Why you should attend:
Promotes safety culture through peer training.
Training is intended to be participatory, using hands-on activities.
Outreach training content includes hazard recognition and avoidance, workers' rights, employer responsibilities, and how to file a complaint; it emphasizes the value of safety and health to workers, including young workers.
Participants receive a participation card from the US Department of Labor.
Areas Covered in the Session:
Introduction to OSHA
Walking and Working Surfaces, including fall protection
Exit Routes, Emergency Action Plans, Fire Prevention Plans, and Fire Protection
Electrical
Personal Protective Equipment
Hazard Communication
Machine Guarding.
Safety and Health Program.
Fall Protection.
Hazard Communication.
Who Will Benefit:
Safety Managers
HR Managers
Safety Committee Members
Production Supervisors
Production Foreman
Production Managers
Plant Managers
Maintenance Personnel
Maintenance Manager
New hired employees
Production Line employees
Design Engineers
Operations Managers
Occupational Safety Trainers
Agenda:
Day 1 Schedule
(8:00-8:30 am):
Registration & Meet and Greet.
Lecture 1 (8:30-9:30 am):
Introduction and Presentation Overview
Instructor & Participation Introductions
Listing of Participants Goals
Seminar Objectives
Defining Safety
Lecture 2 (9:30-10:00 am):
An Introduction To OSHA
The 2 Hands of OSHA
Employee & Employer Rights & Responsibilities
State and Federal Jurisdictions
(10:00-10:15 am) Break
Lecture 3 (10:15-11:15 am):
An Introduction To OSHA
Workplace Injury Reporting and Recording Requirements
Volks Decision and Current Changes of Decision
Temporary & Contract Employee Emphasis Program
Fatality Reporting Time Requirements
Lecture 4 (11:15- Noon):
OSHA Reporting Definitions
Amputation, Loss of an Eye Reporting Time Requirements
In-Patient Hospitalization Reporting Time Requirements
OSHA's Definition of In-Patient Hospitalization
OSHA's Definition of Amputation
OSHA's Definition of Loss of an Eye
Citation Review of Non Reporting Cases
(Noon - 1:00 pm) Lunch
Lecture 5 (1:00-2:00 pm):
Final Rule to Improve Tracking of Workplace Injuries & Illnesses
History that lead to new rule and major provisions of it.
Why employers are required to submit electronically injury and illnesses on OSHA secured website.
How the new requirement impacts businesses.
Who is to submit and how to submit electronically.
Compliance schedule of submitting injury and illnesses on OSHA secured website.
(2:00-2:15pm) Break
Lecture 6 (2:15-3:15pm):
Injury and Illness Reporting and Disciplinary Action Provision
Fairfax Memo
Discuss how OSHA will determine if employer procedures are "reasonable" for having employees report injury and illnesses.
Discuss how OSHA will determine if employer procedures are "reasonable" for disciplinary action of late reporting.
Why the new provision?
(3:15-3:30pm) Break
Lecture 7 (3:30-4:00pm):
Examples of Reasonable Illness Reporting Procedures and Disciplinary Actions
Participants Procedural Exercise
Lecture 8 (4:00-4:30pm):
Summary of Day 1
Summary of today's topics
Q&A
Tomorrow's Agenda
Day 2 Schedule
(8:00-8:30 am):
Registration & Meet and Greet.
Lecture 1 (8:30-9:30 am):
Incentive Program & Post Injury and Illness Drug Testing Provision
Discuss OSHA's "reasonable" requirements of an incentive program.
Discuss OSHA's "reasonable" requirements of post injury and illness drug testing program.
Why the new provision?
Compliance Schedule
(9:30-9:45am) Break
Lecture 2 (9:45-11:00 am):
Incentive Program & Post Injury and Illness Drug Testing Provision
Incentive Program Procedural Exercise and Discussion.
Post Injury & Illness Drug Testing Procedural Exercise and Discussion.
State Law, Federal Law & OSHA.
(11:00 am-11:15am) Break
Lecture 3 (11:15-Noon):
Employees Right To Report Injuries & Illnesses Free of Retaliation Provision
Review 11c - Whistleblower Protection Changes
(Noon - 1:00 pm) Lunch
Lecture 4 (1:00-2:00pm):
Employees Right To Report Injuries & Illnesses Free of Retaliation Provision
Discuss OSHA's new enforcement process pertaining to the Whistleblower Protection Legislation and how it impacts business.
