GlobalCompliance March Seminars 2016

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GlobalCompliancePanel March Seminars 2016

• GlobalCompliancePanel is a training source that
  delivers diverse, high quality regulatory
  compliance trainings. GlobalCompliancePanel
  imparts knowledge of best practices across a
  broad range of user-friendly mediums such as
  webinars, seminars, conferences and tailored,
  individualized consulting. 
• More Information Click here
• http//www.globalcompliancepanel.com/seminar

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GlobalCompliancePanel Seminars Categories

• Fda Compliance
• Clinical Compliance
• Drugs and Biologics
• Medical and surgical
• Food
• SOX Compliance
• IT control and PCI
• Biotechnology
• Laboratory Compliance
• Packing and Labeling
• Quality and ISO 9000 Compliance
• Risk management
• HR Compliance

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Supplier Management for Medical Device
Manufacturers

• In this seminar you will review all the quality
  management system requirements of FDA and ISO
  13485 and then learn how to set up and manage an
  audit system that complies with these
  requirements, yet is risk-based so that your
  company makes the most efficient use of auditing
  resources for both internal and supplier audits.
  The seminar will include interactive exercises to
  reinforce the fundamentals of conducting and
  documenting quality system audits. Auditing
  principles taught in this seminar will be based
  on ISO 190112011 Guidelines for auditing
  management systems.

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• Date March 3rd 4th, 2016Time 900 AM to
  600 PMLocation Berlin, GermanyVenue WILL BE
  ANNOUNCED SOONDirector Betty Lane
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900418SEMINAR

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New HIPAA Audit Enforcement Activities Being
Prepared to Show your Compliance

• The evolutions of this enigmatic law and how what
  was once relative benign in terms of enforcement
  is now fully funded and aggressive. Learn what
  you can do to be prepared for an audit and how to
  lower risks of ever being audited.
• It is absolutely imperative that you are
  proactive and not reactive with your compliance
  program, this is a necessary evil and you need to
  protect your practice or your business and limit
  risks from the imminent Federal audits. Join me
  in keeping up with this very confusing law and
  take advantage of all the templates and
  information provided as part of the seminar.

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• Date March 3rd 4th, 2016Time 900 AM to
  600 PMLocation Washington, D.C
• Venue Courtyard Arlington Crystal City/Reagan
  National Airport
• Address 2899 Jefferson Davis Highway Arlington,
  VA 22202 USA
• Director Brian L Tuttle
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900346SEMINAR

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Fundamentals of Statistical Process Control

• This 2-day seminar provides the information you
  need to use one of the most powerful tools in
  quality, statistical process control. It will
  help people in design, quality, and production
  understand the concepts and effectively implement
  them. The examples and issues in the seminar come
  primarily from the medical device industry, but
  the material is applicable to any production
  environment.
• This seminar provides a practical approach to
  understanding and implementing SPC. It provides
  the tools you need, presents an explanation of
  how to use them, and offers practice through
  exercises.

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• Date March 3rd 4th, 2016Time 900 AM to
  600 PMLocation Washington, D.C
• Venue Courtyard Arlington Crystal City/Reagan
  National Airport
• Address 2899 Jefferson Davis Highway Arlington,
  VA 22202 USA
• Director Dan O'Leary
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900369SEMINAR

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Presentation Skills for Technical Professionals

• Presentation Skills for Technical Professionals
  is a hands-on workshop that helps participants
  become comfortable, confident, and masterful
  presenters. The principles presented will be
  applicable to all business settings. Course
  content will be customized to focus on the
  interests and concerns of all attending.
• Participants will be given practice exercises
  designed specifically for them. They will have
  the opportunity to make several presentations and
  receive positive feedback and personal coaching
  from the instructor.

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• Date March 3rd 4th, 2016Time 900 AM to
  600 PMLocation Washington, D.C
• Venue Courtyard Arlington Crystal City/Reagan
  National Airport
• Address 2899 Jefferson Davis Highway Arlington,
  VA 22202 USA
• Director Robert Elliott
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900431SEMINAR

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Maritime Safety Course 7615 for Shipyard
Employment

• The growth in the Outreach Training Program from
  OSHA is a result of industry-wide acceptance and
  additional training opportunities available
  through OSHAs Training Institute (OTI) Education
  Centers. Many employers use the OSHA Outreach
  Training Program to provide training for their
  employees.
• This training program provides basic safety and
  health information and education. The OSHA
  Outreach Training Program for the Maritime
  Industry provides training for workers and
  employers on the recognition, avoidance,
  abatement, and prevention of safety and health
  hazards in workplaces in the maritime industry,
  specifically shipbuilding, shipbreaking and ship
  repair. The U.S. Navy requires this training for
  all contractors who work aboard a ship, whether
  in dry dock or under way, including consultants.

