ISO 13485 is the international quality management standard and 21 CFR Part 820 is the U.S. legal requirement for organizations involved in the design, production, installation, and servicing of medical devices. This training usually costs between $1050 – $3150 and is only offered in larger cluster cities, forcing companies not located in the area to incur travel expenses for multiple days in order to complete this training.
It is due to these challenges that BioMedSA and PSC Biotech are proud to announce this month’s featured cost savings opportunity providing medical device companies the ability to participate in an ISO 13485/21 CFR 820 training on May 19 – 20 in San Antonio, Texas.
We have subsidized this training keeping the price well under the industry average, to benefit all area companies wanting to participate without costly travel expenses. The training will be offered with 1-day and 2-day options. Day 1 provides an overview of the regulatory requirements, with the optional Day 2 covering practical small company implementation strategies. Jorge Sugranes, a certified lead auditor with over 36 years of experience in quality training, will be instructing this course.
We are unfortunately having to limit the number of participants attending the course, so make sure you don’t wait to reserve your seat to this FDA/EU training.
For more information and to sign up for the 1 day course visit: https://biomedsa.org/events/medtech-quality-requirements-iso-13485-overview-course-1-day/
For more information and to sign up for both days, visit: https://biomedsa.org/events/medtech-quality-requirements-iso-13485-overview-course-1-day-308/