Clinical evaluation report training

Elsmar Forum Sponsor
#3
The European Medical Writers Association (EMWA) has a conference twice yearly, with very good workshops. They have workshops on CER writing and literature search, among other. LS academy is another training provider with very good courses on medical devices. Some of their course leaders are also teaching at the EMWA workshops. LS academy is much more expensive compared to EMWA but provides courses more frequently.
I hope that helps!
 
Thread starter Similar threads Forum Replies Date
shimonv Clinical evaluation report for class I device EU Medical Device Regulations 18
S Regular updates of clinical evaluation report EU Medical Device Regulations 6
S Australia TGA Clinical Evaluation Report (CER) Other Medical Device Regulations World-Wide 0
dgrainger Informational MDCG 2020:13 - Clinical evaluation assessment report template EU Medical Device Regulations 0
D Clinical Evaluation Report - Consultant Recommendations Consultants and Consulting 9
A Medical device CER (clinical evaluation report) training/seminar services EU Medical Device Regulations 2
H Addressing of Undesirable side-effects, harms, risks and side-effects in clinical evaluation report (CER) EU Medical Device Regulations 12
S Medical device CER (clinical evaluation report) according to MDR EU Medical Device Regulations 24
M SOPs, Plans and Report templates for Clinical Evaluation of EU MDR Other Medical Device Related Standards 11
TheMightyWife Copyright for articles used in CER (Clinical Evaluation Report) EU Medical Device Regulations 16
Q Evidence of precautions (clinical evaluation report, risk management report) EU Medical Device Regulations 6
C Qualification of Evaluator - Clinical Evaluation Report MEDDEV 2.7.1 Rev 04 CE Marking (Conformité Européene) / CB Scheme 3
Q Sample of the MEDDEV 2.7.1 rev 4 Clinical Evaluation Report wanted Document Control Systems, Procedures, Forms and Templates 18
L Clinical Evaluation Report Updating Procedure Other Medical Device Related Standards 5
R Qualification of Evaluator - Clinical Evaluation Report MEDDEV 2.7.1 Rev 04 Other Medical Device and Orthopedic Related Topics 1
E CER (Clinical Evaluation Report) MEDDEV Version 4 Template wanted CE Marking (Conformité Européene) / CB Scheme 5
Gamula CFDA Clinical Evaluation Report (China) China Medical Device Regulations 4
M Clinical Evidence - Clinical Evaluation Report for Class I medical devices EU Medical Device Regulations 1
E Biocompatability Clinical Evaluation Report ISO 13485:2016 - Medical Device Quality Management Systems 4
E Medical Device Class 2a CE Mark Clinical Evaluation Report CE Marking (Conformité Européene) / CB Scheme 3
E Clinical Evaluation Report for a Delivery System ISO 13485:2016 - Medical Device Quality Management Systems 2
K Clinical Evaluation Report Article Summary Requirements EU Medical Device Regulations 5
A Clinical Evaluation Report Examples and Finding Articles for support EU Medical Device Regulations 4
I Clinical evaluation for legacy device EU Medical Device Regulations 16
K Continue to do clinical evaluation? or transfer to RA? or focus on clinical studies as MA? Career and Occupation Discussions 1
O CLINICAL EVALUATION - VACCUM PLANTS Other Medical Device Related Standards 4
E DESIGN VALIDATION, USABILITY AND CLINICAL EVALUATION request Medical Device and FDA Regulations and Standards News 0
S Clinical Evaluation of equivalent device EU Medical Device Regulations 6
L Clinical evaluation plan EU Medical Device Regulations 17
M Procedure for clinical evaluation according to new MDR EU Medical Device Regulations 11
P GSPRs / Clinical Evaluation EU Medical Device Regulations 3
silentmonkey Overall Benefit/Risk Analysis - Risk Management VS Clinical Evaluation ISO 14971 - Medical Device Risk Management 3
Q Summative Usability Evaluation Testing: prior or during Clinical Investigation? Human Factors and Ergonomics in Engineering 10
M Clinical Evaluation Benchmark vs. Equivalent EU Medical Device Regulations 2
B Clinical Evaluation Expert Panels - MDR EU Medical Device Regulations 1
T Clinical evaluation of a new medical device EU Medical Device Regulations 0
S A clinical performance evaluation study with an IVD product as Investagional Use product - Clinical Monitor requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
R Clinical evaluation without clinical data - MDR Article 61(10) EU Medical Device Regulations 9
M Clinical Evaluation Plan vs. PMCF Plan EU Medical Device Regulations 33
M Can someone share a scrubbed version of Clinical Evaluation Plan (CEP) EU Medical Device Regulations 8
S EU MDR Annex XIV - Clinical Evaluation Plan - What do these methods mean? EU Medical Device Regulations 16
S Clinical Evaluation - Is this an ISO 13485:2016 requirement? ISO 13485:2016 - Medical Device Quality Management Systems 4
M Informational How to perform a clinical evaluation of medical devices – Part 2 – Level of clinical evidence and what sufficient clinical evidence means Medical Device and FDA Regulations and Standards News 9
M Informational How to perform a clinical evaluation of medical devices – Part 1 – Overview and sample of activities Medical Device and FDA Regulations and Standards News 0
T EU MDR Article 61- Clinical Evaluation EU Medical Device Regulations 2
pashah Looking for Clinical Evaluation SOP acc. MEDDEV and EU MDR Other Medical Device Related Standards 1
M CER (Clinical Evaluation Reports) updates - Product Codes EU Medical Device Regulations 2
M Informational IMDRF – Proposed update to Clinical Evaluation documents Medical Device and FDA Regulations and Standards News 0
M Informational MDCG 2019-3 Interpretation of Article 54(2)b – Pre- market clinical evaluation consultation procedure with the involvement of expert panels Medical Device and FDA Regulations and Standards News 0
TheMightyWife Clinical Evaluation MEDDEV 2.7.1 Rev 4 demonstration of equivalence EU Medical Device Regulations 6

Similar threads

Top Bottom