Discuss how to comply with OSHA's "reasonable" requirements for informing employees about their rights to report injuries and illnesses.
New OSHA poster
(2:00-2:15pm) Break
Lecture 5 (2:15-3:15):
Participant Exercise - Procedural Writing & Discussion
(3:15-3:30pm) Break
Lecture 6 (3:30-4:00pm):
Current Changes, OSHA Guidelines & Trump Administration
Lecture 7 (4:00-4:30pm):
Summary of Day 2
What Did You Learn?
Final Q&A
Feedback
Speaker:
Michael Aust
Senior Safety Specialist, OSHA Consultant & Trainer, 1030 Communications Group, LLC
Michael Aust is a safety professional with over 22 years of experience managing OSHA regulatory and training compliance. Mr. Aust has a Master of Science in Occupational Safety, Health and Environmental Management and also served as the management representative for various safety and environmental management systems throughout his career. Since 2000, Michael has been an Authorized OSHA Outreach Instructor for both General and Construction Industry and is a content contributor for various safety consultation and industry newsletters.
Michael has provided safety management expertise and regulatory compliance to a variety of industries since 1995. His extensive experience in the safety and health field has been earned from working in a variety of different types of organizations within the private sector. He has developed and implemented safety management systems for organizations without such processes and has helped mature management systems for Fortune 50 and Fortune 100 companies.
Location: San Diego, CA Date: September 18th & 19th, 2018 and Time: 8:00 AM to 5:00 PM
Venue: DoubleTree by Hilton San Diego Downtown 1646 Front St, San Diego, CA 92101, USA
Price:
Register now and save $200. (Early Bird)
Until August 10, Early Bird Price: $1,295.00
From August 11 to September 16, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901798SEMINAR?seo
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San Diego Seminar on OSHA 10 Hour General Industry Course
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Seminar on Software Risk Management in Philadelphia
Description:
The seminar will address the specific challenges software poses for the risk management process. Basic risk management concepts will be introduced and then applied to software specific applications.
Why you should attend:
Risk Management is a regulatory and statutory requirement for medical devices. The generic procedure to perform risk management is outlined in ISO14791, however, as soon as software is used challenges arise. How to address these specific software issues and the application of FDA and IEC requirements for development of safety-critical software used in medical devices is the content of this seminar.
Who Will Benefit:
Project managers
Software Engineerrs
Regulatory specialists
Quality assurance specialists
Documentation specialists
Test managers
Software team leaders and lead developers
Agenda:
Day 1 Schedule
Lecture 1 (90 Mins):
Legal and regulatory requirements for risk management
Risk management and quality systems
Lecture 2 (90 Mins):
Risk Management Basics
What are hazards / hazardous situations
Hazard characteristics
Risk and risk rating
Residual risk
Lecture 3 (90 Mins):
Software failures
Random and systematic faults
Fault control means
Software failure effects
Lecture 4 (90 Mins):
System Architectures
Software Architecture
Software Tools and Methods
Multiprocessor systems
Real-time challenges
Day 2 Schedule
Lecture 1 (90 Mins):
Software Criticality Classification
IEC criticality classed
FDA level of concern
Lecture 2 (90 Mins):
The 62304 Development Process
Life Cycle
Documentation
Comparison to FDA requirements
Lecture 3 (90 Mins):
Software Risk Management
Software Configuration Management
Software Problem Resolution
Software Maintenance
Lecture 4 (90 Mins):
Legacy Software
Risk-based verification
Third-party software (SOUP, COTS)
Speaker:
Markus Weber
Principal Consultant, System Safety Inc.
Markus Weber, Principal Consultant with System Safety, Inc., specializes in safety engineering and risk management for critical medical devices. He graduated from Ruhr University in Bochum, Germany with a MS in Electrical Engineering. Before founding System Safety, Inc., he was a software safety engineer for the German approval agency, TUV. Since 1991, Mr. Weber has been a leading consultant to the medical device industry on safety and regulatory compliance issues, specifically for active and software-controlled devices. In conjunction with the FDA, he has published works on risk management issues and software-related risk mitigations. Mr. Weber has helped multiple companies, from startups to Fortune 500 firms.
