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Raymond M. Pizinger

Dir , Regulatory Affairs and Quality Assurance at Aspyra, LLC

Raymond M. Pizinger has over 30 years of hands-on professional experience in the fields of Best Business Practices, Quality Systems, Worldwide Regulatory Compliance and Submission, Quality Assurance, Engineering, Operation. Directed quality organizations through start-up, mergers, acquisitions, divestitures, IPO’s and OEM alliances. He has an extensive experience in the Medical Device Industry as an executive, consultant and international trainer.

Provides leadership, guidance and oversight to all plants within the worldwide business to ensure consistency of Quality programs, policies, funding and procedures and to ensure maintenance of an outstanding level of global Regulatory compliance.

Has helped many companies prepare for FDA inspections as well as helped companies that didn't prepare and had to respond to FDA with corrective action plans that would resolve the FDA observations raised during the inspection. The later is much more difficult than good preparation.



  •  Tuesday, September 29, 2020
  • 10:00 AM PDT | 01:00 PM EDT,
  • 60 Minutes
  • $110.00
Establishing a Product Software Validation Process

The training provides insight into what is required to implement an effective software validation process for product software. Then explore what is required for software validation that is integral to automated business processes.

  •  Thursday, October 8, 2020
  • 10:00 AM PDT | 01:00 PM EDT,
  • 60 Minutes
  • $110.00
Establishing a Workable Complaint System and Medical Device Reporting Process

The training provides insight into FDA requirements for an effective complaint system





  • Recorded
  • View Anytime
  • 60 Minutes
  • $150.00
Establishing a Product Software Validation Process

The training provides insight into what is required to implement an effective software validation process for product software. Then explore what is required for software validation that is integral to automated business processes.

  • Recorded
  • View Anytime
  • 60 Minutes
  • $150.00
Establishing a Workable Complaint System and Medical Device Reporting Process

The training provides insight into FDA requirements for an effective complaint system