CANTON, Mich.– MMS Holdings (MMS) – an award-winning, data-focused CRO – announced that its learning arm, MMS Academy, has expanded its global training portfolio with the launch of new courses in inspection readiness and clinical programming. These new courses – created by industry-trained subject matter experts – will give students and working professionals the opportunity to gain the critical knowledge that the pharmaceutical, biotechnology, and medical device industries require.
In the 14-week inspection readiness course, students will gain an understanding of global health authority (i.e. FDA, EMA, etc.) inspection processes, targeted industry-specific guidance, and important regulations and guidelines that allow teams to ensure successful regulatory authority inspections.
Mini courses are also available, each lasting three to four hours, and have been prepared with consideration for a variety of specific inspection needs, including: remote inspections, regulatory agency and ISO basics, post inspection management, GMP, Sponsor and CRO inspections, and more.
“Preparing for regulatory inspections is essential in our industry, creating a critical need to have actionable, tested training for life sciences professionals at all levels,” said Michelle Gayari, Executive Vice President, Global Operational Excellence and Innovation, MMS. “Being unprepared for one inspection is all it takes to greatly delay a new drug or therapy. The skills of those who take this course are set to gain will help prepare them for successful inspections and a more successful future.”
