World Conference Calendar

33841 Conferences

Health and Medicinerss


Applying ISO14971 and IEC62304 - A guide to practical Risk Management 2018

Applying ISO14971 and IEC62304 - A guide to practical Risk Management 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-29-2018 Last Day: 01-30-2018 Deadline for abstracts: 01-28-2018
Course "Applying ISO14971 and IEC62304 - A guide to practical Risk Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical devices in a…
21 CFR Part 11 Validation Checklist | Computer Systems Validation

21 CFR Part 11 Validation Checklist | Computer Systems Validation

Location: , United States
Category: Health and Medicine
Start Date: 01-25-2018 Last Day: 01-26-2018 Deadline for abstracts: 01-23-2018
Course "21 CFR Part 11 Compliance for Computer Systems Regulated by FDA" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability. FDA's 21 CFR Part 11 was enacted in the late 1990s and…
Complaints and Recalls | Complaint Handling System in Boston 2018

Complaints and Recalls | Complaint Handling System in Boston 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-25-2018 Last Day: 01-26-2018 Deadline for abstracts: 01-23-2018
Course "Complaint and Recall Management: A Compliant, Lean Program" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Complaint handling is likely one of the more cross-functional parts of your quality system: Customer Service may receive your customer complaints, Sales and Marketing may need to reach out to the customer for additional information, Regulatory Affairs may determine whether the complaint is reportable, QA may perform the root cause investigation, R&D or Manufacturing Engineering may need to be involved in the corrective action, and Quality Engineering may need to…
Verification vs. Validation - Product Process Software and QMS 2018

Verification vs. Validation - Product Process Software and QMS 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-22-2018 Last Day: 01-23-2018 Deadline for abstracts: 01-20-2018
Course "Verification vs. Validation - Product Process Software and QMS" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management. This course…
ESGAR Hands-on Workshop on CT Colonography, The Hague 2018

ESGAR Hands-on Workshop on CT Colonography, The Hague 2018

Location: , Netherlands
Category: Health and Medicine
Start Date: 03-14-2018 Last Day: 03-16-2018 Deadline for abstracts: 03-14-2018
The most renowned CT Colonography course in Europe, imitated by many. The only course where workstations of several vendors are simultaneously available. ESGAR CTC courses meet the requirements of radiological scientific societies requiring a certification of reading at least 50 endoscopically-controlled CTC cases. Participants will learn how to prepare a patient, how to conduct an examination and how to read a case. Live cases will be used for training on identification and characterisation of colonic cancers and polyps, including the most common pitfalls. Hands-on training is dedicated to the evaluation of diverticular disease, definition and significance of flat lesions, post-surgical…
What is the HIPAA Compliance | HIPAA Privacy Compliance Training 2018

What is the HIPAA Compliance | HIPAA Privacy Compliance Training 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2018 Last Day: 01-19-2018 Deadline for abstracts: 01-16-2018
Overview: This two-day seminar takes the participants through HIPAA compliance from start to compliance. The first presentation explains the history of HIPAA, why it came to being and its evolution. This covers what HIPAA is, what steps have to be performed to be HIPAA compliant and what HIPAA compliance is. It also provides definitions to key HIPAA terms, how to define a Business Associate and how to contract with Business Associates. The second part of the first presentation is an overview of how to manage the HIPAA compliance project. At the end of these presentations there will be a workshop…
FDA General Principles of Software Validation | Cyber Security 2018

FDA General Principles of Software Validation | Cyber Security 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2018 Last Day: 01-19-2018 Deadline for abstracts: 01-16-2018
Course "FDA's Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Software's level of complexity and use is expanding at exponential levels. Likewise, the potential risks to health follow suit. Ransomeware attacks hold your software hostage until you pay hundreds or thousands of dollars. Life supporting and life sustaining healthcare grinds to a halt. Extracting personal healthcare information is another plague that has a huge financial incentive for hackers. Your software is running on thin ice. The FDA looks…
Principal Investigator Responsibilities in Clinical Research | GCP 2018

Principal Investigator Responsibilities in Clinical Research | GCP 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2018 Last Day: 01-19-2018 Deadline for abstracts: 01-16-2018
Course "Onsite GCP Review and Update including the all-important 'Investigators Responsibility'" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This seminar is designed to acquaint all Participants with the Rules and Regulations that form the background of what is known as the GCP of Clinical Research. To follow "The Good Clinical Practices" (GCP) is to follow the standard for the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate and, most…
What is Computerized Testing Systems | GxP Compliance Testing 2018

