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Liste des congrès médicaux, formations santé à Palo Alto : 28 résultats

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Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes

Réf: 28925 Mercredi 20 Février 2019 - Palo Alto US

Editorial This training program will highlight mistakes often made when corrective and preventative actions are not clearly identified and applied during a manufactured product sterility test failure investigation because an ineffective investigational procedure and tool was used to conduct a ...

Conférence & Séminaire: Management

Introduction to Root Cause Investigation for CAPA

Réf: 28930 Jeudi 21 Février 2019 - Palo Alto US

Editorial This CAPA training program will provide an understanding of FDA and ISO requirements, steps in CAPA process and the challenges associated to root cause analysis. Attendees will learn the tools and quality data sources to use during root cause analysis investigation. Objectives If ...

Conférence & Séminaire: Management

HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms

Réf: 29044 Jeudi 21 Février 2019 - Palo Alto US

Editorial Environmental control of pharmaceutical cleanrooms is essential to the manufacture of a quality product. Control of such conditions as airborne particulate, microorganisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the ...

Conférence & Séminaire: Management

Nasal Decolonization as a Tool for Infection Prevention

Réf: 29045 Jeudi 21 Février 2019 - Palo Alto US

Editorial This healthcare compliance webinar will focus on the risk of MRSA colonization to patients and others. Attendees will learn the current practice of nasal screening and isolation for MRSA colonized patients will be described as well as universal decolonization as an alternative will ...

Conférence & Séminaire: Santé Publique, Sécurité sociale, Hôpital

Pharmacokinetics/Biopharmaceutics for Chemists/Analysts

Réf: 29047 Jeudi 21 Février 2019 - Palo Alto US

Editorial This training program will focus on defining and explaining numerous concepts and terminologies in a simple language as related to the safety, efficacy and quality assessment of pharmaceutical products for human use. It will also describe the necessity of understanding the basic ...

Conférence & Séminaire: Management

Current Concepts and Challenges in Cloud Compliance

Réf: 29048 Jeudi 21 Février 2019 - Palo Alto US

Editorial Cloud computing has become perhaps the most critical compliance topic related to computer validation and electronic records. The potential economic and resource advantages to using cloud based environments guarantee that management will expect compliance strategies to be developed ...

Conférence & Séminaire: Informatique

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory

Réf: 29113 Jeudi 21 Février 2019 - Palo Alto US

Editorial This 2-hr laboratory inspection webinar will discuss strategies to implement before your laboratory is about to undergo a pre-approval inspection or a general GMP inspection. It will help you gain an understanding of the key areas that are likely to be the subject of a laboratory ...

Conférence & Séminaire: Management

Bundled Payment Review: How Case Management Can Play a Strategic Role

Réf: 29049 Vendredi 22 Février 2019 - Palo Alto US

Editorial This webinar will teach you how bundled payments actually work as they move from demonstration to reality. It will discuss how case management must become a fully integrated across the continuum model. Objectives By attending this webinar, attendees will be able to become familiar ...

Conférence & Séminaire: Management

Project Management for Computer Systems Validation

Réf: 28931 Mardi 26 Février 2019 - Palo Alto US

Editorial This computer system validation training will highlight the principles of project management that can be applied to 21 CFR Part 11 compliance for Computer Systems Validation and show how you can use project management tenets to deliver on time and on budget, while meeting FDA ...

Conférence & Séminaire: Management

Establishing a Medical Device Security Program

Réf: 28932 Mardi 26 Février 2019 - Palo Alto US

Editorial In this medical devices security webinar you will learn how to establish a Product Security Program that help your organization to put the right people, processes, and technology in one place to solve the changing landscape of connected medical devices and the risks that are ...

Conférence & Séminaire: Hôpital

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

Réf: 29050 Mardi 26 Février 2019 - Palo Alto US

Editorial This training program will discuss the types of human error, the taxonomy of human error, human error reduction initiatives, individual performance, cognitive load and human error, cognitive load categories, and more. Objectives Attention and memory failures are usually associated ...

Conférence & Séminaire: Management

FDA Compliance and Clinical Trial Computer System Validation

Réf: 28936 Mercredi 27 Février 2019 - Palo Alto US

Editorial This webinar will discuss FDA requirements for clinical trial Computer System Validation (CSV) including System Development Life Cycle (SDLC) approach to validation. It will help attendees understand how to leverage the vendor and other external resources to apply the best industry ...

Conférence & Séminaire: Management

Medical Device Employee Training - Requirements and Implementation Tips

Réf: 29051 Mercredi 27 Février 2019 - Palo Alto US

Editorial This webinar will review types of training requirements from the FDA and ISO 13485 for medical device employee. It will discuss techniques for monitoring and documenting training effectiveness. Objectives Understanding FDA and ISO training requirements Understanding how to ...

