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Medical Device Systems vs. Procedure Packs: What's the Difference?

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Quality Assurance_Ensuring documentation and system compliances

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Are you a Distributor or a Private Label Manufacturer under the EU MDR

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Unlock Global Markets: Simplify Your QMS with MDSAP Certification

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How do we manage your Quality and Regulatory Compliance?

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Medical Device Software (MDSW) intended to work in combination with hardware

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Scientific Validity Report Writing

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RegAQs - Frequently Asked Questions on the MDSAP process.

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Regulatory consultation process | Medical Device Regulatory Consultant | Regulatory affairs

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Common Specifications for IVD Manufacturers

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Regulatory affairs trainings

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Regulatory affairs updates - Guardians of compliance

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Relationship between Maven and our clients

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Unable to close NC raised during Audits? Maven has the solution

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How Maven Helps in Maintaining QMS Documentation

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Periodic Safety Update Report (PSUR)

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Maven Regulatory Services Introductory Deck

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Maven introduces the AMC Department for hassle-free regulatory and QMS management!

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MAVEN: 2022-23 Annual Report

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Maven - Chapter 2.0

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Maven Magazine 2021 - 22

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Testimonial - Ortho Max Mfg' Co' Pvt' Ltd'

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Testimonial from RFB LATEX LIMITED

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Gap Analysis (MDD to MDR, IVDD to IVDR, QMS, Standards)

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European Database for Medical Devices (EUDAMED) Registration

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The National Institute for Occupational Safety and Health (NIOSH Certification)

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Medical Devices Country Registration as per Country Regulatory Requirements

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Clinical Evaluation Report as per MEDDEV 2.7.1 Rev. 4

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CE Certification Consultancy for Medical Devices -Maven

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Unique Device Identification - Medical Devices

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Why Medical Device Liability Insurance is mandatory?

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Demonstration of Equivalence- Clinical Evaluation Report

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Training on mandatory requirements due to enforcement of EU MDR

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CE Marking Post Brexit - Using the UKCA marking

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What “State of the Art” really means in the EU MDR ?

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ETO validation - Sterlization Validation Process

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Types of Sterilization & Generic Steps for Validation of the Medical Device

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Person Responsible for Regulatory Compliance in EU MDR (PRRC)

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Maven Masterclass: Training on Key Changes: EU MDD to EU MDR

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Indian MDR for Medical Device Manufacturers/CDSCO - Central Drug Standard Control Organization

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Clinical Evaluation Process as per MDR article 61

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What is the significance of Labelling in Medical Device?

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Announcing Training on KEY CHANGES from EU MDD to EU MDR

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Want to export your Medical Devices in more than 100 Countries? CE Mark can help!

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Are you looking for a Medical Device Regulatory Consultant??

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Who is an EAR? (European Authorized Representative) Learn with Maven's latest video !

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What is PMCF Report? Mandatory Content Explained

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CE Marking Process as per EU MDR (European Medical Device Regulation)

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What is the change in PMS as per MDR 2017/745 ?? it is PSUR (Periodic Safety Update Report) report

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Medical Device Classification as per different Regulations

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MDD Essential Safety Requirements vs MDR General Safety & Performance Requirements

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Medical Device Single Audit Program (MDSAP)

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Economic Operators

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Maven Introduction from the Director

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Regulatory Strategy MD & IVD

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SSCP - Summary of safety and clinical performance

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Changes in Risk Management for Medical Devices - ISO 14971:2007 v/s ISO 14971:2019

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MDR vs MDD : 13 Key Changes