CfPIE Discusses Life Sciences Training Advancements at Regulatory Conferences

October 22, 2015
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Technical training advisors will offer insights and guidance at the annual conference for RAPS and BioOhio


Malvern, PA - October 22, 2015 - The Center for Professional Innovation and Education (CfPIE), the global leader of technical training across the life sciences industry, will participate at the upcoming 2015 regulatory conferences:

  • Mark Mazzie, CEO at CfPIE, will join a panel at the BioOhio Annual Conference in Cleveland, OH to discuss Talent, Training and Millennials. The number one issue affecting growth of any company is finding the right talent, and then these employees need ongoing skills and often leadership training. Mark and the panel will address finding and training talent, and how best to integrate millennials in the workplace.
  • At the Regulatory Affairs Professionals Society (RAPS) annual conference in Baltimore, MD training advisors from CfPIE will showcase and discuss their latest technical training courses and certifications for professionals across four segments— pharmaceuticals, biotechnology, medical devices, and skin/cosmetics. CfPIE courses are RAPS-approved. Attendees earn Regulatory Affairs Certification (RAC) credits through RAPS. Learn more at Booth 224.


"Our training advisors and industry-active course directors address specific situations and help individuals and groups make the right choices for technical training in their organizations," explains Mark Mazzie at CfPIE. "Annual events like RAPS and BioOhio allow us to spend quality time one-on-one to listen to their needs and shape our curriculum."


"We are very excited about our new medical device course and how it responds to FDA findings with CAPA systems," says Mark Mazzie, CEO at CfPIE. "Our industry-active instruction and dynamic learning format will prepare participants to be informed and effective for their organizations."


A sample of popular CfPIE course topics include: Adverse drug events; Best practices (GCP, GLP, GMP); Clinical trials; Design control principles; FDA regulatory compliance; Process validation; and Quality assurance and quality control.


Learn more about CfPIE's training courses and certifications.

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