Medical meetings - Medical educations

Good Documentation Practice (GDocP) for FDA Regulated Industry

Ref: 30734 Monday December 16th, 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Good Documentation Practice (GDocP) for FDA Regulated Industry

Ref: 30742 Monday December 16th, 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Good Documentation Practice (GDocP) for FDA Regulated Industry

Ref: 31060 Monday December 16th, 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Handling OOS Test Results and Completing Robust Investigations

Ref: 30743 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they ...

What To Expect From FDA’s New Approach to Regulate Medical Software

Ref: 30744 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial The FDA’s emerging approach to medical software product regulation has important ramifications for patients, healthcare providers and insurers as well as product developers. So, it is critically important for companies throughout the life sciences and healthcare industries that ...

FDA: Mock and Pre-Approval Inspections (PAIs) - Part II

Ref: 30745 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This course for pharmaceutical professionals provides the information they require, to prepare for and understand what will happen during a mock audit and during a Pre-Approval Inspection (PAI).
  Objectives This course will provide you with the purposes of FDA’s ...

How to Conduct an Internal Harassment and Bullying Investigation to Determine Facts and Minimize Liability

Ref: 30895 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This webinar undertakes to explain the process of internal harassment and bullying investigation. Participants will learn how to handle harassment complaints and conduct the investigation to determine facts and minimize liability by analysing evidences, drawing conclusions, writing ...

Handling OOS Test Results and Completing Robust Investigations

Ref: 31061 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they ...

What To Expect From FDA’s New Approach to Regulate Medical Software

Ref: 31063 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial The FDA’s emerging approach to medical software product regulation has important ramifications for patients, healthcare providers and insurers as well as product developers. So, it is critically important for companies throughout the life sciences and healthcare industries that ...

FDA: Mock and Pre-Approval Inspections (PAIs) - Part II

Ref: 31065 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This course for pharmaceutical professionals provides the information they require, to prepare for and understand what will happen during a mock audit and during a Pre-Approval Inspection (PAI).
  Objectives This course will provide you with the purposes of FDA’s ...

Data Blocking and Patient Access of Medical Records under HIPAA - New Focus of Enforcement and Guidance

Ref: 31067 Tuesday December 17th, 2019 - Palo Alto ^US

Editorial This training program will provide a comprehensive look at the changes in the new access rights under HIPAA and CLIA regulations and prepare attendees for the process of incorporating the changes into how they do business in their facilities. It will also explain how the HIPAA audit ...

Protecting Your Company’s and Your Clients’ Rights with Restrictive Covenants, Non-Disclosure Agreements, Non-Competes, No-Solicitation and ...

Ref: 31052 Tuesday December 17th, 2019 - Aurora ^US

  OVERVIEW This webinar will introduce you to the procedures to protect confidential information, and through examples and recent case law explain how the clauses should be written, how they can best be enforced, and what are the legal pitfalls of misuse. Regarding the pitfalls of ...

Transforming an Organizational Culture into a Coaching Culture: How to Retain Your Millennial and Centennial Employees

Ref: 31057 Tuesday December 17th, 2019 - Aurora ^US

  OVERVIEW Establishing a Coaching Culture in the workplace may seem like a difficult task; this presentation provides a blueprint to implement a coaching culture at work to improve employee engagement and retain the Millennial and Centennial employees. WHY SHOULD YOU ATTEND Learn ...

Engaging and Retaining Top Talents with Stay Interviews: Strategize Employee Engagement Before It’s Too Late

Ref: 31035 Wednesday December 18th, 2019 - Aurora ^US

  OVERVIEW Job markets go up and down but one thing remains clear: companies want and need to retain their best performing employees. Unfortunately, most companies use the exit interview to collect reasons why their employees leave – an action that can be described by the old ...

Writing High-Impact Executive Summaries - How to Make a Positive Impression Using Smart Techniques

Ref: 31064 Wednesday December 18th, 2019 - Aurora ^US

  OVERVIEW An executive summary is simply a summary of summaries providing a concise summary of your current assignment to executives. This isn’t trial and error, since you only get one opportunity with executives to make a positive impression. This webinar discusses the key elements of ...

