Suresh Anand Ph.D.,

Associate Professor at Rajalakshmi Engineering College
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Contact Information
us****@****om
(386) 825-5501
Location
Chennai, Tamil Nadu, India, IN
Languages
  • English Professional working proficiency
  • Tamil Native or bilingual proficiency

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Credentials

  • Master Medical Devices in Canada
    Udemy
    Dec, 2021
    - Oct, 2024
  • Awareness Program on Risk Management according to ISO 14971:2019 Standard
    TÜV SÜD
    Sep, 2021
    - Oct, 2024
  • Awareness on In-vitro Diagnostic Medical Devices Regulation (2017/746)
    TÜV SÜD
    Aug, 2021
    - Oct, 2024
  • Biocompatibility and Toxicological Assessment of Medical Devices – The Notified Body Perspective Training Assessment
    TÜV SÜD
    Aug, 2021
    - Oct, 2024
  • European Medical Device Regulation (2017/745)
    TÜV SÜD
    Jul, 2021
    - Oct, 2024
  • ISO 13485 Internal Auditor
    TÜV SÜD
    Jun, 2021
    - Oct, 2024
  • Mini-Course MDR 2017/745
    Easy Medical Device
    Oct, 2020
    - Oct, 2024
  • 10-reasons-get-use-orcid-id-certificate
    Elsevier
  • 8051 Microcontroller
    Bharath Acharya Academy
  • Book Writing
    Elsevier
  • Deep Learning
    PadhAI - One Fourth Labs
  • Detecting Image Manipulation Routines, Tools & Limitations
    Elsevier
  • Gender Bias in academic publishing
    Elsevier
  • How to get your book published
    Elsevier
  • Make the most of your research
    Elsevier
  • Why write a book
    Elsevier

Experience

  • Rajalakshmi Engineering College
    • India
    • Higher Education
    • 500 - 600 Employee
    • Associate Professor
      • Jun 2018 - Jul 2021

      -Research, Teaching, and Training Contributing to teaching and research including serving as a teacher, role model, and mentoring students, participate in the development and direction of research and educational program at the department level Complete evaluations for students and peers Applying the role of inter-disciplinary strategies combining engineering and biology to solve complex biomedical problems -Scholarly Activity Demonstrate effectiveness in securing grant… Show more -Research, Teaching, and Training Contributing to teaching and research including serving as a teacher, role model, and mentoring students, participate in the development and direction of research and educational program at the department level Complete evaluations for students and peers Applying the role of inter-disciplinary strategies combining engineering and biology to solve complex biomedical problems -Scholarly Activity Demonstrate effectiveness in securing grant funding of research initiatives and programs mentors and assist other faculty in grantsmanship Establishing an on-going commitment to and participating in scholarly activities at an advanced level as evidenced by publication of original research investigation, educational research, clinical observations, reviews, chapters, and books Applying innovative training in research methods to design and conduct clinical research on various areas of clinical specialty Fostering industry and clinical partnerships in healthcare needs Participate in collaborative research projects through interactions with researchers as well as individuals from other divisions & departments -Service and Administration Lead the integration of existing programs and development & growth of a major initiative of the assigned department and program Substantial leadership role in the direction of an academic division Participate as a member of the leadership team in developing consensus in the various programs, approaches, issues & new initiatives within the department Show less -Research, Teaching, and Training Contributing to teaching and research including serving as a teacher, role model, and mentoring students, participate in the development and direction of research and educational program at the department level Complete evaluations for students and peers Applying the role of inter-disciplinary strategies combining engineering and biology to solve complex biomedical problems -Scholarly Activity Demonstrate effectiveness in securing grant… Show more -Research, Teaching, and Training Contributing to teaching and research including serving as a teacher, role model, and mentoring students, participate in the development and direction of research and educational program at the department level Complete evaluations for students and peers Applying the role of inter-disciplinary strategies combining engineering and biology to solve complex biomedical problems -Scholarly Activity Demonstrate effectiveness in securing grant funding of research initiatives and programs mentors and assist other faculty in grantsmanship Establishing an on-going commitment to and participating in scholarly activities at an advanced level as evidenced by publication of original research investigation, educational research, clinical observations, reviews, chapters, and books Applying innovative training in research methods to design and conduct clinical research on various areas of clinical specialty Fostering industry and clinical partnerships in healthcare needs Participate in collaborative research projects through interactions with researchers as well as individuals from other divisions & departments -Service and Administration Lead the integration of existing programs and development & growth of a major initiative of the assigned department and program Substantial leadership role in the direction of an academic division Participate as a member of the leadership team in developing consensus in the various programs, approaches, issues & new initiatives within the department Show less

