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Operon Strategist @[email protected]

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00:26
Operon Strategist's Silver Partnership: 7th Annual Medical Device Regulatory and Quality Summit 2023
02:56
CE or US FDA 510(k): What Should You Choose for Your Medical Device?
07:42
EU MDR Transition extension : A complete Guide for Medical Devices
00:51
Class C&D Medical Devices registration in India: CDSCO Registration
00:31
Register your Medical Device in CDSCO India.🩺
00:22
Design & Development Documentation for Medical Device
00:24
Major Benefits of ISO 13485 QMS for Medical Devices | Operon Strategist
00:20
How to get your CE Mark Certification for Medical Devices ?
00:20
Drug Device Combination products certificate for medical devices
00:19
Best Turnkey Project Consultant For Medical Devices
01:11
UKCA Marking for medical Devices
04:01
Registration Certificate for the Sale or Distribution of Medical Devices
00:30
CDSCO Notification for Class A Non-sterile and Non measuring Medical Device
05:32
CDSCO Notification for Class A Non-sterile and Non measuring medical devices
00:32
( SFDA) Saudi Arabia FDA Medical Device Registration Process.
00:31
Challenges to import medical devices in India
01:50
Challenges for importing Medical Device in India
01:09
How to start manufacturing medical devices
00:31
Newsletter for Medical Device Regulatory updates - "Reguveda"
00:31
Operon Strategist | Medical Device Regulatory Consultant
00:31
Turnkey Project Consultant For Medical Devices
00:16
US FDA 510(k) Clearance & Premarket approval-Operon Strategist
00:16
CDSCO Import License consultant for medical device
00:59
CDSCO Import License for Medical Devices-Operon Strategist
00:16
Turnkey Project Consultant For Medical Devices
01:08
How to start Medical Device Manufacturing | Operon Strategist
01:25
What is MDSAP And Why is it required?
00:44
FDA 510 k Clearance & Premarket Approval
00:49
Best Turnkey Project Consultant For Medical Devices
01:50
Medical Device Manufacturing Consultants | Operon Strategist
00:58
Online Certification Courses for Medical Devices - Operon Strategist
00:54
CDSCO Registration For Wholesale and Manufacturing License
00:38
Voluntary Registration of Medical Devices - Operon Strategist
02:31
Design History File Consultant - Operon Strategist
07:21
What is European Medical Device Regulation (EU MDR)?
03:25
FDA 510 (k) Approval Services On Medical Device - Operon Strategist
05:30
Medical Device Regulatory Consulting Services - Operon Strategist
00:36
Online Certification Courses for Medical Devices - Quality & Regulatory Affairs
00:48
What is ISO 15378 Certification for medical devices
00:59
Regulatory Clean Room Requirement Consultants - Operon Strategist
01:38
How to start medical device manufacturing?
02:48
ISO 13485 Consultant - Operon Strategist
01:06
what is a drug master file?
01:15
How To Get Medical Device Registered in India?
01:04
What is Medical Device Process Validation? | Operon Strategist
01:19
What is MDSAP And Why is it required?
01:36
Medical Device Directive (MDD) to Medical Device Regulation (MDR)
01:29
CDSCO Import License for Medical Devices
01:02
QMS Certification Training for Medical Devices
00:59
Operon Strategist Provides Turnkey Project Consultants Services
00:51
CE Marking Certification Consultants Services | Operon Strategist
01:01
Wholesale and Manufacturing License | CDSCO Registration - Operon Strategist
00:53
FDA 510(k) Submission Consultation and Approval By operon strategist
03:00
Process Validation and Verification for Medical Device | Equipment Validation
03:00
Turnkey Project Consultants | Medical Device | Primary Packaging
02:15
ISO 15378 Quality Management System For Primary Packaging Material
02:15
Clean Room Design | ISO 14644 | Clean Room Regulation
00:36
FDA 21 CFR Part 820 Quality System Regulation
00:36
ISO 13485 Consulting | ISO 13485 Certification For Medical Device
00:50
Medical Device Design and Development | Combination Products | Design Control