Location: Philadelphia, PA Date: September 24th & 25th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: DoubleTree by Hilton Philadelphia Airport 4509 Island Avenue, Philadelphia, PA 19153
Price:
Price: $1,495.00 (Seminar Fee for One Delegate)
Register for 5 attendees Price: $4,485.00 $7,475.00 You Save: $2,990.00 (40%)*
Register for 10 attendees Price: $8,222.00 $14,950.00 You Save: $6,728.00 (45%)*
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901822SEMINAR?seo
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Statistics for Process and Quality Control
Description:
This 2-day seminar includes the steps and techniques used to quantify variability in manufacturing processes, and to assure quality products.
The concepts and information presented will be mainly concerned with statistical quality control: obtaining information (data) that is objective, unbiased, and useful for decision making. An emphasis will be placed on the set-up and use of control charts and acceptance sampling systems and procedures.
The objective of the seminar is to provide information that can be used immediately by personnel involved in production operations, and by supervisors and management in decision making. Although the presentation involves use of statistical techniques, presentation of statistical theory will be limited to only what is needed by the attendees to understand and implement processes and testing within the statistical framework.
Presented examples will include an emphasis on the manufacturing processes and quality assurance needs of personnel in the medical device and pharmaceutical industries.
Process and quality control are constantly evolving. Therefore, historical concepts, current trends and regulatory requirements will be discussed. The presentation of statistical charts and analyses, graphical techniques for planning, trouble-shooting and problem solving will also be presented.
Why you should attend:
All processes exhibit intrinsic variation. However, sometimes the variation is excessive and this hinders the ability to achieve reliable measurements and desired results. Statistical process control (SPC) and statistical quality control (SQC) allow us to control the functions of our processes (input) and the quality of our product (output) by providing tangible tools for monitoring and testing.
Process and quality control is important for a companys reputation. A good system of processing and quality checks reduce costs associated with production waste and re-work due to defects, and allows a company to deliver products that are high in quality. Many industries are also required to have a good quality management system in place to achieve compliance with regulatory authorities.
This seminar will provide attendees with the statistical tools necessary to monitor processes and test the quality of manufactured product. Ms. Eisenbeisz will make use of Minitab software in her presentation.
Areas Covered in the Session:
FDA QSR, ISO 13485:2016, IS 9001:2015 regulations and harmonization
Overview of statistical theory and nomenclature for processes and quality control
Variability and risk assessment in practice
Control before testing!
Which chart for which process?
Setting statistical specifications, control limits, and signals
Who will benefit:
Quality Assurance (QA) Engineers
Quality Control (QC) Engineers
R&D Engineers
Process Control Personnel
Manufacturing/Industrial Personnel
Production Supervisors
Management Personnel of Processing Facilities
Agenda:
Day 1 Schedule
Lecture 1 (90 Mins): It's a System! Elements of Quality Management
Deming 14 points for total quality management
Dr. Ishikawa, seven quality control tools (7-QC) and supplementals (7-SUPP)
Pareto principle (80/20 rule)
Shewhart (Plan, Do, Study, Act)
Lecture 2 (90 Mins): Regulatory Requirements in Quality Management
FDA Quality System Regulation (QSR)
ISO 13485:2016
IS 9001:2015
Harmonization of regulations with FDA guidance/regulations
Lecture 3 (90 Mins): Statistical basics
Check sheets/tally sheets
Descriptive statistics
Binomial Distribution (discrete data)
Hypergeometric Distribution (sampling without replacement)
Normal Distribution (continuous data)
Lecture 4 (90 Mins): Statistical Basics (cont'd)
Graphical Techniques:
o Histograms
o Scatterplots
o Pareto charts
o Cause and effect (fishbone) diagrams
o Defect concentration diagrams
Day 2 Schedule
Lecture 1 (90 Mins): Statistical Process Control: The ABC's of Control Charts
Elements of a control chart
Control Charts for Discrete Data
o c chart
o u chart
o p chart
o np chart
Control Charts for Continuous Data
o X-bar chart
o R chart
o I chart
o MR chart
o Combined charts (Xbar-R, I-MR)
Lecture 2 (90 Mins): Statistical Process Control (cont'd)
More Control Charts
o Classical Shewhart control charts
o Cumulative Sum (CUSUM) charts
o Exponentially Weighted Moving Average (EWMA) charts
o Hotelling (multivariate) control charts
Lecture 3 (90 Mins): Statistical Quality Control - Attribute Sampling Plans
C= 0 /Zero Acceptance
Single sample plan
Double-sampling plan
Multiple sampling plan
Sequential sampling plan
Skip-lot sampling plan
Lecture 4 (90 Mins): Statistical Quality Control - Variables Sampling Plans
Sampling size and critical distance
Known vs. unknown standard deviation
One or two specification limits
Using ANSI Z1.9
Speaker:
Elaine Eisenbeisz
Owner and Principal Statistician, Omega Statistics
Elaine Eisenbeisz, is a private practice statistician and owner of Omega Statistics, a statistical consulting firm based in Southern California. Elaine has over 30 years of experience in creating data and information solutions for industries ranging from governmental agencies and corporations, to start-up companies and individual researchers.
