GXPQS management has been providing GLP, GMP, and GCP on-site training programs for decades. Our trainers have practical Industry experience performing and/or overseeing the activities that are the basis for these training sessions and have presented to classes from less than 10 to more than 100 people. Training materials include a detailed agenda, a paper copy of the slides, detailed course notes and additional supporting reference material (i.e. copy of relevant regulations/guidance documents). Each training course participant receives a GXPQS training certificate signed by the instructor upon completion of the course.
Industry training courses are notoriously expensive. Our goal at GXPQS is to provide you with a combination of strategy development, execution methodologies, and practical, hands-on content and course materials that will enable you to get the most out of your training experience. We can provide training on-site or via webinar to anyone interested in learning at the most competitive price in the industry – making ongoing training accessible to consultants, students, and academicians and improving their knowledge of the complete requirements and process of how drugs are developed in our industry.
GXPQS training modules are based on relevant regulations, guidelines, and industry standards to assist drug development professionals, academicians, students, and people new to the industry. Attendees could include, Sponsor personnel including upper management, investigators, and site personnel; IRB or other oversight board members, CRO/CMP personnel; students from local universities, as well as CMC and Commercial operations staff.
Off the shelf training modules developed by GXPQS (webinars 1-3 hours)
Customized in depth training courses (2-3 day courses)
Clinical and Commercial Inspection Readiness Training