Quality Manufacturing Leaders Shaping Regulatory & Compliance Landscapes
With less than three weeks to go, you’re running out of time to register for the ISPE/FDA/PQRI Quality Manufacturing Conference, the most significant regulatory event of the year. This year’s conference, co-sponsored by FDA and PQRI, will again deliver the opportunity to interact directly with regulators and learn about current and future regulations.
“This year’s quality manufacturing conference includes topics that are on everyone’s agenda for 2016. Current supply chain challenges, cultivating a continuous improvement culture, innovation, measuring quality, operational excellence, and data integrity.” ~ Richard Friedman, Deputy Director, Science and Regulatory Policy FDA/CDER/OC/OMQ
Interactive sessions, developed in conjunction with co-sponsors, the FDA and PQRI, include a breakfast with the Investigators and the Industry and Regulatory Forum, allowing you to engage in direct dialogue with the regulators. These sessions offer the unique opportunity to have your questions answered by Quality Manufacturing leaders —and to be able to take that critical information back to your company.
“The FDA’s progress in GMP, program alignment & pharmaceutical operation excellence” will be discussed at the 2016 ISPE/FDA/PQRI Quality Manufacturing Conference.
~ Lawrence Yu, PhD, Deputy Director, FDA/CDER/OPQ
“As the world’s largest healthcare manufacturer, Johnson & Johnson has a long-standing legacy of commitment and partnership with industry associations and Health Authorities to enhance worldwide public health. Quality is built into our culture and opportunities for collective engagement, such as found at the ISPE/FDA/PQRI Quality Manufacturing Conference, help advance our holistic approach and harness the collective expertise, passion, and compassion from industry, academia, and the government. It is a tremendous honor for J&J to be invited to contribute to the meeting and by working together we can garner many more comprehensive insights on areas of importance to the health and wellbeing of patients and consumers around the world.”
~ François Sallans, Vice President and Chief Quality Officer of Johnson & Johnson
“Once again ISPE has assembled an extraordinary group of technical and regulatory experts engaged in deliberation of contemporary issues associated with pharmaceutical quality. The technical content in this conference reflects the breadth of complexity and variety of solutions that make this industry so dynamic.”
~ Roger Nosal, PhD, Vice President, Global Chemistry, Manufacturing & Controls (GCMC), Pfizer Inc.
Who should attend? Anyone working in Regulatory Affairs, Quality, Manufacturing, Research & Development, and Assurance/Control should not miss this conference.
Register for the 2016 ISPE/FDA/PQRI Quality Manufacturing Conference today and take advantage of the opportunity to interact with quality manufacturing leaders!