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188金宝搏网站靠谱吗操纵子策略师医疗器械咨询c188金宝慱亚洲体育ompanies which provides regulatory 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 the clients customized solutions to manufacturers looking to set up a world-class manufacturing unit.

Our global presence caters to clients from around the globe & includes small start-ups to world’s renowned medical device manufacturers. We have a team of experts whose knowledge & experience helps them handle clients both small & large.

Our Services

FDA 510 k Clearance

We are a Bunch of Regulatory Professionals & Experts in FDA 510 k clearance

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When it comes to CDSCO medical device license process, Operon strategist makes the lengthy process easy and smooth.

Medical Device CE Mark

We help you in the process of making a defined and comprehensive technical file with all product details required for CE marking.

TURNKEY PROJECT CONSULTANT

We provide medical device regulatory consulting services for Turnkey Project that includes Facility layout design, Regulatory support for Clean Room,…

MEDICAL DEVICE CONSULTING SERVICES

ISO 13485 Consultant provides Guidance for medical device manufacturers for obtaining ISO 13485 certification Quality Management System

PRIMARY PACKAGING CONSULTANT SERVICES

Combination Product approval from FDA. Drug Device Combination Products is the combination of two or more drugs and medical device. ISO 13485:2016

MEDICAL DEVICE COMBINATION PRODUCTS

With the expertise in regulatory affairs and quality management systems, we monitor facilities…

Medical Device Design and Development

Medical Device Design and Development plays a vital role in making the medical device. This is the most important stage in the medical device development

21 cfr part 820 (QSR)

FDA 21 CFR Part 820 Quality System Regulation Consultant Services For Medical Device Manufacturers.

Design Control Requirements

US FDA 21 CFR 820.30 Design Control Requirements for medical device design. Design Control Guidance For Medical Device Manufacturers

Operon Strategist is an expert Medical Device manufacturing consultancy providing registration support for Medical Equipment manufacturing in India.

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For Inquiries - FDA, CDSCO And CE.

Our Valuable Clients

Our Valuable Clients

“Operon Strategist is an outstanding medical device consulting firms with whom I will do business again and these are my reasons.

A true problem solver Very Reliable”

Zak Kouloughi - President

Tradeline Medical Lab, USA

“We hired Operon Strategist the medical device consultant as a subject matter expert for overseeing the sterilization activity by adhering to the protocol and for reviewing results and reports in like with global standards and our requirements for the commercial launch of a product in the global market.”

Rahul Paith - Project Manager

Medtronic, India

“We have had good experience working with OperonStrategist the Medical Device Consultant, The team is experienced, Knowledgeable, result oriented, committed and professional in training and execution of the project, We strongly recommend Operon Strategist for all the services”

Arun Kumar - Director

MP Qatar Trading, Qatar
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