Location: San Diego, CA Date: September 18th & 19th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: DoubleTree by Hilton San Diego Downtown 1646 Front St, San Diego, CA 92101, USA
Price:
Register now and save $200. (Early Bird)
Until August 10, Early Bird Price: $1,295.00
From August 11 to September 16, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901753SEMINAR?seo
Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/
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Tougher Import Rules for FDA Imports in 2018
Description:
Background:
FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an import and export program find their shipments delayed, detained or refused. As of December 2016, FDA and CBP officially implemented the Automated Commercial Environment (ACE) entry filing system. You either meet ACE requirements or face entry refusals and monetary penalties of up to $10,000 per offense. Other factors can derail the expectation of a seamless import entry process. The course covers detailed information about the roles and responsibilities of the various parties involved with an import operation and how to correct the weakest link(s) in the commercial chain. The course will include tips on how to understand FDA's thinking, negotiate with the FDA and offer anecdotal examples of FDA's import program curiosities.
Why you should attend:
What happens when your product is detained? FDA will begin a legal process that can become an expensive business debacle. You must respond fully within short timeframes. This is not the time for you to be on a learning curve. You need to have a plan in place and know what you are doing.
The FDA is steadily increasing the legal and prior notice information requirements. If you do not know what those requirements are and you initiate a shipment, your product is figuratively dead in the water. You must be accurate with the import coding information and understand the automated and human review process. If not, you can expect detained shipments. CBP is implemented a new "Automated Commercial Environment" computer program that changes import logistics and information reporting for FDA regulated products. Your shipment may be stopped before it is even loaded at the foreign port.
When products are refused, you have different options. Some options may cost more than others. For example, your product can be seized and destroyed by the government. You may be fined if you do not act in a timely manner. These are common problems that become prohibitively expensive. You should know how to avoid common problems or at least how to mitigate the cost by using established and effective business planning.
Learn how to deal with common problems, such as returns for repair, importing QC samples, and investigational products
On a positive note, the FDA is implementing the Voluntary Qualification Importer Program under the FDA Food Safety and Modernization Act. One other perk is that FDA offers export certificates, for a modest fee, which may give you a competitive advantage in foreign markets. In some cases, a FDA export certificate is required by foreign governments. Finally, the new EU Medical Device Regulation will change how FDA manages foreign inspections and in your favor.
Who Will Benefit:
Domestic importers
Foreign exporter
Initial importers
International trade executives
Venture Capitalists
Marine insurance underwriters
Import Brokers
Regulatory affairs managers
Import / Export consultants
In-house counsel
Contract specialists
Logistics managers
Third party establishment inspection entities
Sales managers
Investors
Agenda:
Day 1 Schedule
Lecture 1:
FDA Legal Authority Customs and Border Control (CBP) Import Process FDA Import Process Registration and documentation
Lecture 2:
FDA Import Process (continued)
Import Brokers
Prior Notice Information
CBP and FDA computer programs
Import Codes
Bonds and Bonded Warehouses
FDA "Notice of Action"
Lecture 3:
Import Delays Import Alerts Detention Refusals
Day 2 Schedule
Lecture 1:
Foreign Inspections FDA 483 - Inspectional Observations
Lecture 2:
FDA Warning Letters and Automatic detention
Lecture 3:
Import Hypothetical FDA Import for Export Program FDA Export Program Export Hypothetical
Lecture 4:
FDA Export Program Special Import Issues
Trade Shows
Personal Use
Compassionate Use
Speaker:
Casper Uldriks
ex-FDA Expert and former Associate Center Director of CDRH
Casper (Cap) Uldriks owns Encore Insight LLC, which provides consulting services on FDA Law. He brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and as an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. He is recognized as an exceptional and energetic speaker. His comments are candid, straightforward and of practical value. He understands how FDA thinks, operates and where it is headed.