What is Computerized Testing Systems | GxP Compliance Testing 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2018 Last Day: 01-19-2018 Deadline for abstracts: 01-16-2018
Course "A Risk Based Approach to Testing of Computerized GxP Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Testing is the science of identifying defects, so that they can be corrected, and of demonstrating that a system meets intended requirements. Testing computerized systems is considered a fundamental verification activity and appropriate testing is a regulatory expectation as described in many regulations e.g. EU GMP Annex 11. "Evidence of appropriate testing methods and test scenarios should be demonstrated. Particularly system (process) parameter limits, data limits and error…
Medical Device Software Risk Management Standard | Software Expert 2018

Medical Device Software Risk Management Standard | Software Expert 2018

Location: , United States
Category: Health and Medicine
Start Date: 01-18-2018 Last Day: 01-19-2018 Deadline for abstracts: 01-16-2018
Course "Medical Device Software: An Incremental Approach to Risk and Quality Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Engineers are dedicated to making things work, so a focus on how they might fail and harm someone can seem alien. Managing risk, however, is essential for all medical products- medical devices, including those involving software, have produced some painful examples of poor risk management with serious consequences. Experience has shown that there is a better way, that it is possible to manage risk in a changing…
What is Project Management in Pharmaceutical Industry Seminar

What is Project Management in Pharmaceutical Industry Seminar

Location: , United States
Category: Health and Medicine
Start Date: 01-15-2018 Last Day: 01-16-2018 Deadline for abstracts: 01-13-2018
Course "Risk Based Project Management for the Life Sciences Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Project management is a discipline that can be applied to all industries. In the pharmaceutical industry, project management is the key to addressing the unique regulatory, compliance and quality related needs of the industry. The process of clinical research and drug development, coupled with the critical issue of time to market, can use project management techniques to effectively apply scheduling, risk management, and comprehensive quality assurance and control to…
The Great Plains Laboratory Presents GPL Academy Practitioner Workshops

The Great Plains Laboratory Presents GPL Academy Practitioner Workshops

Location: , United States
Category: Health and Medicine
Start Date: 02-10-2018 Last Day: 02-11-2018 Deadline for abstracts: 02-09-2018
The Great Plains Laboratory, Inc. is pleased to bring you GPL Academy, a series of workshops designed to help practitioners learn how to integrate our comprehensive testing into their practices. When you attend a GPL Academy workshop, you will find out why our tests may be incredibly valuable to your practice, what particular markers may be the most meaningful to specific patients, and you will learn how to use our tests in tandem to provide your patients with the most personalized treatment plans possible. Day 1: Organic Acids Testing Workshop Learn how to use this comprehensive metabolic test in your…
Life Sciences Switzerland (LS2) Annual Meeting, Lausanne 2018

Life Sciences Switzerland (LS2) Annual Meeting, Lausanne 2018

Location: , Switzerland
Category: Health and Medicine
Start Date: 02-12-2018 Last Day: 02-13-2018
In the 2018 edition of the Life Sciences Switzerland (LS2) Annual Meeting, our four international plenary speakers will highlight their outstanding research in the field of Autophagy, the Nobel Prize winning topic. In addition, 10 scientific symposia from Physiology, to Systems Biology, Computational Biology, Neurosciences and Molecular Biosciences and more will present current research in their area. To complement the scientific program, career events for PhDs and Postdocs, contributions from 40+ industry partners, a transdisciplinary panel discussion on CRISPR/Cas9, an evening science crowdfunding event and award ceremonies will make this event unique for Switzerland! We again expect 600+ participants and…
Basic to Advanced Echo: Island Ultrasound

Basic to Advanced Echo: Island Ultrasound

Location: , United States
Category: Health and Medicine
Start Date: 09-27-2018 Last Day: 09-30-2018 Deadline for abstracts: 09-26-2018
The course will begin with a discussion of echocardiographic assessment of left and right ventricular function, including presentations on diastolic function and strain imaging for assessing myocardial function. We will then discuss a broad range of disease states for which echocardiography is useful, including ischemic heart disease, valvular heart disease, pericardial disease, and cardiomyopathies. The presentations will include basic concepts as well as advanced techniques including 3-D imaging and strain imaging. Throughout the course many cases will be presented. URLs: Website: https://go.evvnt.com/172247-1 Brochure: https://go.evvnt.com/172247-2 Prices: MD, PhD, DO, PharmD: USD 775 Fellows in Training, Sono, RN: USD 575 Time: 3:00…
Mental Health Strategies for First Responders

