- STORE
- >
- ISO 13485 QUALITY SYSTEM PROCEDURES
- >
- ISO 13485 PRODUCT REALIZATION PROCEDURES
- >
- ISO 13485 PRODUCTION SERVICE PROVISION PROCEDURES
- >
- Respiratory Protection Procedure
Respiratory Protection Procedure
- ANSI Z88.2-2015 Compliant
- OSHA 29 CFR 1910.134 Compliant
- ISO 13485 Compliant
- FDA QSR Compliant
- MS Word Format
- Digital Content - Instant Download
Respiratory Protection ProcedureThe Respiratory Protection Procedure assures the safe and proper use of respirators by employees at the company, and to maintain compliance with the Occupational Safety & Health Administration's (OSHA) regulations as described in 29 CFR 1910.134 Respiratory Protection.
Respiratory Protection Procedure - OverviewThe Respiratory Protection Procedure governs the respiratory protection requirements, as specified in 29 CFR 1910.134 (Respiratory Protection), in the control of occupational diseases caused by breathing air contaminated with harmful dusts, fogs, fumes, mists, gases, smokes, sprays, or vapors, the primary objective shall be to prevent atmospheric contamination.
Respiratory Protection Procedure - ComplianceThe Respiratory Protection Procedure complies with ANSI Z88.2-2015, OSHA 29 CFR 1910.134, ISO 13485:2016 and FDA QSR.
For more information about our respiratory protection procedure contact us at [email protected]
RELATED LINKS |
Respiratory Protection Preview |
Customer's also viewed
Medical Device Quality Management System | BASE PLUS SYSTEM
The Medical Device Quality Management System | BASE PLUS is configured for companies engaged in the design and manufacture of medical devices who need only the minimum required content to obtain ISO 13485:2016 certification and FDA QSR compliance. Products installed in 46 countries and growing!
- Quality Management System Manual
- 38 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 | DESIGN PLUS
The DESIGN PLUS Quality Management System (QMS) is configured for companies engaged in research and development of medical devices but perform no manufacturing (Specification Developers). The Design Plus QMS 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
- 46 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
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