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1) ValidationasperNationalAccreditationBoardforHospitals&Healthcare(NABH)Guidelines
a) Air Par�cle Count Test
Spectro offers extensive airborne par�cle count cleanliness classifica�on. It is used to find out the par�cle count
level at the �me of tes�ng within a facility.
a) DOP Test/ HEPA Filter Integrity Test
Spectro conducts complete HEPA/ULPA filter integrity tests assuring the
filters are in conformance with several standards and/or government agency
requirements. Complete documenta�on & cer�fica�on is provided by us
which helps predict poten�al performance and enhances filter life.
c) Air Velocity Measurement
Spectro conducts Air Velocity Measurement/ tests to determine the average filter face uniformity & velocity
and the average room airflow velocity and uniformity within a clean room.
d) Temperature/ Humidity
Depending upon the requirement, there are 2 levels for conduc�ng Temperature and Humidity tests. In the first
level; general temperature & humidity uniformity are checked which ensures that the clean room's HVAC
system is maintaining the specified levels of temperature & humidity desired for comfort. While the second level
is a comprehensive level to iden�fy the clean room HVAC systems are maintaining the specified levels of
temperature & humidity necessary for both comfort and process temperature control.
e) Air changes per Hour
It determines how many �mes the air enters and exits a room from the HVAC system in an hour, by which we can
design or balance the airflow.
Air Changes/hr - CFM x 60 min
Volume of Room
f) Pressure Differen�al Test
This test verifies the pressure differen�al meet the specified requirements. A clean room may consist of mul�ple
rooms with different cleanliness requirement and thus the facility should be maintained at sta�c pressures
higher than atmospheric to prevent infiltra�on by wind.
Specialized Services for Hospitals
Specialized Services for Hospitals
Mechanical
· Vibra�on Machine or Objects
· Weighing Machine
· Pressure gauge/Digital pressure gauge
4) Thermal Valida�on
Thermal valida�on is the process of valida�ng/qualifying
equipment and storage facili�es to prove that they will create
and maintain the temperatures they are designed for.
5) Water Tes�ng as per IS 10500
Chemical, Physical & Microbiological tes�ng
6) EndotoxinTestingofDialysisWater
Waterusedfordialysishasstrictrequirementsonthelevelsof
chemical and biological contaminants allowed. Our testing
methodprovidesyouwithexactendotoxinlevels.
7) ETP/STPTesting
Hospitalsaresigni�icantconsumersofwaterandgenerateaconsiderableamountofwastewaterwhichconsists
ofharmfulpathogens,bacteria&virus,radioactivematerials,drugs,clinicaldischarges,domestic&suspended
solids,etc.
3) Calibra�on
Thermal
· Autoclaves
· Cold Rooms
· Incubators
· Ovens
· Refrigerators, Control Rate Freezers and Ultra Low Freezers
· Stability Chambers
· Warehouse Storage Facili�es
2) Medicalgas/CompressedgasTesting
Tomeetthespeci�icationforpipingpurity(Air,O ,N O,N ),pipingparticulate,veri�ierpipingpurity,medicalgas2 2 2
concentration(O ,N O,N )andmedicalairpuritytesting.2 2 2
Ü Metals & Alloys
Ü Non Destructive Testing
Ü Rubber & Polymers
Ü Food and Agro Products
Ü Coal, Solid Fuels & Petroleum
Ü Electrical & Electronics
Ü Pharmaceuticals & Drugs
Ü Building Materials
Ü Minerals & Chemicals
Ü Leather & Textiles
Ü Water & Environment
Ü Paper & Packaging Materials
Ü Hazardous Substances
Ü Clean Room Validation
E-41 Okhla Industrial Area Phase-IINew Delhi-110020Ph:- 91 11 40522000, 41611000E-mail: [email protected]:- www.spectrogroup.com www.spectro.in
Head Office Corporate Office
S-1 GNEPIP, Surajpur Industrial AreaKasna, Greater Noida, Phase-V
Gautam Budha Nagar (U.P.)Pin Code: 201308
Ph:- 0120-2341251/52 E-mail:- [email protected]
URL:- www.spectrogroup.com2017
Major Ac�vi�es
R&D
Automation
Reverse Engineering
Testing
Calibration
Training
Inspection
CIN : U74220DL1998PL C092698