Mental Health Strategies for First Responders

Location: , Australia
Category: Health and Medicine
Start Date: 03-07-2018 Last Day: 03-08-2018 Deadline for abstracts: 03-07-2018
First responders are routinely exposed to higher levels of trauma, resulting in higher levels of stress. In order to reduce the risk of mental illness, strategies to increase awareness and build resilience must be implemented. Tackling the prevalent stigma that surrounds mental health for first responders will require a significant cultural change across the sector. The 2nd Annual Mental Health Strategies for First Responders national conference will provide emergency services with the necessary tools to continue improving their mental health programs, focusing on preventative approaches to build resilience while driving an organisational a wide cultural change. Key learnings: - Implement…
FDA Inspections: What Regulations Expect

FDA Inspections: What Regulations Expect

Location: , United States
Category: Health and Medicine
Start Date: 12-13-2017 Last Day: 12-13-2017 Deadline for abstracts: 12-13-2017
OVERVIEW In this 90 minute webinar attendees will gain an understanding of the parameters, approaches, and concerns of FDA inspectors, and the tools for preparing, coping, and managing those inspections in the pharmaceutical, biologics, and med device facilities. Other objectives include inspection authorities and processes including 483s, warning letters, recalls, and other potential actions, inspection processes, use of mock audits required documentation, formats, archiving, as well as how to respond to inspection and audit results. WHY SHOULD YOU ATTEND One should attend this webinar to increase one’s knowledge of FDA inspections, what inspectors are looking for and expect to see…
2nd Probiotics Congress: Europe

2nd Probiotics Congress: Europe

Location: , Netherlands
Category: Health and Medicine
Start Date: 03-21-2018 Last Day: 03-22-2018
The 2nd Probiotics Congress: Europe is set to take place on 21 – 22 March in Rotterdam, The Netherlands. Designed with scientists, researchers and businesses in mind, this meeting focuses on identification, product development and regulation. Leaders from academia and industry will present on topics across the vast field of dietary supplements, condensing it into two days of incisive presentations, roundtable debates and panel discussions. Further opportunities to network and form partnerships can be found at the co-located 5th Microbiome RandD and Business Collaboration Forum: Europe. Price Industry: EUR 999.00 Academic: EUR 599.00 Time: 9:00 am - 5:00 pm
Organic Process Research and Development Conference Florida 2018

Organic Process Research and Development Conference Florida 2018

Location: , United States
Category: Health and Medicine
Start Date: 03-05-2018 Last Day: 03-07-2018 Deadline for abstracts: 03-04-2018
At our Organic Process Research and Development conference, you will learn about improving efficiency and innovation in your synthetic route design, development and optimization. As it is increasingly vital for chemical and pharmaceutical companies to be able to effectively convert chemical reactions into manufacturing processes to run up to and beyond tonnage scale. Our conference will provide you with tools to keep you up-to-date in this dynamic field. Our hand-picked programme of presentations from key industry experts has been carefully selected to ensure that the most up-to-date issues are covered at this prestigious event. OPR and D conference will cover…
HIPAA and social media violations of HIPAA’s privacy requirements

HIPAA and social media violations of HIPAA’s privacy requirements

Location: , United States
Category: Health and Medicine
Start Date: 12-13-2017 Last Day: 12-13-2017 Deadline for abstracts: 12-13-2017
OVERVIEW This webinar educates the person attending about what rules govern HIPAA privacy that can be broken with a careless or untrained health care worker’s misuse of social media. While improper social media by an employee may get them fired, that same health care worker may lose his or her license to practice their chosen profession. This webinar covers the pitfalls that trap an unwary health care practitioner where patient confidentiality is breached when a violation of HIPAA privacy mandates occurs with the misuse of social media. The basic provisions of privacy for protected health information are well known as…
6th Plant Genomics and Gene Editing Congress: Europe

6th Plant Genomics and Gene Editing Congress: Europe

Location: , Netherlands
Category: Health and Medicine
Start Date: 05-14-2018 Last Day: 05-15-2018
Attracting experts working in all areas of plant science, the event will examine the latest in gene editing methods as well as exploring developments in NGS and omic technologies being used for progressing plant based research in aspects such as crop trait development, epigenetics, phenotyping, plant microbiome, and disease resistance as well understanding tools to overcome bottlenecks and enable successful data analysis and management. Price Industry Fee: EUR 999.00 Academic/Hospital/NFP Fee: EUR 599.00 Solution Provider Fee: EUR 1299.00 Time: on Monday May 14, 2018 at 9:00 am (ends Tuesday May 15, 2018 at 5:00 pm)

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