Sterilization, Sanitation and Disinfection in the Hospital


Download Sterilization, Sanitation and Disinfection in the Hospital


Preview text

7 February 2020
Ebro Webinar:
Sterilization, Sanitation and Disinfection in the Hospital /
Medical Industry

Two Key Requirements in the Hospitals and CSSD:
1. Washing and Disinfection
You Cannot Sterilize What You Cannot Clean (Contaminated Materials)
2. Sterilization
Reduction of Microbial / Bacterial Spores (Sterile Goods)

Your Xylem Analytics Colleagues and Friends wishing everyone and your families all the best and good health amidst the current COVID19 pandemic
“Life nowadays is not mereley being Alive, but being Well”

Who is Xylem? We are one of the world's leading water technology companies
4

2017 Revenue Employees Countries Continents

$4.7bn 16,500 150 7

Bringing together the most progressive brands

Transport

Treatment

Dewatering

Applied Water Solutions
Specialty Flow Control

Measurement & Control Solutions

Analytics

Advanced Infrastructure
Analytics

5

Xylem Analytics Breakdown

Process
~30%

Laboratory
~25%

Ocean
~10%

Surface
~35%

6

The Hospital **CSSD Workflow
-Washer + Disinfectors

BULK SUPPLY
General Store
Clean Receipt

Instruments Gloves

Wards & Units
Dirty Receipt
OPERATING THEATER PATIENT ROOMS

Disassembly Rubberwares

Cotton, Gauze, etc.

** CSSD: Central Sterile Services Department

Assembly
Inspection Pre-Sterile Storage
Sterilization Sterile Storage
Distribution

The Hospital CSSD Workflow: “Where we can provide the solutions” Cleaning and Disinfection - Reusable MedicalToolds / Equipment
- Stainless Steel Surgical and Operation instrumentations - Catheters, IV pumps and crash carts - Main Target: Endoscopes and other contaminations
Sterilization
- Especially for “Critical Items” such as any instruments which are introduced into a human blood stream - Main Target: All living and active organisms /
Microorganisms

7 February 2020
• Regulation: Standards and Norms
Standards
- Law of Medical Products - Medical Products Operator Ordinance Social Law - Hygiene requirements for conditioning medical products“
The validation of processes in the conditioning of medical products is legally binding.

VALIDATION
The essentials of Validation: The Installation Qualification (IQ), the Operation Qualification (OQ) and the Performance Qualification (PQ).
Validation is a complete presentation and verification of facts, that procedures, processes, equipment, materials, process steps or systems actually lead to the expected results.
The results are then summarized and presented in details in a validation report, which helps to evaluate and assess the predetermined acceptance criteria and process optimization objectives

Preparing to load PDF file. please wait...

0 of 0
100%
Sterilization, Sanitation and Disinfection in the Hospital