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Validation: : Prochains Evénements, congres, formations, conférences medicales

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RESULTAT DE LA RECHERCHE : 10
: Validation:
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Colloque Informatique médical : Medical Device Software: An Incremental Approach to Risk and Quality Management
Course "Medical Device Software: An Incremental Approach to Risk and Quality Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recert...
Secteurs concernés: Informatique médical -
Conférences en ligne Soins Infirmiers : Computer System Validation 2018 Fundamentals
Overview: FDA requires that all software in computer systems used in GxP activities must be validated. Validation of computer system software is completely different than validation of device softwar...
Secteurs concernés: Biomedical -Soins Infirmiers -
Congrès Biomedical : Applied Statistics for Scientists and Engineers seminar at Boston
Description: Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting valid...
Secteurs concernés: Biomedical -Equipement médical -
Conférence / Séminaire Biomedical : Validation Sampling Plans for Process Validation [Latest]
Overview: Select from among these sampling plans that plan which offers the best balance between the number of units tested and the risk of failing the validation How to identify when sampling plans...
Secteurs concernés: Biomedical -Biotechnologie -
Tags: Education
Conférence / Séminaire Biotechnologie : Record Keeping Best Practices [FDA and EMA] Documentation
Overview: Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for a successful project completion in...
Secteurs concernés: Biotechnologie -Santé publique -
Conférence / Séminaire Biomedical : Business Continuity Planning for [Computer Systems] Operations
Overview: Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacture, testing, distribution and management of a product in the pharm...
Secteurs concernés: Biomedical -Biotechnologie -
Conférence / Séminaire Biotechnologie : Quality by Design - Essential Techniques for Medical Devices
Description: Design Controls are essential for producing safe and effective medical devices. And Design Controls are considered a critical process by the FDA. Yet, Design Controls are still one of th...
Secteurs concernés: Biotechnologie -Equipement médical -
Colloque Biotechnologie : Excel Spreadsheet Validation 2018 Tools and Techniques
Description: Spreadsheets such as Excel, are available for creating a wide range of end user applications, including widespread use in the laboratory, creating customized statistical analyses, the cr...
Secteurs concernés: Biotechnologie -Informatique médical -
Conférence / Séminaire Biotechnologie : Data Integrity in Clinical Trials in [Latest methods]
Overview: The clinical data recording process, however, as inspected/audited by inspectors/auditors is initiated with the recorded data, either in the Case Report Form, or in some other system, or in...
Secteurs concernés: Biomedical -Biotechnologie -Santé publique -
Colloque Biotechnologie : Compliant with 21 CFR Part 11, data integrity, SaaS/Cloud, and EU GDPR
Description: • This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintain...
Secteurs concernés: Biotechnologie -Santé publique -
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