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
797222
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.
 
ORBMC — OR Business Management Conference
ID
823894
Dates
30 Jan 2017 - 02 Feb 2017
Location
New Orleans, United States
Abstract
In today's healthcare environment, meeting budget requirements, improving efficiencies and patient throughput, and making the best use of technology are among the daily challenges across facilities nationwide. As regulations and recommended practices change, reimbursements are reduced, and Medicare penalties rise, continuing education becomes increasingly important. The OR Business Management Conference is the premier educational opportunity for operating room business managers, directors, and other perioperative services professionals to learn about the latest best practices from leading industry experts from across the nation while enjoying the energetic and colorful city of New Orleans.
Contact
Email: mhanoon@accessintel.com
Topics
operating room management, operating room business, OR business management
Related subject(s)
3.
 
PRIMO — 2017 Practical Considerations in Immuno and Molecular Oncology (PRIMO) Annual Meeting
ID
807175
Dates
09 Feb 2017 - 12 Feb 2017
Location
Maui, United States
Abstract
The Practical Considerations in Immuno and Molecular Oncology (PRIMO) Meeting is an annual CME-certified conference to help practicing providers keep up with the latest advances in immuno and molecular targeted therapies. This year’s meeting is scheduled to take place February 9-12, 2017 in Wailea Beach, Maui, Hawaii and will help providers address real world issues on how and when to optimally integrate these new therapies into their clinical practice, and also provide insight into new advances in immune and molecular targeted therapies that are expected to report new data in 2017.The PRIMO Meeting is for those who want a streamlined review of the most recent advances in immuno and molecular oncology delivered by some of the top experts in their respective field. This meeting is for practicing oncologists, hematologists, research fellows, and nurses. Interested parties can log on to www.primomeeting.org for more information.
Contact
Jen Mahon;     Phone: [1-855-677-4668];     Email: info@primomeeting.org
Topics
oncology, continuing medical education, immunotherapy
Related subject(s)
4.
 
ACT BootCamp - San Diego
ID
854714
Dates
16 Feb 2017 - 19 Feb 2017
Location
San Diego, United States
Abstract
For the last few years, if you mention you’re interested in Acceptance and Commitment Therapy (ACT), the next question you’re likely to hear is, “Have you been to BootCamp?” This essential workshop has been the foundation of ACT training for thousands of practitioners like you. Whether you’re hearing about ACT for the first time or already have formal training, this workshop can take your skills to the next level.
Contact
Courtney Kendler;     Email: events@praxiscet.com
Topics
ACT, acceptance and commitment therapy, CBT, Behavior Analysis, DBT, Psychodynamic therapy, psychology, social work, MFT, counseling BCBA
Related subject(s)
5.
 
Seminar on the DHF, Technical File and Design Dossier - Similarities, Differences and the Future
ID
857645
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
6.
 
Seminar on HIPAA Security & Privacy Official - Roles and Responsibilities
ID
857666
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
7.
 
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
8.
 
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
9.
 
Applying ISO14971 and IEC62304 - A guide to practical Risk Management
ID
857685
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
10.
 
Effective Complaint Handling, Medical Device Reporting and Recalls
ID
857695
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
11.
 
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods Los Angeles
ID
857716
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
12.
 
Requirements for Establishing an Effective Cleaning Validation Program
ID
857704
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
13.
 
Extracting information from geochemical data
ID
857714
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
14.
 
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods Los Angeles
ID
857713
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
15.
 
Seminar on Leadership and Team Development for Managerial Success
ID
857756
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
16.
 
Seminar on U.S. Payments Industry: The Players, Trends, and Compliance Issues Faced
ID
857744
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
17.
 
Seminar on Validation, Verification and Transfer of Analytical Methods
ID
857798
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
18.
 
BTOES 17 — Business Transformation & Operational Excellence World Summit
ID
820461
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
19.
 
Seminar on HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties
ID
857753
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
20.
 
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
21.
 
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
22.
 
Supplier Management for Medical Device Manufacturers
ID
857783
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
23.
 
Compliance Boot Camp
ID
857804
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
24.
 
Medical CBT for Depression: Ten-Minute Techniques for Real Doctors (Maui, 2017)
ID
808492
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)
25.
 
Design of Experiments (DOE) for Process Development and Validation
ID
857770
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
26.
 
Medical CBT Tools: Ten-Minute Techniques for Real Doctors (Kauai, 2017)
ID
808559
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)

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Last updated: 14 December 2016