- STORE
- >
- ISO 13485 QUALITY SYSTEM PROCEDURES
- >
- ISO 13485 PRODUCT REALIZATION PROCEDURES
- >
- ISO 13485 PURCHASING PROCEDURES
- >
- Purchase Order Procedure | ISO 13485
Purchase Order Procedure | ISO 13485
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- MS Word Format
- Includes Applicable Form
- Instant Download - Digital Content
Purchase Order ProcedureThe ISO 13485 Purchase Order Procedure establishes the process for purchasing materials, products or services and the methods utilized to maintain purchasing data.
Purchase Order Procedure - OverviewThe Purchase Order Procedure applies to all purchase orders placed by the Purchasing Department. The procedure provides instruction for verifying supplier approval status, the required content for purchase orders, and the required notice to suppliers for notification of any change in product or processes.
Purchase Order Procedure - ComplianceThe Purchase Order Procedure is ISO 13485:2016 and FDA 21 CFR Part 820 compliant.
For more information about our Purchase Order Procedure contact us at [email protected]
RELATED LINKS |
|
Customer's also viewed
Supplier Management Procedure | ISO 13485 | FDA QSR Compliant
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- Includes Related Forms
- MS Word Format
- Digital Content - Instant Download
ISO 13485 Contract Review Procedure
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- MS Word Format
- Instant Download Digital Content
Medical Device Quality Management System | MANUFACTURING
The Medical Device Quality Management System | MANUFACTURING product is designed for companies engaged in both product development and the manufacture of medical devices. The system is rich in content and provides detailed instruction governing research and development, manufacturing and post commercialization activities. The system is configured for companies desiring ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!
- Quality Management System Manual
- 60 Procedures and Related Forms (MS Word and Excel)
- ISO 13485:2016 and FDA QSR Compliant
- MDR EU 2017/745 Compliant
- Digital Content - Instant Download
Medical Device Quality Management System | MANUFACTURING PLUS
The Medical Device Quality Management System | MANUFACTURING PLUS System is our "top line" QMS product configured for companies engaged in the design and manufacture of medical devices seeking ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!
- Quality Management System Manual
- 72 Procedures and Related Forms (MS Word and Excel)
- ISO 13485:2016 and FDA QSR Compliant
- MDR EU 2017/745 Compliant
- Digital Content - Instant Download