Continuing Professional Education, Courses (general) in the United States (USA)

Conference-Service.com offers, as part of our business activities, a directory of upcoming scientific and technical meetings. The calendar is published for the convenience of conference participants and we strive to support conference organisers who need to publish their upcoming events. Although great care is being taken to ensure the correctness of all entries, we cannot accept any liability that may arise from the presence, absence or incorrectness of any particular information on this website. Always check with the meeting organiser before making arrangements to participate in an event!

Meeting organisers can submit meetings free of charge for inclusion into the listing.

1.
 
WCS - CAPA — How to reduce, investigate, correct, and prevent Human Error in Manufacturing Processes
ID
797255
Dates
26 May 2016 - 27 May 2017
Location
Chicago, United States
Abstract
Course has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion . Human error is known to be the major cause of quality and production losses in many industries. Although it is unlikely that human error will ever be totally eliminated, many human performance problems can be prevented. Human errors start at the design stage. From procedures, training, and workplace environment many variables that affect human behavior CAN be manipulated reducing the likelihood of these occurrences. To work with these challenges it is really important to understand human behavior and the psychology of error as well as understand exactly where the systems weaknesses are, so they can be improved and/or fixed. This course offers practical approaches to address human performance issues in GMP related environments by using a specific methodology to investigate, correct, prevent and avoid re-occurrence of these issues.
Contact
World Compliance Seminars;     Phone: [844-267-7299];     Email: support@worldcomplianceseminars.com
2.
 
Seminar on the DHF, Technical File and Design Dossier - Similarities, Differences and the Future
ID
857623
Dates
02 Mar 2017 - 03 Mar 2017
Location
Las Vegas, NV, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
The Design History File, Device History Record, The Device Master Record, EU’s Medical Device Directive, Technical File Design Dossier, U.S. FDA’s DHF, FDA Compliance, FDA Regulations, Risk Analysis, Risk Management
3.
 
Seminar on HIPAA Security & Privacy Official - Roles and Responsibilities
ID
857688
Dates
02 Mar 2017 - 03 Mar 2017
Location
SFO, CA, United States
Abstract
Being the HIPAA Security and Privacy Official involves not only ensuring you know the appropriate patient rights and controls on your uses and disclosures of protected health information, but you also have the proper policies and procedures in place. If audited or the subject of a compliance review you will be required to show the government you have all the necessary documentation in place for safeguarding patient Protected Health Information and indicate how you addressed all required security safeguards. This starts with the fundamentals of a HIPAA compliance program.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
4.
 
Seminar on Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
ID
857632
Dates
02 Mar 2017 - 03 Mar 2017
Location
SFO, CA, United States
Abstract
This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
5.
 
Applied Statistics for Scientists and Engineers
ID
857631
Dates
02 Mar 2017 - 03 Mar 2017
Location
SFO, CA, United States
Abstract
Throughout 21 CFR and guidance documents for the pharmaceutical, biopharmaceutical, and medical device industries, the application of statistical methods are specified for: setting validation criteria and specifications, performing measurement systems analysis (MSA), conducting stability analysis, using design of experiment (DOE) for process development and validation, developing process control charts, and determining process capability indices. Different statistical methods are required for each of these particular applications. Data and tolerance intervals are common tools used for setting acceptance criteria and specifications. Simple linear regression and analysis-of-covariance (ANCOVA) are used for setting expiries and conducting stability analysis studies. Two-sample hypothesis tests, analysis-of-variance (ANOVA), regression, and ANCOVA are methods used for analyzing designed experiment for process development and validation studies. Descriptive statistics (distribution, summary statistics), run charts, and probability (distributions) are used for developing process control charts and developing process capability indices. This course provides instruction on how to apply the appropriate statistical approaches: descriptive statistics, data intervals, hypothesis testing, ANOVA, regression, ANCOVA, and model building. Once competence in each of these areas is established, industry-specific applications are presented for the participants.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
6.
 
Scientific Writing and Publication Techniques
ID
873859
Start date
09 Mar 2017
Location
Chicago, United States
Abstract
This is a one day course offering an extensive preparation for writing and publishing scientific manuscripts, with on-site exercises. I offer this one day course at Pittcon Expo in Chicago inside the short-course program. I also offer a two day course. Visit my website for more info and from there you can register by clicking on the Pittcon link.
Topics
manuscript writing, manuscript publication, research paper, research publications
7.
 