Location: Boston, MA Date: September 13th & 14th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: Four Points by Sheraton Boston Logan Airport Revere, MA 407 Squire Rd, Revere, Massachusetts 02151, United States
Price:
Register now and save $200. (Early Bird)
Until August 10, Early Bird Price: $1,695.00
From August 11 to September 11, Regular Price: $1,895.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901405SEMINAR?seo
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Understanding the HIPAA/HITECH Requirements | Washington Seminar
Description:
This one-day seminar will get into the fine details of what we need to do and how to do it.
We will go point by point through the entire HIPAA Security Rule and uncover simple methods to comply and create policy.
The primary goal is to ensure everyone is well educated on what is myth and what is reality with this law, as there is so much misleading information regarding the do's and don'ts with HIPAA. I want to add clarity for compliance officers.
It will also address major changes under the Omnibus Rule and any other applicable updates for 2018.
Why you should attend:
Omnibus has changed the HIPAA landscape for good!
Do you know all of the requirements of this enigmatic law?
Are you abiding by them?
My goal is to make this extremely complex enigma known as "HIPAA" very easy to understand with a painless step by step approach to an otherwise harrowing task... Times have changed and new laws are now in place concerning Protected Health Information. The best way to protect your practice or business and save yourself future headaches and possible litigation or Federal fines is to be proactive instead of reactive.
This once rarely enforced law has changed and you need to know what's going on!
Protect your practice or business!
These day's trial attorney's pose an even higher risk than the Federal government!
State laws are now in place increasing liability for patient remedies!
What factors might spurn a lawsuit or a HIPAA audit? ...are you doing these things?
Why are the Feds enforcing after all these years?
We will be discussing 2018 changes taking place in Washington with the Health and Human Services in regards to the enforcement of the HIPAA laws already on the books as well as some detailed discussions on the audit process as well as some current events regarding HIPAA cases (both in courtrooms and from live audits)
Areas Covered in the Session:
Study all 18 Standards and 44 Implementation Specifications of the regulations
Updates for 2018
Requirements of Compliance Officers
New definition of what constitutes protected health information
Real life litigated cases
BYOD
Portable devices
Business associates and the increased burden
Emailing of PHI
Texting of PHI
Federal Audit Process
HIPAA and suing - how this works
Risk Assessment
Who Will Benefit:
Practice managers
Any business associates who work with medical practices or hospitals (i.e. billing companies, transcription companies, IT companies, answering services, home health, coders, attorneys, etc)
MD's and other medical professionals.
Agenda:
Lecture 1 (90 Mins):
HIPAA: a Brief History
New definition of what constitutes Protected Health Information
HIPAA and the Business Associate
Lecture 2 (90 Mins):
Through examination of all 18 Standards and 44 Implementation Specifications of the HIPAA Security Rule and how to apply them
How to enforce policy for each standard and implementation specification
Lecture 3 (90 Mins):
The Federal Audit Process and things to be ready for
HIPAA and Suing - how this works and examples of real cases
Technology and HIPAA - best practices and big "no-no's"
HIPAA Texting and Emailing - myth vs reality
Lecture 4 (90 Mins):
Review once more all standards
Speaker:
Brian L Tuttle
Brian L Tuttle, CPHIT, CHP, CHA, CBRA, CISSP, Net+
Nationally Renowned Compliance Consultant12
Brian L Tuttle is a Certified Professional in Health IT (CPHIT), Certified HIPAA Professional (CHP), Certified HIPAA Administrator (CHA), Certified Business Resilience Auditor (CBRA), Certified Information Systems Security Professional (CISSP) with over 18 years' experience in Health IT and Compliance Consulting.
