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List of medical conferences and seminars in Palo Alto : 37 results

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Health conference and seminar in Palo Alto

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Technical Writing in an Industrial Environment

Ref: 30365 Thursday September 19th, 2019 - Palo Alto US

Editorial Attend this webinar to learn the logical, fast and simple process of how to easily write any document that your company requires. Explore how to organize collected information, write the document and address the comments from reviewers and approvers.
  Objectives Technical ...

Conference & Seminar: Management

Good Documentation Practice and Record Keeping Regulations (FDA & EMA)

Ref: 30377 Thursday September 19th, 2019 - Palo Alto US

Editorial   In this webinar, we will discuss the definition, purpose, importance of GDP, General rules of GDP, GDP as it applies to laboratory notebook documentation, US Pharmacopeia General Chapter <1029>, and introduction “Good Documentation Guidelines”. We will also briefly ...

Conference & Seminar: Management

How to Develop, Implement and Manage an Effective Change Control Program

Ref: 30378 Thursday September 19th, 2019 - Palo Alto US

Editorial This Change Control training program will discuss regulatory expectations from the FDA, EU and ICH perspective, review all the required components of a thorough Change Control program; as well as, discuss the elements regarding successful management an effective Change Control ...

Conference & Seminar: Management

Post Market Surveillance with the new Medical Device Regulation EU MDR 745/2017

Ref: 30327 Friday September 20th, 2019 - Palo Alto US

Editorial
This webinar will help you understand the requirements of the new medical device regulation EU MDR 745/2017 and teach you how to create the reports. The understanding of the changes and how to implement last-minute changes until May 2020 is essential to keep your certificates and ...

Conference & Seminar: Hospital

FDA's Ambitious Regulation of Social Media

Ref: 30264 Tuesday September 24th, 2019 - Palo Alto US

Editorial FDA regulates advertising and promotion material as labeling. The legal definition of labeling covers just about anything that explicitly or implicitly conveys a message intended to affect a person’s behavior and decision outcomes. How FDA applies its legal tenants of false and ...

Conference & Seminar: Management & Taxation

FDA's Ambitious Regulation of Social Media

Ref: 30275 Tuesday September 24th, 2019 - Palo Alto US

Editorial FDA regulates advertising and promotion material as labeling. The legal definition of labeling covers just about anything that explicitly or implicitly conveys a message intended to affect a person’s behavior and decision outcomes. How FDA applies its legal tenants of false and ...

Conference & Seminar: Management, Diet & Nutrition

The Regulation of in-house IVDs and accreditation of laboratory users in Australia

Ref: 30337 Wednesday September 25th, 2019 - Palo Alto US

Editorial Attend this webinar to understand the definitions of in-house IVDs, the regulatory requirements including classification & essential principles, the NATA requirements related to how and when IVDs can be used as a research or diagnostic tool and the current laboratory supervision ...

Conference & Seminar: Hospital

Regulatory Inspections - How to prepare for a visit from an FDA Auditor

Ref: 30379 Wednesday September 25th, 2019 - Palo Alto US

Editorial This FDA audit webinar will highlight the purpose of FDA audits and scope, Understanding of QSIT audit and how to develop an audit preparedness plan. It will also give understanding of what the FDA will look for at the conclusion of your audit and how to communicate with FDA before ...

Conference & Seminar: Management

Understanding FDAs Governance of Prescription Drug Development: Manufacturing/cGMPs, Submission Process and Post Approval Commitments - ...

Ref: 30406 Wednesday September 25th, 2019 - Palo Alto US

Editorial In this webinar, we will review in detail major considerations to be well-thought-out during the prescription drug product development process. We will review in depth FDA cGMPs and their importance in drug manufacturing. We will review the submission process and post-approval ...

Conference & Seminar: Management

EU ISO 13485:2016 Medical Device Quality Management System

Ref: 30265 Wednesday October 02nd, 2019 - Palo Alto US

Editorial Learn the basic overview of the international medical device Quality Management System -- EU’s Quality Management System under ISO 13485:2016. Implementation, training requirements, content and annual internal audit / inspection ...

Conference & Seminar: Management

EU ISO 13485:2016 Medical Device Quality Management System

Ref: 30328 Wednesday October 02nd, 2019 - Palo Alto US

Editorial Learn the basic overview of the international medical device Quality Management System -- EU’s Quality Management System under ISO 13485:2016. Implementation, training requirements, content and annual internal audit / inspection expectations.
  Objectives In the U. S., the ...

Conference & Seminar: Management

Reducing memory and attention failures/errors: Understanding Cognitive Load

Ref: 30413 Wednesday October 02nd, 2019 - Palo Alto US

Editorial Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human errors start at the design stage and usually factors associated ...

Conference & Seminar: Pharmacy

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, ...

Ref: 30326 Tuesday October 08th, 2019 - Palo Alto US

Editorial This webinar will focus on the key regulatory requirements for medical devices for the participating MDSAP countries of U.S., Canada, Brazil, Australia and Japan. It will address key topics such as device classification, licensing pathways, medical device GMP, inspections, device ...

Conference & Seminar: Management

Root Cause Analysis - The Heart of Corrective Action

Ref: 30329 Tuesday October 08th, 2019 - Palo Alto US

Editorial This webinar will discuss how root cause is an essential part of a corrective action system and will provide some examples of how to perform root cause analysis. Objectives Reviewing CAPA The difference between Correction, Corrective Action and Preventive ...

Conference & Seminar: Management

Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries

Ref: 30381 Tuesday October 08th, 2019 - Palo Alto US

Editorial This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the ...

Conference & Seminar: Pharmacy

Recognizing and Responding to "Red Flags" in Clinical Operations

Ref: 30418 Tuesday October 08th, 2019 - Palo Alto US

Editorial Sponsors need to comply with various legal requirements for drug product development. These include communications with Federal and State Regulatory agencies. The post-marketing requirements include more functional areas of the company such as sales and marketing, medical affairs, and ...

Conference & Seminar: Hospital

Compliance Rules and Regulations for Hospital RN Case Managers, Social Work Case Managers, Case Management Leaders and Physician Advisors: ...

Ref: 30346 Wednesday October 09th, 2019 - Palo Alto US

Editorial This webinar will review the compliance issues that most greatly impact on your practice such as the 2-midnight rule, the NOTICE Act, HINNs, and many others. It will help you to identify where you may have compliance practice gaps as well as how to fix ...

Conference & Seminar: Management

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

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

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