.
“Pilgrim is looking forward to showcasing our enterprise quality and compliance management solutions at this year’s DIA EuroMeeting,” said Thierry Durand, Chief Executive Officer of Pilgrim Software. “Pilgrim provides a common framework and an integrated approach to meet pharmaceutical and biotech regulatory standards such as 21 CFR Part 210-211, GxP, ISO, ICH , as well as the industry-focused mandates and regulations from FDA, EMA, and global regulatory bodies, making it easier for companies to manage operational quality and compliance.”
Pilgrim’s SmartSolve® supports organizations’ quality and compliance processes with its fully integrated enterprise platform for managing corrective and preventive actions, nonconformances, customer complaints, SOPs and regulatory documents, training and certifications, and audits. This powerful and comprehensive closed-loop solution integrates and streamlines quality and compliance processes across your entire business - helping companies meet industry and regulatory requirements, increase efficiency and reduce costs.
For more information on Pilgrim Software’s solutions, visit Pilgrim at the DIA EuroMeeting in booth #728 or on the Web at http://www.pilgrimsoftware.com.
About DIA
Since its founding in 1964, the Drug Information Association (DIA) has evolved from a group of 30 professionals employed in academia and the pharmaceutical industry into a global, multidisciplinary association of nearly 18,000 members in more than 80 countries. Today, the DIA is the global forum for knowledge exchange that fosters innovation to raise the level of health and well-being worldwide. Website: http://www.diahome.org.
About Pilgrim Software, Inc.
Pilgrim Software, the world leader of cloud and on-premise enterprise solutions for quality and compliance management, delivers integrated applications for pre- through post-market operations of Life Sciences companies. For more than a decade, Pilgrim’s tightly integrated 21 CFR Part 11-compliant system has enabled its clients to proactively manage documents, audits, complaints, nonconformances, corrective/preventive actions, supplier quality, and training, helping ensure product safety and regulatory compliance, reduce manufacturing costs, and improve customer satisfaction. For more information, visit Pilgrim Software’s website at www.pilgrimsoftware.com.
