Access quality and regulatory affairs knowledge and support. Get in the know.
Strong quality controls start with a system. Does your business need support to establish these processes? Who on your team is supporting your documentation controls initiatives? QUARA can serve as an extension of your business by managing quality systems and regulatory affairs. We can provide the education and training curriculum for business teams to form a foundation for strong quality and regulatory affairs practices.
Educate your team.
Get the training support your business needs as a player in the medical device, life sciences or biomedical industry. QUARA develops custom curriculum and serves as a partner you can depend on for ongoing updates about the topics mattering most to your business.
- Inspection and Audit Readiness
- FDA’s QSIT (Quality System Inspection Technique) Readiness
- Process Best Practices
- Design and Documentation Controls
- U.S. and International Quality System/Regulatory Compliance
- Tailored Training Programs
- Quality Refresher Courses