Conférence & Séminaire: Management

505(b)(2) NDAs

Réf: 29052 Mercredi 27 Février 2019 - Palo Alto US

Editorial In this webinar attendees will learn which products qualify for submissions under section 505(b)(2) of the Federal Food, Drug and Cosmetic Act (FD & C) and the requirements for studies, reference information, and marketing requirements to take advantage of this great sponsorship ...

Conférence & Séminaire: Hôpital, Management

Prevention of Infection in Healthcare Workers

Réf: 28974 Jeudi 28 Février 2019 - Palo Alto US

Editorial For healthcare facilities and long-term care facilities looking to promote employee safety in the workplace, this webinar will provide essential information on structuring your employee health program as per Center of Disease Control (CDC), Occupational Health and Safety ...

Conférence & Séminaire: Hôpital

Prevention of Infection in Healthcare Workers

Réf: 29054 Jeudi 28 Février 2019 - Palo Alto US

Editorial For healthcare facilities and long-term care facilities looking to promote employee safety in the workplace, this webinar will provide essential information on structuring your employee health program as per Center of Disease Control (CDC), Occupational Health and Safety ...

Conférence & Séminaire: Hôpital

FDA Regulations for Environmental Monitoring (EM) Program

Réf: 28975 Lundi 04 Mars 2019 - Palo Alto US

Editorial This training program on applicable regulations pertaining to clean room environmental monitoring (EM) programs will discuss the basics of setting a robust and effective EM program. The course will also detail the relationship between an EM Excursion Program and CAPA and the four ...

Conférence & Séminaire: Hôpital, Gestion & Fiscalité

Batch Record Review and Product Release

Réf: 28977 Mardi 05 Mars 2019 - Palo Alto US

Editorial In this webinar attendees will learn the fundamentals for reviewing batch records in a pharmaceuticals, biologics and medical devices environment. You will hear about the proper training that must be demonstrated before one is considered a suitable reviewer of these critical documents ...

Conférence & Séminaire: Management

How to Write Effective 483 and Warning Letter Responses

Réf: 28978 Mardi 05 Mars 2019 - Palo Alto US

Editorial In this regulatory inspection webinar attendees will learn the importance of developing and submitting a robust, timely response to FDA 483 observations or warning letters; as well as, educate the audience on the essential elements of a thorough response. Also attendees will learn the ...

Conférence & Séminaire: Management

Supplier and Service Provider Controls: FDA Expectations

Réf: 28937 Mercredi 06 Mars 2019 - Palo Alto US

Editorial This training program will provide regulatory requirements (US) of 21 CFR Section 820.50 (purchasing control) for the medical device industry and illustrate the same with examples. It will furnish details on what purchasing/supplier control management systems should ...

Conférence & Séminaire: Management

Failure Modes and Effects Analysis - An effective Risk Management Tool

Réf: 28938 Jeudi 07 Mars 2019 - Palo Alto US

Editorial This Medical device training will acquaint one with the various terms used in risk management and the importance of ISO 14971 & ISO 13485 in the managements of risks during the life cycle of medical devices starting with design and manufacture. Objectives FMEA (Failure Mode ...

Conférence & Séminaire: Management

Engaging Hospitalists in the Case Management Process

Réf: 28979 Jeudi 07 Mars 2019 - Palo Alto US

Editorial In this healthcare compliance webinar attendees will understand the role of the hospitalist, the hospitalist group and the collaboration responsibility with the case management department to ensure compliance with federal regulations, decreasing length of stay, and methods to improve ...

Conférence & Séminaire: Management

The Most Serious FDA 483s - How to Avoid Them

Réf: 28981 Mardi 12 Mars 2019 - Palo Alto US

Editorial This webinar on avoiding serious FDA 483s will explain FDA's changed audit focus based on recent top 483 findings and provide practical tips on how to better prepare your company's internal audit program to avoid serious Form 483 observations.  Objectives Recent FDA audits ...

Conférence & Séminaire: Management

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers

Réf: 28982 Mardi 12 Mars 2019 - Palo Alto US

Editorial This webinar will include a detailed discussion of Contract Manufacturing Organizations (CMO) Quality Agreement topics such as change control, documentation, facilities and equipment, lab controls, sub-contracting, etc. Attendees will learn how to comply with new FDA and EU guidelines ...

Conférence & Séminaire: Management

FDA Regulations for Marketing OTC Drugs in the U.S.

Réf: 28983 Jeudi 14 Mars 2019 - Palo Alto US

Editorial This training program will illustrate why it’s essential to understand FDA regulations and OTC labeling requirements to market OTC drugs in the U.S. Objectives Understanding U.S. FDA regulations and the OTC monograph system and its labeling requirements will help companies assure ...

Conférence & Séminaire: Management

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