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Liste des congrès médicaux, formations santé à Palo Alto : 20 résultats

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Technical Writing in the Pharmaceutical Industry

Réf: 30388 Lundi 21 Octobre 2019 - Palo Alto US

Editorial In this webinar, learn how to write technical documents in a highly specialized, highly regulated field like the pharmaceutical industry. It will teach you the techniques that that are easy to understand and help in creating high quality documents with the least amount of ...

Conférence & Séminaire: Pharmacie

Establishing a Robust Supplier Management Program

Réf: 30380 Mardi 22 Octobre 2019 - Palo Alto US

Editorial This course will review regulatory guidance governing Suppliers and the elements of a robust supplier management program including, initial qualification, supplier performance monitoring, and scorecards, supplier audit options, and quality agreement requirements. It will discuss how ...

Conférence & Séminaire: Management

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

Réf: 30266 Mercredi 23 Octobre 2019 - Palo Alto US

Editorial Learn the basic overview of the original medical device Quality Management System -- The US FDA’s CGMP, Quality System Regulation (QSR) under 21 CFR 820. Implementation, training requirements and content, and annual internal audit / inspection expectations. The FDA’s four key areas ...

Conférence & Séminaire: Management, Recherche

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

Réf: 30330 Mercredi 23 Octobre 2019 - Palo Alto US

Editorial Learn the basic overview of the original medical device Quality Management System -- The US FDA’s CGMP, Quality System Regulation (QSR) under 21 CFR 820. Implementation, training requirements and content, and annual internal audit / inspection expectations. The FDA’s four key areas of ...

Conférence & Séminaire: Management

Good Documentation Guideline (Chapter <1029> USP)

Réf: 30382 Jeudi 24 Octobre 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 records.
  Objectives Good Documentation ...

Conférence & Séminaire: Management

Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)

Réf: 30420 Jeudi 24 Octobre 2019 - Palo Alto US

Editorial The objective of this webinar is to compare and contrast between Good Laboratory Practices and Good Manufacturing practices.
  Objectives What are Good Laboratory Practices Why were they created What is the objective of GLPs and how are they associated with GMPs ...

Conférence & Séminaire: Pharmacie

Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2

Réf: 30029 Lundi 04 Novembre 2019 - Palo Alto US

Editorial This webinar will cover the new law on confidentiality of substance use disorder patient records under 42 CFR part 2. This law was previously known as the confidentiality of drug abuse and alcohol abuse records. The new law was effective in 2017. Anyone or any facility that is ...

Conférence & Séminaire: Management, Hôpital, Infirmiers

Practicing Laboratory Safety in the Workplace

Réf: 30421 Mardi 05 Novembre 2019 - Palo Alto US

Editorial In this training program, attendees will gain an understanding of general laboratory safety and common lab operation procedures. The course will also instruct on what PPE to provide such as safety goggles, aprons, gloves, eyewash stations, fire extinguishers, first aid kits, ...

Conférence & Séminaire: Pharmacie

Powerful Closed-loop CAPA - Meeting FDA Expectations

Réf: 30267 Mercredi 06 Novembre 2019 - Palo Alto US

Editorial This 90-minute webinar will show how you can implement a closed-loop CAPA system that meets CGMP requirements and U.S. FDA expectations. You will learn simple, but powerful, tools and methods that you can use regularly and systematically to define and resolve root causes, not just ...

Conférence & Séminaire: Hôpital, Management

Powerful Closed-loop CAPA - Meeting FDA Expectations

Réf: 30334 Mercredi 06 Novembre 2019 - Palo Alto US

Editorial This 90-minute webinar will show how you can implement a closed-loop CAPA system that meets CGMP requirements and U.S. FDA expectations. You will learn simple, but powerful, tools and methods that you can use regularly and systematically to define and resolve root causes, not just ...

Conférence & Séminaire: Management

Basic Clean Room Technology, Operation and Contamination Control in a Nutshell

Réf: 30347 Jeudi 07 Novembre 2019 - Palo Alto US

Editorial Attend this webinar to understand the Clean Room regulations, design, classification, sources and types of particles. Learn how to create a common ground between these varying regulations and requirements. It will discuss the types of micro-organisms, routine monitoring processes, and ...

Conférence & Séminaire: Dentisterie esthétique

Technical Writing: A Detailed Process

Réf: 30419 Mardi 12 Novembre 2019 - Palo Alto US

Editorial Technical Writing: A Detailed Process provides step-by-step instructions for experienced Technical Writers go from the blank screens to the final written presentations. The webinar includes procedures for the creation of document plans and meetings with stakeholders to produce the ...

Conférence & Séminaire: Pharmacie

You have a BI Positive or Product Sterility Positive - Now What?

Réf: 30030 Mardi 19 Novembre 2019 - Palo Alto US

Editorial This webinar will discuss what actions should be taken following a positive result in a sterility test on a biological indicator (BI) during performance qualification or routine testing. It will also explain the various items that should be investigated to determine the root cause ...

Conférence & Séminaire: Recherche

You have a BI Positive or Product Sterility Positive - Now What?

Réf: 30335 Mardi 19 Novembre 2019 - Palo Alto US

Editorial This webinar will discuss what actions should be taken following a positive result in a sterility test on a biological indicator (BI) during performance qualification or routine testing. It will also explain the various items that should be investigated to determine the root cause and ...

Conférence & Séminaire: Hôpital

How to Prepare a Standard Operating Procedure (SOP)?

Réf: 30383 Mardi 19 Novembre 2019 - Palo Alto US

Editorial This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time.
  Objectives Standard Operating Procedures ...

Conférence & Séminaire: Management

Best Practices for an Effective Cleaning Validation Program

Réf: 30384 Mardi 19 Novembre 2019 - Palo Alto US

Editorial This training program will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory ...

Conférence & Séminaire: Hôpital

Validation Master Plan - The Unwritten Requirements

Réf: 30274 Mercredi 20 Novembre 2019 - Palo Alto US

Editorial This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a ...

Conférence & Séminaire: Management

Validation Master Plan - The Unwritten Requirements

Réf: 30385 Mercredi 20 Novembre 2019 - Palo Alto US

Editorial This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's ...

Conférence & Séminaire: Management

4-Hr Virtual Training: How to Respond to an FDA Investigation

Réf: 30386 Mercredi 04 Décembre 2019 - Palo Alto US

Editorial This FDA investigation training program will deconstruct best practices for handling unannounced FDA visits, responding to a 483 or a warning letter, and the effect of an FDA investigation. The program will also discuss basic concepts that should be employed by everyone regulated by ...

Conférence & Séminaire: Management

Contracted Services: Ensuring Compliance with the CMS Hospital CoP Standards, Joint Commission and DNV

Réf: 30031 Lundi 09 Décembre 2019 - Palo Alto US

Editorial This webinar will cover all of the contract requirements for hospitals accredited by the Joint Commission. This standard has been amended every year for the past three years. The CMS telemedicine standard also updated a section in the Joint Commission contract ...

Conférence & Séminaire: Hôpital, Management, Infirmiers