  • Biomedical Engineering
    • United States
    • Biotechnology
    • 1 - 100 Employee
    • Freelance Consultant
      • Jun 2017 - Jun 2018

      -Formulation of clinical protocols, methodologies and related documentation in collaboration with the multidisciplinary team including engineers and clinical doctors -Identify sites and manage study set-up -Support the study-related questions and serve as the point of contact for managing/ answering questions relating to trial procedures and subjects eligibility -Formulation of clinical protocols, methodologies and related documentation in collaboration with the multidisciplinary team including engineers and clinical doctors -Identify sites and manage study set-up -Support the study-related questions and serve as the point of contact for managing/ answering questions relating to trial procedures and subjects eligibility

  • School of Electrical Engineering, Amrita Vishwa Vidyapeetham
    • Adjunct Assistant Professor
      • May 2017 - May 2018

      Teaching courses in Fundamentals of Electrical and Electronics Engineering and Biomedical Instrumentation Disseminate and impart basic or applied knowledge to students Assist students with the learning process and applying the knowledge Teaching courses in Fundamentals of Electrical and Electronics Engineering and Biomedical Instrumentation Disseminate and impart basic or applied knowledge to students Assist students with the learning process and applying the knowledge

  • Center for Industrial Research and Innovation, Amrita Vishwa Vidyapeetham
    • Assistant Professor
      • May 2017 - May 2018

      Research in biomedical optics, with emphasis on clinical applications of optical spectroscopy and label-free tissue sensing in general To form close collaborations with clinicians, research centers and companies to accelerate biomedical optical technology and rapidly deliver this new technology into the hands of health-care providers Using photonics as a driver for the faster development and deployment of more accurate, minimally invasive diagnostic and treatment methods for… Show more Research in biomedical optics, with emphasis on clinical applications of optical spectroscopy and label-free tissue sensing in general To form close collaborations with clinicians, research centers and companies to accelerate biomedical optical technology and rapidly deliver this new technology into the hands of health-care providers Using photonics as a driver for the faster development and deployment of more accurate, minimally invasive diagnostic and treatment methods for cancer and other disease types Show less Research in biomedical optics, with emphasis on clinical applications of optical spectroscopy and label-free tissue sensing in general To form close collaborations with clinicians, research centers and companies to accelerate biomedical optical technology and rapidly deliver this new technology into the hands of health-care providers Using photonics as a driver for the faster development and deployment of more accurate, minimally invasive diagnostic and treatment methods for… Show more Research in biomedical optics, with emphasis on clinical applications of optical spectroscopy and label-free tissue sensing in general To form close collaborations with clinicians, research centers and companies to accelerate biomedical optical technology and rapidly deliver this new technology into the hands of health-care providers Using photonics as a driver for the faster development and deployment of more accurate, minimally invasive diagnostic and treatment methods for cancer and other disease types Show less

  • National Institute of Optics-National Research Council
    • Research Fellow
      • Feb 2016 - Feb 2017

