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Congrès médical, Formation Médecine à Palo Alto

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Liste des évènements Médecine à Palo Alto : 31 résultats

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The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process

Réf: 29193 Mercredi 24 Avril 2019 - Palo Alto US

Editorial In this training program, attendees will gain an understanding of how the HCQIA protects your organization and on those who participate in the peer review process in your organization. They will also gain an appreciation of the actions that are required to perfect HCQIA immunity. ...

Conférence & Séminaire: Management

Contemporary Case Management Staffing and Models: Best Practices in the Era of Value-Based Purchasing

Réf: 29195 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This webinar will review contemporary, best practice, case management models including descriptions of the two most commonly used models, the key differences between the models, as well as how they should be designed and structured. The webinar will also discuss the steps needed to re-...

Conférence & Séminaire: Management

CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps

Réf: 29196 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This training program will assist anyone directly or indirectly responsible for the creation, content or validation of CDISC data sets, tables, and data lists used to support research, drug or medical device efficacy and safety in a regulatory submission. Professionals in the ...

Conférence & Séminaire: Hôpital, Management

The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process

Réf: 29363 Mercredi 24 Avril 2019 - Palo Alto US

Editorial In this training program, attendees will gain an understanding of how the HCQIA protects your organization and on those who participate in the peer review process in your organization. They will also gain an appreciation of the actions that are required to perfect HCQIA immunity. ...

Conférence & Séminaire: Hôpital, Management, Sages-femmes, Infirmiers

Contemporary Case Management Staffing and Models: Best Practices in the Era of Value-Based Purchasing

Réf: 29364 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This webinar will review contemporary, best practice, case management models including descriptions of the two most commonly used models, the key differences between the models, as well as how they should be designed and structured. The webinar will also discuss the steps needed to ...

Conférence & Séminaire: Hôpital, Management, Infirmiers

CDISC Mapping 3: Compare and Contrast SDTM and ADaM Steps

Réf: 29376 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This training program will assist anyone directly or indirectly responsible for the creation, content or validation of CDISC data sets, tables, and data lists used to support research, drug or medical device efficacy and safety in a regulatory submission. Professionals in the ...

Conférence & Séminaire: Management

Implementing a Quality Management System

Réf: 29377 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This GLP quality system webinar provides a general overview of the Proposed Rule, a GLP QMS and its implementation, GAP analysis, Plan-Do-Check-Act cycle, process control and optimization theory and quality audits are utilized for the analysis of an existing QMS and the potential ...

Conférence & Séminaire: Management

Implementing a Quality Management System

Réf: 29518 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This GLP quality system webinar provides a general overview of the Proposed Rule, a GLP QMS and its implementation, GAP analysis, Plan-Do-Check-Act cycle, process control and optimization theory and quality audits are utilized for the analysis of an existing QMS and the potential ...

Conférence & Séminaire: Management

Creating a Risk-based Supplier Management program

Réf: 29519 Mercredi 24 Avril 2019 - Palo Alto US

Editorial This webinar on supplier controls will provide you the information you need to assure your supplier management program is in compliance with the latest FDA, European and international guidelines requiring a risk-based supplier management program. We will look at how to improve your ...

Conférence & Séminaire: Management

Human Error Investigations, Root Cause Determination and CAPA Effectiveness

Réf: 29194 Jeudi 25 Avril 2019 - Palo Alto US

Editorial This training program will offer attendees an understanding of human error, its factors and causes. The program will also identify the regulatory and business importance of human error prevention and define the process to manage human error deviations. Objectives Understand ...

Conférence & Séminaire: Management

How to Manage Your Vendors in Clinical Research

Réf: 29373 Jeudi 25 Avril 2019 - Palo Alto US

Editorial This vendor management webinar will show you how to choose the right vendor, onboarding and set up, manage vendor performance, manage issues and ensure compliance with current FDA regulations and ICH guidelines and have a smooth-running clinical study. Objectives Sponsors are ...

Conférence & Séminaire: Management, Gestion & Fiscalité

Human Error Investigations, Root Cause Determination and CAPA Effectiveness

Réf: 29374 Jeudi 25 Avril 2019 - Palo Alto US

Editorial This training program will offer attendees an understanding of human error, its factors and causes. The program will also identify the regulatory and business importance of human error prevention and define the process to manage human error deviations. Objectives Understand ...

