Operon Strategist provide consultancy For Clean Room Design

As a Clean Room Design consultants, we provide expertise clean room design solution to medical device manufacturers. Clean Room helps in establishing & maintaining an environment with a low level of environmental pollutants such as dust, airborne microbes, aerosol particles & chemical vapors. Clean Room is the facility ordinarily utilized as a part of specialized industrial production or scientific research. For that, clean room design is under the expertise is more important.

Clean Room Design Consultant

Presence of unwanted air particles may adversely affect the performance and safety of a product and hence Medical Device

manufacturers are advised to manufacture under classified areas. Clean rooms of different sizes and complexity are designed to maintain low levels of air particles as per the ISO 13485, ISO 14644 Clean Room Design Standards. Presence of unwanted air particles may adversely affect the performance and safety of a product and hence Medical Device manufacturers are advised to manufacture under classified areas. Clean rooms of different sizes and complexity are designed to maintain low levels of air particles as per the ISO 13485, ISO 14644 Clean Room Design Standards.

Read More - Clean Room Design Consultant

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Contact details –

Phone  no -  93702 83428

Mail id – enquiry@operonstrategist.com

If  You Want Medical Devices Services Consultation For Following.

1. Medical Device Consulting 
2. cdsco registration 
3. FDA 510k Clearance 
4. ce mark medical device 
5. CDSCO Manufacturing License 
6. CDSCO import license 
7. TURNKEY PROJECT CONSULTANT 
8. medical device manufacturing 
9. iso 15378 certification 
10. 21 cfr part 210 and 211 
11. ISO 13485 Medical Device Consultant 
12. Primary Packaging Turnkey Project Consultant 
13. Clean Room Design Consultant 
14. manufacturing site conceptualization 
15. Market Analysis and feasibility for Medical Devices 
16. manufacturing plant layout design 
17. medical device design and development 
18. DMF file submission guideline 
19. 21 cfr part 820 
20. qms certification services 
21. capa management 
22. design control requirements 
23. medical device process validation 
24. combination product 
25. continuous improvement program 
26. Medical Device Compliance & Regulatory Services 
27. Cdsco India authorized agent for medical device