Location: Washington DC Date: September 10th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: Courtyard Arlington Crystal City/Reagan National Airport 2899 Jefferson Davis Hwy, Arlington, VA 22202, USA
Price:
Until July 31, Early Bird Price: $649.00
From August 01 to September 08, Regular Price: $849.00
Register for 5 attendees Price: $1,947.00 $3,245.00 You Save: $1,298.00 (40%)*
Register for 10 attendees Price: $3,569.00 $6,490.00 You Save: $2,921.00 (45%)*
Register now and save $200. (Early Bird)
Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com
Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901783SEMINAR?seo
Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/
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Otolaryngology Conferences | ENT Meetings | Otorhinolaryngology 2018
EuroSciCon Ltd. expanded with the support from scientific societies and opens its arm to conduct global medical and healthcare meetings. EuroSciCon is proud to announce its 7th Edition of International Conference on Otorhinolaryngology organized around the theme An Insight into the Recent Advances in Otolaryngology to be held amid December 13-14, 2018 at Madrid, Spain.
The "Otorhinolaryngology-2018 plays host for the Multinational organizations, entrepreneurs across the globe, the researchers and academicians. Prominently ENT Surgeons/Specialists/Consultants; Neurotologists; Otolaryngologists; ENT Departments; General Practitioners; Specialists Academia and others who stay plunged in learning and practice of the science of Otolaryngology and also the Entrepreneurs, business delegates from otolaryngology enterprises, sponsors and exhibitors over the globe to share their most recent advances and procedures guaranteeing great well-being and the disposal of impeding, lethal and intellectual illnesses of humanity. Through this the abstracts and research profiles of our speakers and organizing committee members getting global visibility which is an additional feature that you would be receiving while networking opportunities before, during and after the conference.
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Mayo Clinic Endocrine Update 2019
Designed for endocrinologists and interested internists and surgeons, Endocrine Update addresses gaps in medical knowledge and barriers in clinical practice to improve the outcomes of patients with endocrine and metabolic disorders. Topics span the full range of endocrinology through lectures, debates, panel discussions, clinicopathologic sessions, clinical pearls sessions, informal breakfast roundtable discussions and small-group discussions with experts. Attendees have plenty of opportunity for interaction with the course faculty.
-Case-based, interactive model that highlights multidisciplinary sessions in endocrine diseases and endocrine cancers, laboratory testing, disorders of calcium and bone, diabetes and obesity
-Interactive tumor board sessions, with opportunities for case submissions from attendees
-Opportunities to interact with course faculty during breakfast roundtable discussion and small group discussions
-Apply what you learn immediately into your practice
-New! Access to course recordings after the course
Tumor Board Submissions
We invite you to take advantage of a unique opportunity and be a presenter at our Oncology Board Sessions held on Monday February 1st and Wednesday February 3rd!
Participants are encouraged to submit a case that presents a diagnostic and/or therapeutic challenge in the management of endocrine tumors and/or cancers (thyroid, neuroendocrine) to a panel of experts. Our experts represent the fields of Endocrinology, Surgery, Pathology and Oncology. Our panelists will share their expertise and unique insights about your case. We are confident this session will be a great learning opportunity for all. Cases can represent a broad range of common and/or uncommon endocrine tumors, such as cytology of thyroid nodules or questions on the management of metastatic thyroid cancers or adrenal tumors.
Please see website for learning objectives and credit details - ce.mayo.edu/endo2019
Tickets: https://go.evvnt.com/250454-1?pid=154
Time: 06:30 to 12:30
Prices:
Full Fee: MD, DO, Scientist: USD 1099.0,
Reduced Fee: Resident, Fellow, NP, PA, Allied Health Professional, Retired: USD 950.0
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Athens 22nd International Conference on Medical, Medicine and Health Sciences (MMHS- 2018 Athens)
Advances in collaborative research for public Health, Medical and Medicine Sciences for better healthcare services to society
The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe
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Athens 23rd International Conference on Medical, Medicine and Health Sciences (MMHS- 2018 Athens)
Advances in collaborative research for public Health, Medical and Medicine Sciences for better healthcare services to society
The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe
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Athens 26th International Conference on Medical, Medicine and Health Sciences (MMHS- 2019 Athens)
Advances in collaborative research for public Health, Medical and Medicine Sciences for better healthcare services to society
The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe
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Athens 27th International Conference on Medical, Medicine and Health Sciences (MMHS- 2019 Athens)
Advances in collaborative research for public Health, Medical and Medicine Sciences for better healthcare services to society
The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe
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Athens 29th International Conference on Medical, Medicine and Health Sciences (MMHS- 2019 Athens)
Advances in collaborative research for public Health, Medical and Medicine Sciences for better healthcare services to society
The conference will cover vital issues in medical, medicine and health sciences under multiple sub-themes. The aim of our conference is to support, encourage and provide a platform for networking, sharing, publishing and nurturing the potential growth of individual scholars across the globe
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CannaTech: Cannabis Innovation Summit
LONG DESCRIPTION OF EVENT:
CannaTech is a high-level conversation engineered to accelerate change in this industry.