Conférence & Séminaire: Hôpital, Management, Gestion & Fiscalité

Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities

Réf: 29375 Jeudi 25 Avril 2019 - Palo Alto US

Editorial This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel. Besides the US, the use of DMFs in the EU, Canada and Australia will also be discussed. ...

Conférence & Séminaire: Pharmacie, Management

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results

Réf: 29520 Jeudi 25 Avril 2019 - Palo Alto US

Editorial This training on pharmaceutical laboratory OOS investigations will explain how to recognize and address atypical or out of specification results, using approaches which have been recommended by regulatory authorities, performing appropriate ...

Conférence & Séminaire: Management

The Brazilian Reimbursement System

Réf: 29521 Jeudi 25 Avril 2019 - Palo Alto US

Editorial In this webinar attendees will learn the legal and regulatory framework for reimbursement system in Brazil to have better and effective result when marketing with medical and drug product in Brazil.   Objectives How does the Reimbursement System ...

Conférence & Séminaire: Management

Good Documentation Guideline (Chapter <1029> USP)

Réf: 29522 Vendredi 26 Avril 2019 - Palo Alto US

Editorial This webinar will familiarize participants with USP Chapter <1029> on good documentation guidelines. This session will wrap up the general concept and will provide information as to what needs to be documented in certain ...

Conférence & Séminaire: Management, Recherche

Compliance Measures for Case Managers

Réf: 29372 Jeudi 02 Mai 2019 - Palo Alto US

Editorial   This program will review the compliance issues that most greatly impact your practice such as the 2-midnight rule, the NOTICE Act, HINNs, the important message from Medicare and others. The Joint Commission is now monitoring these issues when they have deemed status from ...

Conférence & Séminaire: Management, Hôpital

Handling OOS Test Results and Completing Robust Investigations

Réf: 29536 Jeudi 02 Mai 2019 - Palo Alto US

Editorial This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which ...

Conférence & Séminaire: Hôpital, Management

Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Réf: 29537 Jeudi 02 Mai 2019 - Palo Alto US

Editorial This webinar will help you better understand test method validations to verify the performance of a Medical Device, global reference standards, the FDA requirements and how to perform successful TMV to ensure your inspection of verification is effective, using detailed real-life case ...

Conférence & Séminaire: Recherche

Stability Studies and Estimating Shelf Life

Réf: 29538 Lundi 06 Mai 2019 - Palo Alto US

Editorial In this webinar attendees will learn the useful methods and techniques for conducting a stability study and analyzing the resulting data for estimating shelf life. This webinar will provide the answers to help participants immediately apply the presented methods. The interpretation ...

Conférence & Séminaire: Recherche, Management

Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU's MDD Requirements

Réf: 29562 Mardi 07 Mai 2019 - Palo Alto US

Editorial This 90-minute webinar will examine in detail the U.S. FDA and EU MDD requirements for DHFs, DMRs, DHRs, and TF/DDs - their formats, content, and their commonalities, differences, interrelationships, and similarities.   Objectives Global companies must ...

Conférence & Séminaire: Management

Effective Records Management and Document Control for Medical Devices

Réf: 29563 Mardi 07 Mai 2019 - Palo Alto US

Editorial In this webinar attendees will learn the QSR and ISO 13485 requirements for document control and the ideas associated with the development and control of quality documentation. Also attendees will get knowledge on methods and practices that will improve the clarity and control of ...

Conférence & Séminaire: Hôpital, Management

Production and Process Controls - Ensuring your medical device conforms to its specifications

Réf: 29564 Mercredi 08 Mai 2019 - Palo Alto US

Editorial This presentation will cover the FDA regulations (21 CFR Subpart G Section 820.70) regarding production and process controls and how each requirement listed within the regulation can be addressed. We’ll go over examples of documentation you can use to fulfill the requirements of this ...

Conférence & Séminaire: Management

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

Réf: 29565 Jeudi 09 Mai 2019 - Palo Alto US

Editorial Learn how to use Microsoft Excel spreadsheets for GXP data to ensure compliance with 21 CFR Part 11 and reduce validation cost and time. Objectives This course will train attendees on best practices to create a spreadsheet that is GxP compliant using Microsoft Excel. Attendees ...

Conférence & Séminaire: Biologie, Management

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Réf: 29566 Mardi 14 Mai 2019 - Palo Alto US

Editorial This webinar will discuss various US and international regulatory requirements, testing requirements for environmental monitoring program, current air and surface monitoring for measurement of no-viable particulate, microbial contamination, contamination due to personnel (gowning ...

Conférence & Séminaire: Management

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