Medical Device Guidelines and Regulations Handbook (eBook)

eBook Download: PDF
2022 | 1. Auflage
VI, 385 Seiten
Springer-Verlag
978-3-030-91855-2 (ISBN)

Lese- und Medienproben

Medical Device Guidelines and Regulations Handbook -
Systemvoraussetzungen
96,29 inkl. MwSt
  • Download sofort lieferbar
  • Zahlungsarten anzeigen

This comprehensive resource features in-depth discussions of important guidelines and regulations needed to understand and properly meet medical device code-related requirements. Focusing on the practical application of the regulations, the Medical Device Guidelines and Regulations Handbook delivers clear explanations, real-world examples, and annotation on the applicable provisions that will allow you to safely and confidently choose materials and processes for medical device development, testing, and manufacturing.  

  • A critical resource for researchers and professionals in the medical device field;
  • Thoroughly covers ISO 10993, ISO 22442, ISO 14971, ISO 13485, ISO 21534, REACH, RoHS, CLP, EU MDR;
  • Presents simplified guidelines and regulation points.



Prakash Srinivasan Timiri Shanmugam, Ph.D., ERT, is currently working as a senior toxicologist at Avanos Medical, Inc. Before Avanos Medical, he was a subject matter expert in biocompatibility at Baxter International, Inc. and Johnson & Johnson. Dr. Timiri Shanmugam has an MS and a Ph.D. in the specialization of Pharmacology and Toxicology with Chemistry (interdisciplinary) from the University of Madras and completed his postdoctoral research at Tulane University and LSU Health Shreveport, Louisiana. He is the editor of the books Understanding Cancer Therapies (CRC Press), Trends in Development of Medical Devices and Toxicological Aspects of Medical Device Implants (both Academic Press), and the author of several book chapters. He has published research articles in several peer-reviewed international journals and conference proceedings/abstracts.

Thangaraju Pugazhenthan, MBBS, MD, DNB, MNAMS, PGD (Diabetology), is an assistant professor in the Department of Pharmacology at All India Institute of Medical Sciences (AIIMS), Raipur. He previously worked in Central Health Services at the Central Leprosy Teaching and Research Institute. He received an MBBS from Madurai Medical College and did his post-graduate training at the Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh. He has published more than 110 internationally indexed publications, including in The Lancet and The BMJ. He is the author of the books Newer Pharmacological Concepts of Managing Erythema Nodosum Leprosum (Lambert, 2017) and A Pharmacological Guide to Non-Steroidal Anti-Inflammatory Medications (Nova Science Publishers, 2021), and a contributing chapter author for the books Ophthalmology and Otorhinolaryngology in Toxicological Aspects of Medical Device Implants (Elsevier, 2020) and Leprosy: From Diagnosis to Treatment (Nova Science Publishers, 2020).

Nandakumar Palani, M.Sc., is a research and development (R&D) engineer and a subject matter expert with more than 14 years of experience in medical device software engineering and manufacturing. He has a master's degree in electronics from the University of Madras and an advanced diploma in embedded systems. He is the author of several book chapters on software engineering and medical regulations and standards for medical device design and manufacturing.

Thamizharasan Sampath Ph.D., PGDCR, is currently working as a professor in the Department of Pharmacology and as Scientist in Charge, Central Research Lab, at ACS Medical College and Hospital. He received his Master's and Ph.D. degrees in pharmacology from the Post Graduate Institute of Basic Medical Sciences and a post-graduate diploma in clinical research from Annamalai University. Dr. Thamizharasan is the author of Bamboo - The Golden Rice (Lambert, 2018), a book on the use of bamboo in medicine, as well as several book chapters. He has published research articles in peer-reviewed international journals and is a reviewer for medical journals. He is a member of the Institutional Research Ethics Committee, Animal Ethics Committee, and Indian Pharmacological Society.

Erscheint lt. Verlag 22.4.2022
Zusatzinfo VI, 385 p. 14 illus., 12 illus. in color.
Sprache englisch
Themenwelt Medizin / Pharmazie
Schlagworte Biomedical Micro Devices • ISO 13485 • ISO standards • Medical and Health Technologies • Medical Device Design • medical device industry • Medical Device Manufacturing • Medical Devices • medical device standards • Quality management
ISBN-10 3-030-91855-6 / 3030918556
ISBN-13 978-3-030-91855-2 / 9783030918552
Haben Sie eine Frage zum Produkt?
PDFPDF (Wasserzeichen)
Größe: 4,0 MB

DRM: Digitales Wasserzeichen
Dieses eBook enthält ein digitales Wasser­zeichen und ist damit für Sie persona­lisiert. Bei einer missbräuch­lichen Weiter­gabe des eBooks an Dritte ist eine Rück­ver­folgung an die Quelle möglich.

Dateiformat: PDF (Portable Document Format)
Mit einem festen Seiten­layout eignet sich die PDF besonders für Fach­bücher mit Spalten, Tabellen und Abbild­ungen. Eine PDF kann auf fast allen Geräten ange­zeigt werden, ist aber für kleine Displays (Smart­phone, eReader) nur einge­schränkt geeignet.

Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen dafür einen PDF-Viewer - z.B. den Adobe Reader oder Adobe Digital Editions.
eReader: Dieses eBook kann mit (fast) allen eBook-Readern gelesen werden. Mit dem amazon-Kindle ist es aber nicht kompatibel.
Smartphone/Tablet: Egal ob Apple oder Android, dieses eBook können Sie lesen. Sie benötigen dafür einen PDF-Viewer - z.B. die kostenlose Adobe Digital Editions-App.

Buying eBooks from abroad
For tax law reasons we can sell eBooks just within Germany and Switzerland. Regrettably we cannot fulfill eBook-orders from other countries.

Mehr entdecken
aus dem Bereich