      - Design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities as per ISO 13485:2016 and risk management assessment for medical devices as per ISO 14971:2012 - Verify for the general safety and performance requirement (GSPR), technical file, labeling, instruction for use (IFU), Unique Device Identification (UDI) system for medical devices comply as per new European Union Medical… Show more - Design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities as per ISO 13485:2016 and risk management assessment for medical devices as per ISO 14971:2012 - Verify for the general safety and performance requirement (GSPR), technical file, labeling, instruction for use (IFU), Unique Device Identification (UDI) system for medical devices comply as per new European Union Medical Device Regulations (EU-MDR) regulation - Evaluate and summarize clinical evidence including data from sources such as clinical investigations, scientific literature search, post-market surveillance (PMS), and post-market clinical follow-up (PMCF) - Research on requirements (local, national, international), applicable guidance and standards and options for regulatory submissions, approval pathways, and compliance activities - Collect and organize information on requirements for regulatory, quality, pre-clinical, and clinical data to meet applicable regulations - Key role in external and internal audits related to the product submission and notified body audit - Review and recommend changes for labeling, and clinical protocols to maintain regulatory compliance - Lead team to drive medical device product development for optical diagnosis of tumors and other areas of focus as applicable - Working in a cross-functional team of medical doctors, scientists, and engineers in addressing clinical problems and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from a global and/or regional perspective Show less - Design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities as per ISO 13485:2016 and risk management assessment for medical devices as per ISO 14971:2012 - Verify for the general safety and performance requirement (GSPR), technical file, labeling, instruction for use (IFU), Unique Device Identification (UDI) system for medical devices comply as per new European Union Medical… Show more - Design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities as per ISO 13485:2016 and risk management assessment for medical devices as per ISO 14971:2012 - Verify for the general safety and performance requirement (GSPR), technical file, labeling, instruction for use (IFU), Unique Device Identification (UDI) system for medical devices comply as per new European Union Medical Device Regulations (EU-MDR) regulation - Evaluate and summarize clinical evidence including data from sources such as clinical investigations, scientific literature search, post-market surveillance (PMS), and post-market clinical follow-up (PMCF) - Research on requirements (local, national, international), applicable guidance and standards and options for regulatory submissions, approval pathways, and compliance activities - Collect and organize information on requirements for regulatory, quality, pre-clinical, and clinical data to meet applicable regulations - Key role in external and internal audits related to the product submission and notified body audit - Review and recommend changes for labeling, and clinical protocols to maintain regulatory compliance - Lead team to drive medical device product development for optical diagnosis of tumors and other areas of focus as applicable - Working in a cross-functional team of medical doctors, scientists, and engineers in addressing clinical problems and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from a global and/or regional perspective Show less

  • Department of Physics and Astronomy, University of Florence
    • Research Associate
      • Feb 2015 - Jan 2016

      - Creating, reviewing, and updating technical documentation, product description, instruction for use (IFU), design and manufacturing information - Proven track record in building and managing a dynamic and high-performance medical writing team that is fit-for-purpose and resource-efficient - Responsible to plan, coordinate and conduct the execution of design protocols (eg. design validation and verification), testing reports, specifications, device master record (DMR), and design history… Show more - Creating, reviewing, and updating technical documentation, product description, instruction for use (IFU), design and manufacturing information - Proven track record in building and managing a dynamic and high-performance medical writing team that is fit-for-purpose and resource-efficient - Responsible to plan, coordinate and conduct the execution of design protocols (eg. design validation and verification), testing reports, specifications, device master record (DMR), and design history file (DHF) updates - Generate test protocols, analyze test data, and generate written reports - Verification and validation activities for new/replacement and existing products and components - Review of adequacy of product specification and support regulatory-related remediation that involves product design or functionality. - Utilize technical data and statistical analysis techniques such as measurement system analysis, process capability studies, and design of experiments (DoE) - Capability to interpret design and development related documents, functional and performance testing, biocompatibility, and risk analysis concerning safety regulations, quality policies, best practices, and procedures through training Show less - Creating, reviewing, and updating technical documentation, product description, instruction for use (IFU), design and manufacturing information - Proven track record in building and managing a dynamic and high-performance medical writing team that is fit-for-purpose and resource-efficient - Responsible to plan, coordinate and conduct the execution of design protocols (eg. design validation and verification), testing reports, specifications, device master record (DMR), and design history… Show more - Creating, reviewing, and updating technical documentation, product description, instruction for use (IFU), design and manufacturing information - Proven track record in building and managing a dynamic and high-performance medical writing team that is fit-for-purpose and resource-efficient - Responsible to plan, coordinate and conduct the execution of design protocols (eg. design validation and verification), testing reports, specifications, device master record (DMR), and design history file (DHF) updates - Generate test protocols, analyze test data, and generate written reports - Verification and validation activities for new/replacement and existing products and components - Review of adequacy of product specification and support regulatory-related remediation that involves product design or functionality. - Utilize technical data and statistical analysis techniques such as measurement system analysis, process capability studies, and design of experiments (DoE) - Capability to interpret design and development related documents, functional and performance testing, biocompatibility, and risk analysis concerning safety regulations, quality policies, best practices, and procedures through training Show less

