• Regeln für den Audio-Bereich:

    Allgemeine Boardregeln: MyBoerse-bz-Regelwerk Regelwerk Audioboerse

    1. Das richtige Forum

    Wähle ein passendes Unterforum für dein Angebot

    2. Doppelte Threads vermeiden / Ein Thread pro Interpret


    Da es hier langsam ausartet mit gleichen Interpreten, aber verschiedenen Jahren, gilt ab sofort: Nur noch ein Thread pro Interpret, unabhängig von der Jahreszahl der verschiedenen Alben. Wünschenswert wäre es wenn ihr den Titel ab sofort so benennt: Interpret - Diskographie

    Um Doppelpost zu vermeiden, nutze vor dem Posten die Suchenfunktion. Gibt es schon einen passenden Thread, dann poste Dein Angebot dort hinein. Für einzelne Alben einer Sammlung bzw. Hörbuchreihen bitte in den passenden Sammelthreads posten.

    3. Der richtige Titel

    Gib dem Thread einen einfachen aber vernünftigen Titel, der zum Angebot passt. Um den Thread besser über die Suche zu finden, solltest du einen normalen Titel benutzen. Bei Threads in den Foren Musik, HQ Audio / Lossless und Soundtracks / OST immer das Jahr am Ende des Threadtitels in Klammern angeben, z.B.: Interpretname - Albumname (2016)

    4. Die richtigen Angaben

    Ein Thread/Thema in der Audio-Börse muss dem User Informationen über das Angebot geben können.

    Pflichtangaben:

    Bild des Uploads
    Genre
    Bitrate der Musik Datei: in Kbit/s
    Hoster
    Größe in MB oder GB
    Tracklist

    Optional: Angabe wenn Cover dabei sind.


    Sollte ein Angebot diese Pflichtangaben nicht beinhalten, wird der Verfasser darauf hingewiesen. Sollte dieses dann nicht geändert werden, werden die Beiträge gelöscht.

    (Sollte der Upload nicht als mp3 vorliegen, sondern als ogg/Bin/Cue o.Ä., dann ist dies auch eine Pflichtangabe)

    5. Defekte/nicht verfügbare Links und andere Probleme mit einem Upload

    Sollte ein Upload down sein, dann meldet es per PN dem Uploader. Gibt es zwei Threads zum gleichen Thema oder ein Upload im falschen Forum, dann meldet dies via "Beitrag melden" Funktion, diese befindet sich neben dem Bedanken-Button.

    6. Reupp- /Hosteranfragen
    Reuppanfragen oder auch Anfragen ob es bei einem anderen Hoster geuppt werden kann, bitte direkt per PN an den Uploader und nicht in den Thread.
  • Bitte registriere dich zunächst um Beiträge zu verfassen und externe Links aufzurufen.

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Certificate Course- Clinical Evaluation Report (Cer) Writing

Tutorials

MyBoerse.bz Pro Member
eb38f68f68e1a269ed7757ca5396cfa2.jpeg

Free Download Certificate Course- Clinical Evaluation Report (Cer) Writing
Published 11/2023
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 581.67 MB | Duration: 1h 17m
Learn the art of Clinical Evaluation Report (CER) writing

What you'll learn
Understand the Clinical Evaluation Report (CER) Writing Process: Learn the essential components and steps involved
Comprehend Regulatory Requirements: Gain insights into the regulatory landscape governing CERs
Conduct Device Evaluation and Clinical Data Analysis: Acquire the skills to evaluate medical devices and analyze clinical data to support CER development
Create Compliant and Comprehensive CERs: Master the art of authoring comprehensive, compliant, and evidence-based CERs tailored to specific device types.
Requirements
No specific prerequisites are required to enroll in this course. However, a background in medicine, pharmacy, science, or a related discipline is beneficial. This course is suitable for: Professionals with a minimum of 4 years of post-secondary education in medicine, pharmacy, science, or allied disciplines. Recent graduates interested in pursuing a career in clinical research for medical devices. Experienced professionals seeking to enhance their expertise in clinical evaluation report (CER) writing for medical devices. Individuals from diverse educational backgrounds who wish to explore the field of medical device research and understand the supplementary education needed to excel in this industry.
Description
Unlock the key to creating precise and compliant Clinical Evaluation Reports (CERs) with our comprehensive Udemy course. Designed for professionals in the medical device industry, quality managers, regulatory affairs experts, and aspiring clinical evaluators, this course offers a step-by-step guide to mastering the art of Clinical Evaluation Report Writing.What You'll Learn:Fundamentals of Clinical Evaluation: Gain a solid understanding of clinical evaluation principles, regulations, and the role of clinical reports in the medical device industry.CER Structure and Components: Learn to structure your reports effectively, including device description, context of evaluation, benefit claims, risk assessment, and more.Data Collection and Assessment: Master the process of data collection, evaluation, and conclusion drawing, with in-depth insights into source evaluation and documentation.Scientific Writing: Enhance your scientific writing skills with tips for maintaining clarity and objectivity in your reports, citing sources correctly, and using the appropriate writing style.Interplay with Regulatory Requirements: Explore the connections between clinical evaluation, risk management, clinical investigation, post-market surveillance, and post-market clinical follow-up, ensuring compliance with MDR and other regulations.Join us on a journey to unlock the secrets of Clinical Evaluation Report Writing and elevate your career in the medical device field. Enroll now to embark on a path toward mastery.
Overview
Section 1: Section 1: Introduction
Lecture 1 Introduction
Section 2: Section 2: Overview of Clinical Data Collection and Evaluation
Lecture 2 Overview of Clinical Data Collection and Evaluation
Section 3: Section 3: Overview of the European regulations
Lecture 3 Overview of the European regulations
Section 4: Section 4: additional MDR requirements compared to the MDD
Lecture 4 Additional MDR requirements compared to the MDD
Section 5: Section 5: MEDDEV 2.7/1
Lecture 5 MEDDEV 2.7/1
Section 6: Section 6: Exemptions from Clinical Evaluation
Lecture 6 Exemptions from Clinical Evaluation
Section 7: Section 7: Documenting Clinical Evaluation
Lecture 7 Documenting Clinical Evaluation
Section 8: Section 8: CER content and literature search
Lecture 8 CER content and literature search
Section 9: Section 9: CER Report and Drawing Conclusions
Lecture 9 CER Report and Drawing Conclusions
Section 10: Quiz
This course is ideal for recent graduates as well as experienced professionals in the fields of science, medicine, and allied disciplines who are interested in building a career in clinical research, particularly in clinical evaluation report (CER) writing for medical devices. It is also suitable for graduates from other areas looking to understand the educational requirements necessary to enter the dynamic world of clinical research and development within the medical device industry. Whether you are starting your career or seeking to enhance your skills, this course provides valuable knowledge and insights into the critical field of CER writing for medical devices.

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