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1478 Search result(s):
Author Seminar Clinical Evaluation  
This practical seminar helps you, as an author, plan your clinical evaluation optimally, carry it out efficiently, and document it compliantly.  
Beginners' Seminar Clinical Evaluation  
We introduce you to the clinical evaluation process and show you how to review and assess clinical evaluation files in a targeted manner.  
Seminar MDR in Detail  
You will gain an overview of the most important regulatory requirements, relevant standards, guidelines, and best practices in Europe.  
Compact Seminar Medical Device Regulation (MDR)  
You get a compact overview of the most important requirements of the MDR and learn how to implement them efficiently and within the applicable transition periods.  
Seminar Post-Market Surveillance under MDR  
Learn about the regulatory requirements for post-market surveillance (PMS) and how to implement them in your company without unnecessary effort.  
Blended Learning  Literature Research for Medical Writers  
Learn how to conduct targeted and successful literature research as part of your clinical evaluation and document it in accordance with MDR.  
Basic Seminar Quality Management according to ISO 13485  
In this seminar, you will learn what ISO 13485:2021 requires and how your company can confidently pass audits while reducing QM bureaucracy.  
Seminar Medical Device Single Audit Program (MDSAP)  
This seminar helps you understand the principles and requirements of the MDSAP and derive the necessary preparatory measures.  
Course Certified ISO 13485 Lead Auditor  
The five-day course helps you understand the requirements of ISO 13485 and apply them successfully as a lead auditor.  
Seminar Purchasing and Supplier Management  
Learn to understand the requirements of MDR/IVDR and ISO 13485 for purchasing and supplier management in detail and apply them accordingly in your company.  
Results 281 until 290 out of 1478
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