The GMP board game that tests and improves your GMP compliance, knowledge, attitude and awareness!
The GMP Handbook for pharmaceuticals
Quality Systems Handbook for MedDev
E-books: US and EU regulations
GMP translations (FR, SE, DK)
Search tool and document library. Find your way in regulations, guides and other reference documents.
Tammy Pelnik is a quality systems consultant and President of The St. Vrain Group, Inc., a management and technology consulting firm. She works with client firms to establish cost-effective quality systems and innovative process improvement plans. She provides staff assessment/enhancement planning and “crisis” project management services for product development efforts. Ms. Pelnik has significant experience in developing integrated Quality Systems and development processes for combination products. Prior to joining The St. Vrain Group, Inc., Ms. Pelnik was a Senior QA Manager with an international Class III device firm.
Ms. Pelnik is an ASQ Certified Quality Manager and Certified Quality Engineer, IRCA QMS Principal Auditor and holds a MS degree in computer science. Ms. Pelnik sits on AAMI’s Board of Directors. She has served on the Biomedical Instrumentation and Technology Editorial Board, the Regulatory Affairs Professionals’ Rocky Mountain Chapter steering committee and the ASQ Boulder Section’s leadership team. She has published articles in Regulatory Affairs Focus, Medical Device and Diagnostic Industry, Software Quality Journal, Biomedical Instrumentation & Technology and numerous conference proceedings.
![]()
For more information about AAMI, click the logo below:
» Corrective and Preventive Action (CAPA) Requirements and Industry Practice #5308