Our CannaTech Tel Aviv flagship event will address the unique challenges that currently face the global medical cannabis market and offer practical steps needed to push government and industry forward in policy and practice.
We provide two full days of educational content, delivered in short TED-style segments with a sharp focus on investment, research, agtech, innovation, and regulatory issues within the global cannabis market. We will give you an economic global round up, shine the light on new innovation, address cannabis as medicine, cover the importance of tech transfer, and much more.
CannaTech is an expertly executed event experience that offers high-level networking and evidence-based information that challenges the status-quo of the medical cannabis industry. We also create unprecedented opportunity for deal flow.
THIS ISN'T JUST AN INCREDIBLE EVENT, THIS IS THE FUTURE OF CANNABIS
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CannaTech: Cannabis Innovation Summit
LONG DESCRIPTION OF EVENT:
CannaTech is a high-level conversation engineered to accelerate change in this industry.
Our CannaTech Tel Aviv flagship event will address the unique challenges that currently face the global medical cannabis market and offer practical steps needed to push government and industry forward in policy and practice.
We provide two full days of educational content, delivered in short TED-style segments with a sharp focus on investment, research, agtech, innovation, and regulatory issues within the global cannabis market. We will give you an economic global round up, shine the light on new innovation, address cannabis as medicine, cover the importance of tech transfer, and much more.
CannaTech is an expertly executed event experience that offers high-level networking and evidence-based information that challenges the status-quo of the medical cannabis industry. We also create unprecedented opportunity for deal flow.
THIS ISN'T JUST AN INCREDIBLE EVENT, THIS IS THE FUTURE OF CANNABIS
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Antibody Engineering and Therapeutics
Antibody Engineering and Therapeutics is the #1 forum for scientific exchange and networking in the fields of antibody engineering and therapeutics, immunobiology and next-generation binders.
For over 25 years, renowned academic and industry scientists from around the world have convened to share best practices and scientific results to accelerate antibody research, discovery efforts and clinical programs.
With 900+ attendees, 135+ speaker presentations and 75+ exhibitors and 135+ scientific posters focused on antibody science and technology
For more information or to register, visit: www.AntibodyEng.com.
URL:
Tickets: https://go.evvnt.com/250507-1?pid=154
Prices:
Industry Rate for 4-Day Conference: USD 2699.0
Academic/Government Rate for 4-Day Conference: USD 1099.0
Industry Rate for Full-Day Pre-Conference Workshop: USD 899.0
Government/Academic Rate for Full-Day Pre-Conference Workshop: USD 599.0
Industry Rate for Half-Day Pre-Conference Workshop: USD 499.0
Academic Rate for Half-Day Pre-Conference Workshop: USD 299.0
Speakers: Rachael Clark, MD, PhD Shing-Yiu Yip and Cecilia M. Hepp Associate Professor of Dermatology at Harvard Medical School, Bahija Jallal, PhD President, Medimmune and Executive Vice President, AstraZeneca at Medimmune and AstraZeneca, David Baker, PhD Professor of Biochemistry at University of Washington, Sally Ward, PhD Professor, Department of Molecular and Cellular Medicine at Texas AandM University Health Science Centre and Centre for Cancer Immunology and University of Southampton
Time: 8:00 am to 5:00 pm
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UCSF TRANSPLANT 2018: PIONEERING ADVANCES IN TRANSPLANTATION
Plenary sessions include the future of transplantation, the changing transplant population, management of post-transplant infections, and other contemporary and controversial topics. Specific clinical tracks will focus on current issues and patient management strategies appropriate for each area of specialization.
