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List of medical conferences and educations - cme in Palo Alto : 40 results

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Technical Writing in the Pharmaceutical Industry

Ref: 30388 Monday October 21st, 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 ...

Conference & Seminar: Pharmacy

Establishing a Robust Supplier Management Program

Ref: 30380 Tuesday October 22nd, 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 ...

Conference & Seminar: Management

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

Ref: 30266 Wednesday October 23rd, 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 ...

Conference & Seminar: Management, Research

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

Ref: 30330 Wednesday October 23rd, 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 ...

Conference & Seminar: Management

Good Documentation Guideline (Chapter <1029> USP)

Ref: 30382 Thursday October 24th, 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 ...

Conference & Seminar: Management

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

Ref: 30420 Thursday October 24th, 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 ...

Conference & Seminar: Pharmacy

The Mindset of an FDA Employee

Ref: 30700 Friday November 01st, 2019 - Palo Alto US

Editorial Productive interactions with FDA personnel are key to a successful company. By unstinting the mindset of FDA employees, you greatly increase the likelihood of productive interactions that will aid you company in the key area of FDA regulation. For most firms the most common ...

Conference & Seminar: Hospital

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

Ref: 30029 Monday November 04th, 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 ...

Conference & Seminar: Management, Hospital, Nurses

Practicing Laboratory Safety in the Workplace

Ref: 30421 Tuesday November 05th, 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, ...

Conference & Seminar: Pharmacy

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Ref: 30703 Tuesday November 05th, 2019 - Palo Alto US

Editorial This 21 CFR Part 11 compliance training will guide you through the requirements of Part 11 and will also explain its 3 primary areas: SOPs, product features and validation (10 step risk based approach).
  Objectives This webinar describes exactly what is required for ...

Conference & Seminar: Management

Powerful Closed-loop CAPA - Meeting FDA Expectations

Ref: 30267 Wednesday November 06th, 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 ...

Conference & Seminar: Hospital, Management

Powerful Closed-loop CAPA - Meeting FDA Expectations

Ref: 30334 Wednesday November 06th, 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 ...

Conference & Seminar: Management

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

Ref: 30347 Thursday November 07th, 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 ...

Conference & Seminar: Cosmetic dentistry

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

Ref: 30707 Thursday November 07th, 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 ...

Conference & Seminar: Management

Aseptic Processing Overview and Validation

Ref: 30708 Monday November 11th, 2019 - Palo Alto US

Editorial This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable personnel behaviors. Objectives At the completion of this course, attendees will be able to: Explain the ...

Conference & Seminar: Management

Technical Writing: A Detailed Process

Ref: 30419 Tuesday November 12th, 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 ...

Conference & Seminar: Pharmacy

How to Conduct Annual Product Reviews to Achieve GMP Compliance Annual

Ref: 30709 Tuesday November 12th, 2019 - Palo Alto US

Editorial This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe.
  Objectives This webinar will ...

Conference & Seminar: Management

Writing and Revising SOPs for Increased Operational Efficiency

Ref: 30711 Tuesday November 12th, 2019 - Palo Alto US

Editorial This webinar will discuss how to more effectively write and revise standard operating procedures (SOPs) with a focus on increasing operational efficiencies.
  Objectives What is an SOP? Ways to structure systems of SOPs Examples of sections to include in an ...

Conference & Seminar: Management

Conducting Successful FDA Meetings

Ref: 30712 Friday November 15th, 2019 - Palo Alto US

Editorial If you develop or manufacture a product regulated by FDA you will need to interact with FDA employees. Knowing what makes FDA employees the way they are, will help immensely in understanding how to deal with FDA.
  Objectives Become familiar the types of jobs within FDA ...

Conference & Seminar: Management

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

Ref: 30030 Tuesday November 19th, 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 ...

Conference & Seminar: Research

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

Ref: 30335 Tuesday November 19th, 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 ...

Conference & Seminar: Hospital

How to Prepare a Standard Operating Procedure (SOP)?

Ref: 30383 Tuesday November 19th, 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 ...

Conference & Seminar: Management

Best Practices for an Effective Cleaning Validation Program

Ref: 30384 Tuesday November 19th, 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 ...

Conference & Seminar: Hospital

How to Prepare a Standard Operating Procedure (SOP)?

Ref: 30713 Tuesday November 19th, 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 Record compliance with examples What ...

Conference & Seminar: Management

Best Practices for an Effective Cleaning Validation Program

Ref: 30715 Tuesday November 19th, 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 ...

Conference & Seminar: Management

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