Applying ISO14971 and IEC62304 - A guide to practical Risk Management
ID
857707
Dates
09 Mar 2017 - 10 Mar 2017
Location
San Diego, California, United States
Abstract
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 regulatory compliant environment. This course will additionally address the software risk management and the resulting interfaces to device level risk management.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
8.
 
Effective Complaint Handling, Medical Device Reporting and Recalls
ID
857651
Dates
09 Mar 2017 - 10 Mar 2017
Location
San Diego, California, United States
Abstract
An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
9.
 
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods Los Angeles
ID
857727
Dates
09 Mar 2017 - 10 Mar 2017
Location
San Diego, California, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
10.
 
Requirements for Establishing an Effective Cleaning Validation Program
ID
857693
Dates
09 Mar 2017 - 10 Mar 2017
Location
San Diego, California, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
11.
 
Extracting information from geochemical data
ID
857692
Dates
09 Mar 2017 - 10 Mar 2017
Location
Houston, TX, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
12.
 
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods Los Angeles
ID
857746
Dates
16 Mar 2017 - 17 Mar 2017
Location
Seattle, WA, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
13.
 
Seminar on Leadership and Team Development for Managerial Success
ID
857767
Dates
16 Mar 2017 - 17 Mar 2017
Location
Chicago, IL, United States
Abstract
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.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
14.
 
Seminar on U.S. Payments Industry: The Players, Trends, and Compliance Issues Faced
ID
857766
Dates
16 Mar 2017 - 17 Mar 2017
Location
Chicago, IL, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
15.
 
Seminar on Validation, Verification and Transfer of Analytical Methods
ID
857809
Dates
20 Mar 2017 - 21 Mar 2017
Location
Zurich, Switzerland, United States
Abstract
Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should be verified to demonstrate the suitability of laboratories to successfully run the method and when methods are transferred between laboratories successful transfer should be demonstrated through testing. In case a laboratory wants to use an alternative method instead of a compendial method, equivalency of the alternative method to the compendial method should be demonstrated.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
16.
 
BTOES 17 — Business Transformation & Operational Excellence World Summit
ID
820494
Dates
21 Mar 2017 - 24 Mar 2017
Location
Orlando, FL, United States
Abstract
This event represents the largest gathering of industry leaders, innovative disruptors, and leadership-level thought leaders across the entire business transformation, innovation execution & operational excellence ecosystem. It has been uniquely designed, to drive the best attendees, deliver exceptional content, and become the most engaging event in the industry. Find out more at http://bit.ly/200h46q
Contact
Charlotte Kelly;     Email: charlotte.kelly@proqis.com
Topics
operations, excellence, process, business, transformation, summit, awards, industry, opex, pexweek, technology, innovation, strategy, development, ecosystem, lean, six, sigma, training, agility, leadership, tech, software, healthcare, bpm, start up
Event website
17.
 
Seminar on HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties
ID
857819
Dates
23 Mar 2017 - 24 Mar 2017
Location
Washington, DC, United States
Abstract
This session is designed to provide intensive, two-day training in HIPAA compliance, including what's new in the regulations, what's changed recently, and what needs to be addressed for compliance by covered entities and business associates.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
18.
 
Seminar on HR Auditing: Identifying and Managing Key Risks
ID
857730
Dates
23 Mar 2017 - 24 Mar 2017
Location
Washington, DC, United States
Abstract
R audits are designed to help your organization focus its attention on its human resource management practices, policies, procedures, processes, and outcomes by providing you with a structured and systematic series of questions about key compliance, risk management, internal auditing, and human resource management issues. As a process, HR audits are designed to help your organization identify potential and actual problem areas, help assess the effectiveness of current HR management activities, help assess weaknesses in HR internal control processes, and help assess human capital strategic and compliance related risks. HR audits should additionally provide suggestions for corrective action.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
19.
 
HIPAA Survival - All you need to Know
ID
857784
Dates
23 Mar 2017 - 24 Mar 2017
Location
San Diego, California, United States
Abstract
This seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audits occur. It will also address major changes under the Omnibus Rule and any other applicable updates for 2017. Areas covered will be texting, email, encryption, medical messaging, voice data and risk factors as they relate to IT.
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
20.
 
Supplier Management for Medical Device Manufacturers
ID
857827
Dates
23 Mar 2017 - 24 Mar 2017
Location
Washington, DC, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
21.
 