  • European Laboratory for Non-Linear Spectroscopy
    • Italy
    • Research Services
    • 1 - 100 Employee
    • Postdoctoral Research Fellow
      • Jan 2013 - Jan 2015

      - Develop and translate an investigational device based on Trimodal spectroscopy for detecting brain tumor margins. This instrument was to be installed in the Department of Neurosurgery at the Anna Meyer Pediatric Hospital to conduct active clinical studies - Establish an investigational review board (IRB) to evaluate and monitor biomedical research involving human subjects for submission to the local regulatory authorities including the Department of Planning and Organization of the… Show more - Develop and translate an investigational device based on Trimodal spectroscopy for detecting brain tumor margins. This instrument was to be installed in the Department of Neurosurgery at the Anna Meyer Pediatric Hospital to conduct active clinical studies - Establish an investigational review board (IRB) to evaluate and monitor biomedical research involving human subjects for submission to the local regulatory authorities including the Department of Planning and Organization of the National Health Service, Italy, Food and Drug Administration (FDA) as a part of Code of Federal Regulations (CFR) - Support deployment of the quality management system (QMS) structure to ensure compliance to ISO 13485, 21 CFR 820, and European Regulations - Maintain, enforce, and manage compliant and effective QMS for the activities in scope, as well as for effective and lean QMS structures and documents for quality and regulatory (Q&R) processes at all levels - Report on key performance indicators (KPIs) to adhere to process and prevent the occurrence of any non-conformity relating to product, process, or system and data analysis using various statistical tools - Help in the filing and signing of quality documents including quality manuals, standard operating procedures (SOPs), work instructions, and related formats - Manage the review and approval process of clinical submissions documents, writing documents, generating consensus among reviewers, and facilitating discussions - Tracking medical device-related information utilizing databases, spreadsheets, and other tools Show less - Develop and translate an investigational device based on Trimodal spectroscopy for detecting brain tumor margins. This instrument was to be installed in the Department of Neurosurgery at the Anna Meyer Pediatric Hospital to conduct active clinical studies - Establish an investigational review board (IRB) to evaluate and monitor biomedical research involving human subjects for submission to the local regulatory authorities including the Department of Planning and Organization of the… Show more - Develop and translate an investigational device based on Trimodal spectroscopy for detecting brain tumor margins. This instrument was to be installed in the Department of Neurosurgery at the Anna Meyer Pediatric Hospital to conduct active clinical studies - Establish an investigational review board (IRB) to evaluate and monitor biomedical research involving human subjects for submission to the local regulatory authorities including the Department of Planning and Organization of the National Health Service, Italy, Food and Drug Administration (FDA) as a part of Code of Federal Regulations (CFR) - Support deployment of the quality management system (QMS) structure to ensure compliance to ISO 13485, 21 CFR 820, and European Regulations - Maintain, enforce, and manage compliant and effective QMS for the activities in scope, as well as for effective and lean QMS structures and documents for quality and regulatory (Q&R) processes at all levels - Report on key performance indicators (KPIs) to adhere to process and prevent the occurrence of any non-conformity relating to product, process, or system and data analysis using various statistical tools - Help in the filing and signing of quality documents including quality manuals, standard operating procedures (SOPs), work instructions, and related formats - Manage the review and approval process of clinical submissions documents, writing documents, generating consensus among reviewers, and facilitating discussions - Tracking medical device-related information utilizing databases, spreadsheets, and other tools Show less

  • Indian Institute of Technology Madras
    • India
    • Higher Education
    • 1 - 100 Employee
    • Graduate Research Assistant
      • Dec 2007 - Jan 2013

