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List of dentistry events in Palo Alto : 17 results

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Dentistry meetings - Dentistry educations

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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

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

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

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

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

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

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

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process ...

Ref: 30716 Tuesday November 19th, 2019 - Palo Alto US

Editorial This training program will provide the regulatory requirements (US) for complaint handling in the medical device and pharmaceutical industries. The course will touch on complaint sources, and details will be furnished on the interrelationships regarding complaint handling/change ...

Conference & Seminar: Management

Validation Master Plan - The Unwritten Requirements

Ref: 30385 Wednesday November 20th, 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 ...

Conference & Seminar: Management

Validation Master Plan - The Unwritten Requirements

Ref: 30717 Wednesday November 20th, 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 ...

Conference & Seminar: Management

GxP/GMP Requirements and its Consequences for Documentation and Information Technology Systems

Ref: 30718 Wednesday November 20th, 2019 - Palo Alto US

Editorial Attend this webinar to learn the connection between GxP/GMP with document control and IT systems. Attendees will learn how to manage control documents to pass quality audit and information technology systems in compliance with GxP/GMP ...

Conference & Seminar: Management

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

Ref: 30386 Wednesday December 04th, 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 ...

Conference & Seminar: Management