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08:10
Annex-2 (IVD) of SFDA Medical Device Registration Process|Saudi Food & Drug Authority L-5
10:18
Annex-1 ( MD) of SFDA Medical Device Registration Process|Saudi Food & Drug Authority L-4
06:39
Process Flow Chart for SFDA Medical Device Registration Process|Saudi Food & Drug Authority L-3
16:23
Root Cause Analysis (RCA) for ISO 13485 Nonconformities | 5 Why Analysis | Fish Bone Diagram|CAPA !!
00:26
Material Handling in Daily Operations| Machine for Handling of Goods in WareHouse & Logistic Area
04:15
ISO 13485:2016 Medical Device -QMS|Clause 8.1 Measurement , analysis and improvement |L-13
18:21
MOHAP Portal Navigation: A Beginner's Guide|Navigating with Ease|Unlock Step-by-Step Tutorial U.A.E
02:31
Unlocking Sri Lanka's Medical Device Registeration Requirements in 2 Minutes @ivdmanufacturing7208
08:31
ISO 13485:2016 Medical Device -QMS|Clause 7.6 Control of monitoring and measuring equipment |L-12
21:23
Product Registeration in United Arab Emirates | Medical Device and IVD Registeration in U.A.E| MoHAP
10:40
ISO 13485:2016 Medical Device -QMS|Clause 7.4 Purchasing |L-10|Purchase or Procurement Department
20:17
ISO 13485:2016 Medical Device -QMS|Clause 7.3 Design and Development |L-9| Research and Development
11:54
ISO 13485:2016 Medical Device -QMS|Clause 7.2 Customer Related Process |L-8| Customers , End User
07:11
FSCA| Filed Safety Corrective Action Form India CDSCO MDR 2017| How to fill FSCA Forms for Complaint
06:48
ISO 13485:2016 Medical Device -QMS|Clause 7.1 Planning of Product Realization |L-7| Operations Only
16:20
Medical Device Adverse Event Form - Indian CDSCO MDR 2017 | What is MDAE | Adverse Event Reporting
19:19
ISO 13485:2016 Medical Device -QMS|Clause 6 Resource Management |L-6| Human Resource Department !!
00:52
Why do Employees Quietly Quit Job Know the Reason in Just 52 Seconds !!!!!
22:09
ISO 13485:2016 Medical Device -QMS|Clause 5 Management Responsibility |L-5 @ivdmanufacturing7208
15:35
Medical Device and IVD Process Validation | Basic of Process Validation| Conduct Process Validation
18:53
ISO 13485:2016 Medical Device -QMS|Clause 4 Quality Management System (QMS) for Medical Devices |L-4
02:27
Automatic Lyophilizer Machine for RT PCR Master Mix | IVD Equipment | Lyophilization Process in IVD
17:36
ISO 13485:2016 Medical Device- QMS | Clause 3 Terms & Definitions| Standard for Medical Devices |L-3
03:33
ISO 13485:2016 Medical Device- QMS | Clause 2 Normative Reference| Standard for Medical Devices |L-2
08:12
ISO 13485:2016 Medical Device- QMS | Clause 1 Scope| Standard for Medical Devices & IVD | Lecture-1
16:16
Medical Device Risk Analysis & Periodic Review|Risk Management Plan|ISO14971:2019 Risk Standards|IVD
17:31
510(k) Clearances-FDA|Premarket Notifications 510(k)|510(k) Submission Process|Medical Device Entry
00:20
Bio Dot Reagent Dispenser Machine for Flow Through Assay Manufacturing |HCV Bi Dot HIV Tri-Dot Test
03:32
Required Document for SFDA Medical Device Registration Process|Saudi Food & Drug Authority L-2
04:04
US FDA Medical Device Registration Process Overview| US FDA Regulatory Pathway & Classification
09:11
SFDA Medical Device Registeration Process| SFDA Application Process| Saudi Food & Drug Authority L-1
12:38
Manufacturing Process of Rapid Uncut Sheet HBsAg,HIV1/2,HCV,Pregnancy Kit @ivdmanufacturing7208
19:56
CDSCO Import License Application Process for Medical Devices|MD Form|How to File Import License|NSWS
12:45
Quality Control Procedure as per ISO13485:2016 | Quality Control Implementation ISO13485:2016|IVD|QC
02:14
Iso Flow Reel to Reel Reagent Dispenser Machine for Lateral Flow Assay Manufacturing | IVD Test Kits
02:44
In Vitro Diagnostic Medical Device News|Indian CDSCO News| Indian Regulatory Updates[April 2024]✓✓
02:08
In Vitro Diagnostic Medical Device News|Indian CDSCO News| Indian Regulatory Updates[March 2024]✓✓
08:43
Quick Steps to Launch Medical devices into the Indian Market|Indian CDSCO MDR-2017|Class A ,B,C&D !!
08:32
How IVD Manufacturer respond against PMS or Customer Feedback |Lecture-4|Post Market Surveillance!
10:08
Stakeholder Roles & Responsibilities in Post Market Surveillance|Manufacturer|(L-3)
11:50
Stakeholder Roles & Responsibilities in Post Market Surveillance| End User|Procurer|Patients(L-2)
16:28
Medical Device under Post Market Surveillance|Quick Insight on Post Market Surveillance (L-1)
05:57
Calculate Accelerated Aging Time via Simple Calculator| Accelerated Aging Time for Medical Device
08:45
Factory Set Up for Medical Device & IVD | Plant Set Up for Medical Device in just 10 Minutes! Secret
04:47
Overview of Performance Studies for an IVDs | Analytical & Clinical Studies|@ivdmanufacturing7208
02:38
In Vitro Diagnostic Medical Device News|Indian CDSCO News| Indian Regulatory Updates[February2024]✓✓
02:18
In Vitro Diagnostic Medical Device News|Indian CDSCO News| Indian Regulatory Updates[January 2024]✓✓
04:26
WHO-PQ IVD Product List | All you should know about this | Bench Mark Manufacturer for New Entrants!
14:19
How to apply central approvals on NSWS | File Test License Application Form in Just 10 Minutes CDSCO
12:09
How to register, sign in, create business profile on NSWS|National Single Window System-India| CDSCO
07:46
EU Regulation Medical Device | IVDD | Directive 98/79 EC | What is EU MDR 2017 | IVDR | Lecture-2
07:14
ISO 11737-1:2018 Standard|Sterilization of Medical Device Product| What is ISO 11737-1 Standard?L-2!
12:10
ISO 11737-1:2018 Standard|Sterilization of Medical Device Product| What is ISO 11737-1 Standard? L-1
11:02
Medical Device Sterilization |Guide to Sterilization Process| Sterile and Non-Sterile Medical Device
01:58
Basic Molecular Biology: PCR and Real-Time PCR – Principle of PCR|Real Time PCR| Molecular Technique
04:46
How to get ISO13485 MD-QMS Certificate|Selection of Notified Bodies|ISO Certificate for Manufacturer
26:32
Steps to fill the License Application Form on CDSCO Online Portal|MD Form Filling|MDR,2017|IVD|:L-3
06:08
How to operate an Online System for Medical Device CDSCO|Medical Device Registration in India:L-2
09:32
How to operate an Online System for Medical Device CDSCO|Registration of Medical Device in India:L-1
03:39
Rapid Diagnostic Tests (RDTs): Principle, Schematic 3D Diagram, Parts|Lateral Flow Assay|IVD KITS!!!
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