Enhancing Audit Advisory Practices

Ref: 30808 Wednesday December 18th, 2019 - Palo Alto ^US

Editorial Today’s Internal Audit groups are expected to do more than just assurance work. They are required to provide management with industry best practices, trends in risk management and perform advisory reviews of emerging and topical areas. This webinar introduces a new tool that helps ...

Tips on Dealing with Securities Regulatory Authorities - Audits, Etc.

Ref: 30965 Wednesday December 18th, 2019 - Palo Alto ^US

Editorial This webinar will discuss ways to effectively and efficiently deal with regulators, whether it be from an audit or other interaction. Regulators speak their own language and understanding this is imperative to building relationships and passing regulatory ...

I-9 Audits: Strengthening Your Immigration Compliance Strategies

Ref: 30974 Wednesday December 18th, 2019 - Palo Alto ^US

Editorial This webinar will help employers understand how to comply with the Form I-9 process, avoid fines for non-compliance, and understand key requirements to aid in efforts to maintain compliance. Objectives Mastering Form I-9 completion, storage, and retention ...

Stability Studies and Estimating Shelf Life

Ref: 31066 Wednesday December 18th, 2019 - Palo Alto ^US

Editorial In this webinar attendees will learn the useful methods and techniques for conducting a stability study and analyzing the resulting data for estimating shelf life. This webinar will provide the answers to help participants immediately apply the presented methods. The interpretation ...

How to Cultivate Employee Accountability: A Refined Approach to Performance Management

Ref: 31093 Wednesday December 18th, 2019 - Aurora ^US

  OVERVIEW Excuses. We’ve heard them all. Wouldn’t you love to see employee accountability in the workplace and have all your employees see what needs to be done, do what needs to be done and accept responsibility for the results? Unfortunately, such is often not the case. In this ...

Drug Manufacturing Inspection Part III

Ref: 30746 Thursday December 19th, 2019 - Palo Alto ^US

Editorial Attend this course to prepare for and understand what will happen during a Drug Manufacturing Inspection for Surveillance Inspections. It will explain the FDA criteria to perform a For Cause Inspection. Objectives This course will provide you with the system wide controls the FDA ...

Drug Manufacturing Inspection Part III

Ref: 30964 Thursday December 19th, 2019 - Palo Alto ^US

Editorial Attend this course to prepare for and understand what will happen during a Drug Manufacturing Inspection for Surveillance Inspections. It will explain the FDA criteria to perform a For Cause Inspection.
  Objectives This course will provide you with the system wide ...

New Employee Onboarding: The Roles and Responsibilities of HR and Management Beyond Handbooks, Benefits, and Photo IDs

Ref: 31039 Thursday December 19th, 2019 - Aurora ^US

  OVERVIEW Whether you call it New Employee Onboarding, Induction, Enculturation, or New Employee Orientation (NEO), the process used to welcome and train your new employees while capturing their excitement of a new job and reducing their new job jitters is critical to their success....

Strategizing Difficult Conversations: How to Communicate to Repair and Improve Working Relationships and Enhance Performance

Ref: 31083 Thursday December 19th, 2019 - Aurora ^US

  OVERVIEW For most managers, the toughest discussions involve providing repeat feedback when conducting annual performance reviews. These conversations can make you feel especially uncomfortable. However, when conducted properly, these sessions provide you with a great opportunity to ...

The Ins and Outs of I-9 and E-Verify: Best Practices to Avoid Steep Penalties

Ref: 31094 Thursday December 19th, 2019 - Aurora ^US

  OVERVIEW Immigration and Customs Enforcement (ICE) is not letting up. ICE has apparently resolved to continue auditing and inspecting employer compliance. Correctly completing a Form I-9, that seemingly simple form, involves sifting through gray areas and often conflicting ...