Precision Medical Products’ quality assurance philosophy focuses on defect prevention by utilizing statistical methods where appropriate to control processes. Product quality is the responsibility of the individuals performing the operations. Through training, education, and self improvement activities we are able to sustain a quality-minded work force aware of possible defects and empowered to resolve quality issues. PMP’s Customer Focused Approach is geared towards meeting both external and internal customer requirements.
All employees of PMP are committed to doing the right thing, the right way, all of the time, in order to meet or exceed our customer’s expectations.
This includes a commitment to comply with ISO 13485, FDA, OSHA, and other legal requirements as well as all ethical, quality, policy, procedure and company objective requirements, and to maintain the effectiveness of the quality management system.
PMP is a progressive FDA registered, medical device company with a quality system in compliance with Government Regulation 21 CFR Part 820, Quality System Regulation. We are also a certified ISO 13485:2003 company. The Total Quality Management (TQM) and Operational Excellence focus of the company provides its customers with consistently high quality products.
All employees are given comprehensive training on the requirements of the Quality System Regulation (QSR) and all aspects of Good Manufacturing Practices (GMP) prior to their first work assignment.
Our customers are encouraged to review The PMP Quality Manual and are invited to visit and conduct compliance audits. We will assist our customers with all of their regulatory requirements.