Operon Strategist is a medical device regulatory consulting company which provides regulatory advisory & guidance to various manufacturers in the healthcare industry to ensure the strategic development of these manufacturers. We serve our clients by providing turnkey services, system implementation, training, licensing, regulatory approvals and certifications. We provide a complete turnkey solution to manufacturers looking to set up a world-class manufacturing unit. We also provide customized packages as per the requirements of the client. Our global presence caters to clients from around the globe & includes small start-ups to the world’s renowned medical device manufacturers. We have a team of experts whose knowledge & experience helps them handle clients both small & large. As a trusted partner to our clients, we strive to provide services within budget, agreed on timeline & to the highest quality standards in order to exceed expectations.
Operon Strategist is owned & partnered with world’s competent companies & renowned personalities in the field of medical device regulatory consulting. With more than 60+ cumulative years of experience, providing 1000+ services in the field of medical device regulatory consulting, Operon Strategist’s strategic alliance with these companies helps the clients in obtaining an insight into the regulations of various countries.
Healthcare industry is steadily growing both in India as well as internationally which can be attributed to raising awareness among people of various healthcare options & people being more open to spending on quality healthcare services. To ensure that safe & effective products reach the end consumer, manufacturers must ensure that they have an efficient manufacturing unit site equipped with a well-organized quality system & skilled workforce. Operon Strategist guides such manufacturers in various aspects of regulatory requirements.
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Contact details –
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
Phone no - 93702 83428
Mail id – enquiry@operonstrategist.com
If You Want Medical Devices Services Consultation For Following.- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
If You Want Medical Devices Services Consultation For Following.
- Medical Device Consulting
- cdsco registration
- FDA 510k Clearance
- ce mark medical device
- CDSCO Manufacturing License
- CDSCO import license
- TURNKEY PROJECT CONSULTANT
- medical device manufacturing
- iso 15378 certification
- 21 cfr part 210 and 211
- ISO 13485 Medical Device Consultant
- Primary Packaging Turnkey Project Consultant
- Clean Room Design Consultant
- manufacturing site conceptualization
- Market Analysis and feasibility for Medical Devices
- manufacturing plant layout design
- medical device design and development
- DMF file submission guideline
- 21 cfr part 820
- qms certification services
- capa management
- design control requirements
- medical device process validation
- combination product
- continuous improvement program
- Medical Device Compliance & Regulatory Services
- Cdsco India authorized agent for medical device
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