Compliance Boot Camp
ID
857848
Dates
23 Mar 2017 - 24 Mar 2017
Location
Washington, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
22.
 
Medical CBT for Depression: Ten-Minute Techniques for Real Doctors (Maui, 2017)
ID
808525
Dates
27 Mar 2017 - 29 Mar 2017
Location
Maui, United States
Abstract
Aloha! CBT Maui will be held at the spectacular Sheraton Maui on the world-class Kāʻanapali Beach from March 27-29, 2017. Workshop hours are 8:00AM to 12:15PM on the Monday, Tuesday & Wednesday, leaving you free all other times to explore the beautiful island of Maui. The workshop is the acclaimed CBT for Depression module, accredited for 12.0 Mainpro-Cs by the College of Family Physicians of Canada. Please join us and you'll gain a plethora of ultra-brief techniques to help your patients defeat depression and be happy. General interest topics covered include procrastination, perfectionism, rumination, self-criticism, self-handicapping, letting go of the past, decision-making, and evidence-based marital enrichment. Head instructor Greg Dubord, MD is nicely warmed up after giving over 300 CBT workshops, and is a recent University of Toronto CME Teacher of the Year. Seasoned assistant faculty includes Peter Duffy, MD, CCFP(EM), CMCBT, Co-Director of the Certificate in Medical CBT program.
Contact
CBT Canada;     Phone: [8774668228];     Email: info@cbt.ca
Topics
cognitive behavior therapy (cbt), depression, procrastination, perfectionism, rumination, self-criticism, self-handicapping, letting go of the past, decision-making, evidence-based marital enrichment
Related subject(s)
23.
 
Design of Experiments (DOE) for Process Development and Validation
ID
857814
Dates
30 Mar 2017 - 31 Mar 2017
Location
Los Angeles, CA, United States
Contact
Event Manager;     Phone: [(800) 447-9407];     Email: support@globalcompliancepanel.com
Topics
FDA Compliance Training
24.
 
Medical CBT Tools: Ten-Minute Techniques for Real Doctors (Kauai, 2017)
ID
808548
Dates
10 Apr 2017 - 12 Apr 2017
Location
Kauai, United States
Abstract
Aloha! CBT Kauai will be held at the truly spectacular Grand Hyatt on sunny Poipu Beach from April 10-12, 2017. The workshop is only four hours per day on the Monday, Tuesday & Wednesday, leaving you free all other times to explore the exuberant Garden Island. The CME is the foundational CBT Tools module (12.0 Mainpro-Cs). Join us on Kauai and you'll learn a multitude of ultra-brief CBT techniques to make your work much easier with both medical and psychiatric patients. Head instructor Greg Dubord, MD is a recent University of Toronto CME Teacher of the Year and is nicely warmed up after giving over 300 CBT workshops. Seasoned assistant faculty includes Peter Duffy, MD, CCFP(EM)(LM), CMCBT, Co-Director of the Certificate in Medical CBT program.
Contact
CBT Canada;     Phone: [8774668228];     Email: info@cbt.ca
Related subject(s)
25.
 
FASEB SRC — Mobile DNA in Mammalian Genomes
ID
877099
Dates
18 Jun 2017 - 23 Jun 2017
Location
Big Sky, Montana, United States
Abstract
This SRC is focused on the dynamic nature of mobile DNAs in mammalian genomes and their phenotypic impacts. Topics will encompass mechanistic and evolutionary aspects of diverse types of retrotransposons, including LINE-1 and endogenous retroviruses, as well as DNA transposons and related human genes. Attendees will also explore interactions between these sequences and the epigenome and endogenous machinery of DNA repair and rearrangement. These elements comprise are a major portion of our DNA, and are significant contributors to genomic diversity in the form of structural variation. While the germ line is a well-known site of activity of mobile genetic elements, there is increasing evidence for expression and mobility in somatic cells and in human diseases, particularly cancers. This makes it an exciting time for the field. Moreover, new insights are being gained into roles of mobile elements in shaping gene regulatory networks in normal cells. Finally, harnessing mobile genetics elements as tools for forward genetic screens or gene delivery has provided new capabilities to change the genome. This is a long standing meeting, certain to be thought provoking, animated, and collegial all at once.
Contact
FASEB SRC Staff;     Phone: [3016347010];     Email: src@faseb.org
Topics
Structural biology, bioinformatics, genome engineering

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Last updated: 11 February 2017