Health conference and seminar

Endocrine Update 2020 (February 24-28, 2020)

Ref: 30722 02/24/2020 -> 02/28/2020 - San Juan ^US

COURSE HIGHLIGHTS
•Case-based, interactive model that highlights multidisciplinary sessions in the evaluation and treatment of endocrine diseases, diabetes and obesity
•Clinically relevant education from experts in endocrinology, surgery, radiology and more
•Opportunities to interact ...

XXII Biennial Congress of the International Organization of Mycoplasmology

Ref: 30721 07/05/2020 -> 07/09/2020 - Tel Aviv-Yafo ^IL

It is our great pleasure to announce that the XXIII Biennial Congress of the International Organization for Mycoplasmology (IOM) will take place on July 5-9, 2020 in Tel Aviv, Israel.   The 23rd IOM meeting is an international conference that deals with all areas relating to Mollicutes ...

Wage and Hour Laws for Exempt and Nonexempt Employees: Understanding the Regulations and Employee Benefits

Ref: 30720 Friday November 15th, 2019 - Aurora ^US

 OVERVIEW Whether you’ve been managing employees for many years or you’re getting ready to manage a team, you need to understand the pay practices relevant and required for the type of employees you oversee. The two basic pay employee status types under federal and state laws are exempt ...

Stay Interviews: A Powerful Employee Engagement and Retention Tool

Ref: 30719 Tuesday November 12th, 2019 - Online

Get an in-depth understanding about stay interviews, their benefits, and how such interviews help in assessing the degree of employee engagement and retention tool.

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 ...

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 ...

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 ...

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 ...

The 7th Annual Arab International Paediatric Medical Congress

Ref: 30714 02/13/2020 -> 02/15/2020 - Dubai ^AE

The 7th Annual Arab International Paediatric Medical Congress, taking place in 13-15 February 2020, Dubai, UAE. The conference is aimed primarily at paediatricians.

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 ...

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 ...

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 ...

Developing Trust and Respect In the Workplace; Without Respect Work Environments Break Down!

Ref: 30710 Friday November 15th, 2019 - Aurora ^US

  OVERVIEW Workplace relationships are built on a foundation of trust and respect.  In this webinar you’ll learn how to establish your own personal credibility; you will get tips on building workplace respect, creating trust and a positive workplace atmosphere; you’ll understand ...

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 ...

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 ...

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 ...

2nd BD&L Summit For Life Sciences

Ref: 30706 03/10/2020 -> 03/11/2020 - San Francisco ^US

In order to effectively evaluate any new business development opportunities and ensure that the true value of a transaction has been realized, while forecasting the probability of both development and commercial success, life science companies need to ensure the right internal experts are ...

The Dubai International Nursing & Midwifery Congress

Ref: 30705 01/24/2020 -> 01/25/2020 - Dubai ^AE

  Nurses and midwives play a critical role in health promotion, disease prevention, and delivering primary and community care. They provide care in emergency settings and will be key to the achievement of universal health coverage.   The Dubai International Nursing & Midwifery ...

Human Error Reduction and Prevention: Implementing an Effective Program and Measuring Its Efficacy

Ref: 30704 Wednesday November 13th, 2019 - Aurora ^US

  OVERVIEW If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconvenience, you must do it because the regulation requires it. For example: the CFR - Code of Federal Regulations Title 21 Subpart B_Organization and Personnel ...

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 ...

Immuno-Oncology 360°

Ref: 30702 02/26/2020 -> 02/28/2020 - New York City ^US

The 6th annual IO360° Summit is the premier meeting across all stakeholders in IO, addressing the rapid advancements of clinical, scientific and business developments of IO in one setting to help develop therapeutics for a wider range of cancers at an accelerated rate. The 3 day summit features ...

The Middle East Pharma Cold Chain Congress

Ref: 30701 04/22/2020 -> 04/23/2020 - Dubai ^AE

The pharma sector in the MENA region has witnessed rapid development, which has been largely fueled by high population growth, increased life expectancy coupled with the prevalence of lifestyle-related diseases such as diabetes, aspiration for excellent healthcare services and the rising cost of ...

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 ...

ICSD 2020 : 8th International Conference on Sustainable Development, 9 - 10 September 2020 Rome, Italy

Ref: 30699 09/09/2020 -> 09/10/2020 - Rome ^IT

European Center of Sustainable Development in collaboration with Canadian Institute of Technology will organize the 8th ICSD 2020 International Conference on Sustainable Development, with particular focus on Environmental, Economic and Socio-Cultural Sustainability

The 2nd Middle East International Adult Vaccination Forum

Ref: 30698 03/02/2020 -> 03/03/2020 - Riyadh ^SA

  Over the years, vaccines have been known to prevent diseases in infants and children; while adult vaccination has an underestimated role in preventing diseases in communities. Adult Vaccination curb the risk of illnesses, disabilities, hospitalisation and even death that can follow viral ...