clinical study training
Performance Evaluation and Clinical Evidence for IVDs Training Course
If you are involved in planning, conducting or documenting performance evaluation and clinical performance studies for IVD devices in Europe, this intensive one day course will enable a greater understanding of performance evaluation for In Vitro Diagnostic devices under the IVD Regulation, how performance ...
By British Standards Institution (BSI) based in Herndon, VIRGINIA (USA). from Medical Device Regulatory Training - Specialist Training Training line
ASA - Research Training
ASA’s training offer analyses, interprets and recounts the development of laser therapy and magneto therapy with very practical methods, based on the supervision and collaboration with a team of educators – doctors and researchers – with a recognised scientific ...
By ASAlaser based in Arcugnano (VI), ITALY.
Berlin Heart - Individual Education and Training Program
The Berlin Heart Academy offers an individual education and training program. Staff members of the Clinical Affairs department carry this training out. Due to the long clinical experience of our trainers the program is practice-oriented and tailored to your needs. The training is complemented by case ...
By Berlin Heart GmbH based in Berlin, GERMANY.
Clinical Trials Monitoring - Comprehensive Training Package (4 Courses)
This comprehensive training package of four courses covers clinical trial monitoring techniques, audit procedures and the setting-up of Data Monitoring Committees ...
By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Clinical Research Training line
Skin and Soft Tissue Infections (SSTI) Cause
Staphylococcus aureus (S. aureus) is the leading cause of skin and soft tissue infections (SSTI), also referred to as skin and skin structure infections. Methicillin-resistant S. aureus (MRSA) is a predominant cause of hospital- and community-acquired SSTI. Recent studies conducted by the US Department of ...
By NovaDigm Therapeutics, Inc. based in Grand Forks, NORTH DAKOTA (USA).
21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials
Conducting clinical trials in a rapidly evolving electronic environment presents a unique challenge to the medical device industry where not only quality (GLP/GMP) plays an essential role – but collecting accurate, maintaining viable data (GCP) as part of continuous process improvement (while mitigating ...
By ComplianceOnline based in Palo Alto, CALIFORNIA (USA). from Clinical Regulatory Compliance Training Training line
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