URLs:
Brochure: https://go.evvnt.com/250495-0?pid=154
Tickets: https://go.evvnt.com/250495-2?pid=154
Prices:
Practicing Physicians: USD 400.0,
Nurses/Pharmacists/ Allied Health Professionals/ Residents/Fellows: USD 300.0
Time: 7:00 am to 4:30 pm
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Xcelerate @ Biotech Week Boston
Be a part of the Biotech Week Boston ecosystem and register for an Xcelerate pass. This popular program taking place September 5-6, 2018 in Boston includes spotlight keynotes, a startup pitch competition, access to the Biotech Week Boston poster and exhibit hall, and numerous networking opportunities. If you care about life sciences and the people and issues driving the future, then you won't want to miss this event. Learn More About Xcelerate.
URL:
Tickets: https://go.evvnt.com/250504-1?pid=154
Time: 2:45 pm to 9:00 pm
Price:
Xcelerate Pass: USD 449.0
Speakers: Jerome Adams, US Surgeon General, US Department of Health and Human Services, Bob Langer, Institute Professor, MIT, Elizabeth Nabel, President, Brigham Health, George Yancopoulos, President and Chief Scientific Officer, Regeneron Pharmaceuticals, Amy Schulman, Co-Founder and CEO, Lyndra; Partner, Polaris Partners, Susan Hockfield, President Emerita and Professor of Neuroscience, MIT, Alexis Borisy, Partner, Third Rock Ventures; Chair, National Venture Capital Association
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HOA Vista India
This 3-day congress and exhibition is filled with lectures from esteemed local and international experts in the fields of Ophthalmology and Optometry, all willing to share knowledge and up-to-date practices used globally.
The attending delegates will receive the best of scientific content both in theory and practical pearls to further refine their professional skills in their practice.
In addition, participants will have access to the B2B networking platform that will enable interested parties to set up meetings with potential future partners and collaborators.
Highlights
3 Day Exhibition: 16-18 NOVEMBER 2018
3 Day Conference: 16-18 NOVEMBER 2018
This event is under the auspices of Hyderabad Ophthalmologists Association
This event is intended to be a State-of-the-Art Academic Feast with a blend of Practical Science and camaraderie with fraternity and friends
Around 700 delegates apart from trade fraternity is expected to participate
Interactive sessions during the International Conference
Business Networking that can lead to relevant referral businesses
A great opportunity to exhibit and demonstrate the products directly
Topics
Basic sciences and Optometry
Glaucoma
Refractive Surgery
Neuro-Ophthal
Surgical Complications
Challenging Cases
Cataract
3D oculoplasty show
Cornea
Pediatric ophthalmology
Competitive video and free paper presentations
For more information about the program, please do not hesitate to visit the site : http://vista-congress.com/scientific-program/ or to contact our local representatives: Pradeep Bandari - pradeepb@kenes-exhibitions.com.
URLs:
Tickets: https://go.evvnt.com/251169-1?pid=154
Website: https://go.evvnt.com/251169-3?pid=154
Prices:
Early bird registration: USD 100.0
Onsite registration: USD 125.0
Optometrists/ Postraduate Students / Vision Scientists early registration: USD 80.0
Time: 9:00 am to 6:30 pm
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4th World Congress on Parkinsons &Huntington Disease
The present Parkinsons Congress focuses on Neuromuscular Disorders occurs due to loss of communication between neurons in the brain. These disorders are noted as the greatest threat to humans in present generations around globe. More than Hundred diseases are in association with nervous system including Parkinson's disease they are Alzheimer's disease, brain tumors, Multiple Sclerosis Amyotrophic Lateral Sclerosis, Spinal Muscular Atrophy, Stroke and Epilepsy.
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Psych Congress 2018
Psych Congress serves as a unique, integrated forum to connect members of the entire mental health team psychiatrists, physician assistants, nurse practitioners, psychologists, primary care physicians, and other mental health professionals with the foremost experts in mental health to improve patient outcomes through education. No other mental health conference offers this level of practical education combined with state-of-the-art treatment approaches and emerging research findings.
URLs:
Brochure https://go.evvnt.com/249711-2?pid=154
Inquiries https://go.evvnt.com/249711-3?pid=154
Speakers: Rakesh Jain, MD, MPH, Charles Raison, MD, Vladimir Maletic, MD, Anna Lembke, MD, Robin Carhart-Harris, PhD, David Granirer, RPC, MPCC, MSM, Nassir Ghaemi, MD, MPH, Joseph Goldberg, MD
Time: 7:00 am - 5:00 pm
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