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Malesh  M

Malesh M

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Personal Information
Organization / Workplace
Bangalore India
Occupation
Regulatory Consultant
Industry
Medical / Health Care / Pharmaceuticals
Website
maleshblog.wordpress.com/
About
Professional Qualification – B-Pharm (2011) Internal Auditor for ISO 13485 (Medical Device) Good understanding of ISO 13485, 21 CFR 820, Medical Device CE Marking, Schedule M, cGMP & FDA 510K.
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Presentations

(10)
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Medical device clinical evaluation

12 years ago • 3030 Views

Ce marking of catheters

11 years ago • 368 Views

Medical device labeling

11 years ago • 1420 Views

Iso 13485

11 years ago • 783 Views

Ce marking of sutures

11 years ago • 694 Views

Ce marking of mesh

11 years ago • 410 Views

Design and development of medical device

11 years ago • 2930 Views

Batch release certificate for medical device

11 years ago • 2355 Views

Technical file for Intraocular Lens

11 years ago • 703 Views

Technical file for ophthalmic microsurgical knives

11 years ago • 844 Views

Likes

(2)

Cross contamination in Pharmaceuticals - by Jitendra J Jagtap

jitendrajagtap1986 • 12 years ago

Clean room

I3CGLOBAL • 12 years ago
Personal Information
Organization / Workplace
Bangalore India
Occupation
Regulatory Consultant
Industry
Medical / Health Care / Pharmaceuticals
Website
maleshblog.wordpress.com/
About
Professional Qualification – B-Pharm (2011) Internal Auditor for ISO 13485 (Medical Device) Good understanding of ISO 13485, 21 CFR 820, Medical Device CE Marking, Schedule M, cGMP & FDA 510K.

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