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• Date March 3rd 4th, 2016Time 900 AM to
  600 PMLocation Washington, D.C
• Venue Courtyard Arlington Crystal City/Reagan
  National Airport
• Address 2899 Jefferson Davis Highway Arlington,
  VA 22202 USA
• Director Chuck Northam
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900385SEMINAR

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Safety, Health Environment Management System
through Standards Practices

• A management system, by definition, is a process
  by which a function or functions are carried out
  in an organization by a series of hierarchal
  documents that are prescriptive, and set a
  particular path on which the organization manages
  its day-to-day operations.
• The SHE, plus training and security are the
  functions we will build the standards and
  practices around. There are 16 functions that
  cover the SHE TS world. We build a standard and
  practice around all 16 functions. Supporting
  documents, associated programs, procedures or
  standard operating procedures (SOP) will be a
  part of the particular function being managed. 

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• The standards and practices that are put in place
  act as the cornerstone for decisions being made
  relative to resources and dollars spent within
  the SHE scope of business.
• This process accomplishes the following
• Identifies the things that need to be managed
  within the function
• Construct a process, tool, or mechanism that best
  manages each of those things identified
• They are usually a set of standards, practices
  and programs that are built specifically for a
  particular function
• Build the standard, practice or program so that
  it can be adjusted according to results
• Build a measuring metric, benchmark or scorecard
  with both lagging and leading indicators
• Build the management system in a way that is
  hierarchal in structure within the organization -
  (corporate sets and standards and the business
  unit builds the practice around the standard)

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• Date March 10th 11th, 2016Time 900 AM to
  600 PMLocation Chicago, IL
• Venue Four Points by Sheraton Chicago O'Hare
• Address 10249 West Irving Park Road, Schiller
  Park, IL 60176, USA
• Director James J. Thatcher
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900387SEMINAR

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Clinical Research for Cardiovascular
Pharmaceuticals Ensuring Compliance of
Traditional and New Cardiovascular Medications

• This seminar should be attended to ensure the
  proper compliance and development of traditional
  and new cardiovascular medications. Failure to
  attend could result in poorly managed clinical
  trials, wasted financial resources and liability
  based law suits. The development of well-designed
  clinical trials and rigorous monitoring is
  required. From the literature review to the last
  appendix a complete understanding of regulations
  pertaining to clinical research and monitoring a
  well-designed protocol is necessary. All project
  managers know that the critical path thru
  clinical research is extremely tightly regulated
  and fraught with pitfalls.

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation San Diego, CA
• Venue Four Points By Sheraton San Diego Downtown
• Address 1617 1st Avenue - San Diego,
  California, 92101 - United States
• Director Charlene M. JettClick Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900400SEMINAR

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Supplier Management for Medical Device
Manufacturers

• This course is designed for people who preform or
  manage audits of a medical device quality
  management system, including internal and or
  supplier audits. Both 21 CFR 820 Quality Systems
  Regulation (cGMP) and ISO13485 and Quality
  Management Systems auditing will be covered.
• This course will be particularly helpful to the
  following Senior quality managers who need to
  establish or manage an audit program
• Quality professionals who need to know how to
  conduct effective internal or supplier audits
• Regulatory professionals responsible for
  compliance
• Internal or supplier auditors who need a better
  understanding of the auditing processor medical
  device quality management system requirements
• New internal or supplier auditors
• Audit Managers who need to update or streamline
  your internal auditing process
• All Managers who need to establish an internal or
  supplier audit program

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation San Diego, CA
• Venue WILL BE ANNOUNCED SOON
• Director Betty Lane
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900448SEMINAR

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Tools and Techniques for Operational Risk
Management Regulatory Aspects

• In this seminar, we go through the known
  techniques of operational risk management,
  including of course the regulatory aspects, and
  point to a few shortcomings that appeared in
  several (possibly nameless) banks.
• We then go on to highlights on the pitfalls that
  await risk managers on the next Frontier, from
  which what activities to outsource, setting up a
  risk appetite, developing a risk culture and a
  commensurate set of governance processes, what to
  ensure and not, separating or breaking the silos
  of risk.
• We suggest the extended use of a risk management
  framework proper to operational risk,
  implementable in most institutions, regardless of
  complexity of operations.
• We highlight extreme risks, for which Basel III
  was strangely mute, but which are highly relevant
  to the 2008 crisis. We suggest some pitfalls to
  avoid.
• During this highly interactive seminar, group
  exercises will be performed, as well as case
  studies including role games.