      - Applied diffuse reflectance spectroscopy for monitoring the wound healing process in diabetic foot ulcers and the effects of probe pressure on spectroscopic measurements - Literature search, analysis, and summarization of the relevant clinical data - Participate as the clinical representative for review and summarize of post-marketing surveillance data and risk analysis activity, complaint investigation - Collaborate with the project/program stakeholders for product knowledge and… Show more - Applied diffuse reflectance spectroscopy for monitoring the wound healing process in diabetic foot ulcers and the effects of probe pressure on spectroscopic measurements - Literature search, analysis, and summarization of the relevant clinical data - Participate as the clinical representative for review and summarize of post-marketing surveillance data and risk analysis activity, complaint investigation - Collaborate with the project/program stakeholders for product knowledge and information to develop quality content for the CER and within the required timelines - Understand clinical data from literature and clinical trials to ascertain safety and performance outcomes relevant to the device under evaluation Show less - Applied diffuse reflectance spectroscopy for monitoring the wound healing process in diabetic foot ulcers and the effects of probe pressure on spectroscopic measurements - Literature search, analysis, and summarization of the relevant clinical data - Participate as the clinical representative for review and summarize of post-marketing surveillance data and risk analysis activity, complaint investigation - Collaborate with the project/program stakeholders for product knowledge and… Show more - Applied diffuse reflectance spectroscopy for monitoring the wound healing process in diabetic foot ulcers and the effects of probe pressure on spectroscopic measurements - Literature search, analysis, and summarization of the relevant clinical data - Participate as the clinical representative for review and summarize of post-marketing surveillance data and risk analysis activity, complaint investigation - Collaborate with the project/program stakeholders for product knowledge and information to develop quality content for the CER and within the required timelines - Understand clinical data from literature and clinical trials to ascertain safety and performance outcomes relevant to the device under evaluation Show less

  • Johh F Welch Technology Center-GE Global Research
    • Interim Research Intern
      • Jul 2012 - Dec 2012

      Worked on various projects related to liquid crystals, imaging through turbid medium, surface plasmon resonance Worked on various projects related to liquid crystals, imaging through turbid medium, surface plasmon resonance

  • Medical Physics Lab, College of Engineering Guindy, Anna University
    • Research Assistant
      • May 2006 - Jul 2007

      Performed experiments for the differentiation of normal and malignant oral tissues using fluorescence, diffuse reflectance and synchronous luminescence spectroscopy. Identifying sensitivity and specificity diagnosis criteria for normal and malignant oral tissues. Development of physical tissue models for spectroscopic applications Performed experiments for the differentiation of normal and malignant oral tissues using fluorescence, diffuse reflectance and synchronous luminescence spectroscopy. Identifying sensitivity and specificity diagnosis criteria for normal and malignant oral tissues. Development of physical tissue models for spectroscopic applications

  • Tamil Nadu Government Dental College
    • Higher Education
    • 1 - 100 Employee
    • Intern
      • Sep 2006 - Apr 2007

      Collaborating with surgeons and pathologists for minimally invasive diagnosis of oral cancer Learnt various aspects of tissue pathology Collaborating with surgeons and pathologists for minimally invasive diagnosis of oral cancer Learnt various aspects of tissue pathology

  • Sykes Enterprises India Limited
    • India
    • 1 - 100 Employee
    • Technical Support Representative
      • Sep 2003 - Dec 2004

      Interact with customers to provide and process information in response to technical inquiries, concerns, and requests about products and services related to palm-One handhelds Follow standard processes and procedures Identify and escalate priority issues per client specifications Redirect problems to appropriate resource Interact with customers to provide and process information in response to technical inquiries, concerns, and requests about products and services related to palm-One handhelds Follow standard processes and procedures Identify and escalate priority issues per client specifications Redirect problems to appropriate resource

Education

  • Indian Institute of Technology Madras
    Doctor of Philosophy (PhD), Biomedical Optical Spectroscopy, Vascular dynamics during wound healing process
    2007 - 2013
  • College of Engineering Guindy, Chennai
    M.Tech, Laser Technology
    2005 - 2007
  • Bharathidasan University
    Bachelor of Engineering (B.Eng.), Electronics and Instrumentation Engineering
    1999 - 2003

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