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation Chicago, IL
• Venue Four Points by Sheraton Chicago O'Hare
• Address 10249 West Irving Park Road, Schiller
  Park, IL 60176,USA
• Director Fred Vacelet
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900394SEMINAR

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Analytical Instrument Qualification and
Validation Understanding to Prepare for FDA
Audits to become Part 11 Compliant

• In this two day workshop conference you will
  learn the different global agencies expectations
  of analytical equipment qualification along with
  the development of a sound process validation
  program in order to develop and implement
  bulletproof solutions that are accepted,
  effective, and efficient. Through case study
  analysis we will examine best practices to
  provide thoughts and ideas to develop or improve
  the performance of your current system.
  Additionally, case studies will explore how your
  management practices of your analytical equipment
  qualification/ validation and process validation
  programs can help or hurt your legal liability
  and the legal issues that arise from
  nonconformance with regulators and Auditors.
• This seminar will help attendees understand the
  instrument qualification and system validation
  processes and will provide instruction on how to
  prepare for FDA audits and how to become part 11
  compliant.

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation SFO , CA
• Venue WILL BE ANNOUNCED SOON
• Director Joy McElroy
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900454SEMINAR

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Risk Analysis and Design of Experiments in
Process Validation and Development

• This course is designed to help scientists and
  engineers plan and conduct experiments and
  analyze the data to develop predictive models
  used to optimize processes and products and solve
  complex problems. DOE is an extremely efficient
  method to understand which variables (and
  interactions) affect key outcomes and allows the
  development of mathematical models used to
  optimize process and product performance. The
  models also provide an understanding of the
  impact of variability in controllable and
  uncontrollable factors on important responses.
  The concepts behind DOE are covered along with
  some effective types of screening experiments.
  Case studies will also be presented to illustrate
  the use of the methods.

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation San Diego, CA
• Venue Four Points By Sheraton San Diego Downtown
• Address 1617 1st Avenue - San Diego,
  California, 92101 - United States
• Director Steven Wachs
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900404SEMINAR

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Leadership and Team Development for Managerial
Success

• Inspire and influence your team members to
  achieve your goals as a team!
• Managers who will be promoted are the ones who
  not only manage efficiently but also lead their
  teams effectively. Learn how to work in a
  horizontal mode of operation.. apply a consistent
  theory in leading your team.. and teach critical
  leadership skills to members of your team, so
  each and every one of them can lead the team in
  your absence.

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• Date March 10th 11th, 2016
• Time 830 AM to 530 PMLocation Chicago, IL
• Venue Four Points by Sheraton Chicago O'Hare
• Address 10249 West Irving Park Road, Schiller
  Park, IL 60176, USA
• Director Chris DeVany
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900411SEMINAR

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Process Validation Guidance Requirements (FDA and
EU Annex 15 Qualification and Validation)

• This two day Seminar provides a conduit to
  enhance your understanding of the utilization of
  Process Validation and Phase 1, 2 and 3, where
  their Guidance blend and where they remain
  distinct. In particular, Stage 3 Continued
  Process Verification, will be reviewed in detail.
  Where does it begin what is included and, when
  does it end.
• The Process Validation Guidance for Industry was
  recently revised after many years. With the
  emphasis today on being able to assure that a
  process is meeting its requirements through
  Validation, and not simply through Verification
  or Qualification, an understanding of both its
  importance and how to accomplish this feat has
  come to the fore. In addition, with ICH Q9, Risk
  Management, involved in every aspect of our day
  to day operations, it becomes especially
  important to learn how this meshes with Process
  Validation. The FDA and especially CDER, with
  their new auditing format, will be wanting to
  understand how each Company performed their
  Validations in all areas to include manufacturing
  and Quality. Having an enhanced understanding of
  the Process Validation Guidance will assure that
  your firm is meeting the FDA?s current
  requirements.

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• Date March 10th 11th, 2016
• Time 900 AM to 600 PMLocation San Diego, CA
• Venue WILL BE ANNOUNCED SOON
• Director Barry A Friedman
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900450SEMINAR

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Beyond HIPAA Patient Medical Records and Client
Confidentiality in Mental Health

• This program offers an objective, thorough review
  of client confidentiality for mental health
  practitioners beyond HIPAA, including state laws
  governing confidentiality, state evidentiary
  rules, and mandated exceptions under duty to warn
  and other laws.
• Because each state and each mental health
  profession has its own rules, duties, and
  obligations on client confidentiality apart from
  record keeping requirements, it is crucial to
  know the sources of these laws and how they
  apply.
• This seminar will first review the standardized
  HIPAA requirements for patient medical records.
  From that perspective, the seminar will answer
  the issues presented by expanding to review state
  laws on patient confidentiality, evidentiary
  privileges, and exceptions mandated by law.

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• Date March 17th 18th, 2016
• Time 900 AM to 500 PMLocation Atlantic
  city, NJ
• Venue Trump Taj Mahal
• Address 1000 Virginia Avenue, Atlantic City, NJ
  08401, United States
• Director Mark Brengelman
• Click Here
• http//www.globalcompliancepanel.com/control/globa
  lseminars/product_id900323SEMINAR

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