Recently Added Seminars and Training Programs

Training Seminars and Classes
From Compliance Trainings
Pharmaceutical Compressed Air Quality GMP Standards and Requirements A detailed description of a typical pharmaceutical compressed air system with its individual components is provided. Engineering schematics are included. All component functions are detailed with recommendations as to which component type is considered optimal. The four contamination sources in compressed air are discussed. These are: a) solid particulate b) water content c) total oil content d) microbial bioburden For each of these, the presentation will discuss cause and effect. Suggestions are also provided for prevention of the contamination. Finally, a compilation of all FDA/ EU GMP Guidances, USP/ EP and ISO air standards are presented. Sampling and testing methodology for each of these specifications is discussed.  more...
Writing Effective Standard Operating Procedure SOPs and Work Instructions WIs Writing effective Standard Operating Procedures and Work Instructions is not intuitive, it is not a skill that is often taught in our universities, and it can be a difficult and cumbersome task to execute. Knowing the most effective and efficient processes for gathering, organizing, and writing technical documentation is absolutely critical to providing significant value to a dreaded, avoided, and seemingly unimportant work task. This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.  more...
Solving Statistical Mysteries What does the FDA want This webinar provides an overview of what it appears the FDA is looking for in the use statistics by taking illustrative examples from warning letters and industry experiences and approaches that have worked in a variety of situations. Use of statistics has been part of the FDAa ™s guidance and regulations for many years. Use of statistical tools is an integral part of the Jan 2011 FDA Process Validation Guidance. It can be argued that the FDA is looking for the pharma and biotech industries to make even greater use of statistical thinking and methods. Even with this long history, the use of statistics seems to be a source of uncertainty and anxiety for many.  more...
Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation This session by our expert speaker, Dr. David Lim, is further intended to increase our awareness that an adequate implementation and management of part 11 and computer system validation can greatly increase patient safety by reducing the likelihood of compromising data quality and integrity including computer system validation. FDA frequently states a failure to maintain complete data; failure to prevent unauthorized access or changes to data and to provide adequate controls to prevent omission of data; a failure to validate computer software for its intended use according to an established protocol when computers or automated data processing systems are used as part of production or the quality systema .a  more...
HIPAA How to Put a Compliance Program in Place Being in compliance with HIPAA involves not only ensuring you provide 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.  more...
From Compliance4all
Guidelines for New FDA Transfer of Analytical Methods - 2017 Overview: When validated methods are transferred between laboratories and sites, their validated state should be maintained to ensure the same reliable results in the receiving laboratory. For a long time there was no official guidance on what exactly is expected to maintain 'the validated state'.  more...
Medical Device Employee Training - 2017 Overview: This is especially true for start-up and other small medical device companies, or rapidly growing companies. Specific FDA training requirements will be presented.  more...
Phase I GMPs clinical trials - 2017 Overview: Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lower doses of the drug product.  more...
FDA Scrutiny of Promotion and Advertising - 2017 Overview: DTC may be deemed as misbranding your product and, therefore, may not be marketed. Firms must be more sophisticated now in designing their advertising methods and messages. The days of looking at text alone for a magazine insert are long gone.  more...
How FDA Trains its Investigators to Review CAPA - 2017 Overview: In this session will be a section-by-section summary of the CAPA subsection of the QSIT, the document by which FDA inspectors operate during an inspection, as well as how your company can use that same document to increase the likelihood of a positive outcome during the inspection.  more...
Implementing a Technology Transfer Process - 2017 Overview: It will cover the concepts associated with transferring the scientific technology needed to manufacture the product, processes to ensure the receiving manufacturing facility is ready for the product and tools and templates to help capture the knowledge.  more...
Excel Spreadsheets - Step-By-Step Instructions - 2017 Overview: This interactive webinar provides explicit details and live demonstration followed by a collaborative workshop that explains how to configure and validate a GxP compliant spreadsheet application.  more...
Understanding International ACH - 2017 Overview: Instructor will cover customer benefits and value proposition regarding International ACH and why it may be preferred over wire transfers.  more...
Tools for Human Error Reduction - 2017 Overview: 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.  more...
FDA current recommendations on using electronic health records - 2017 Overview: This webinar will discuss FDA's current recommendations on using electronic health records in prospective clinical investigations of human drugs, biologics, medical devices and combination product.  more...
Good Deviation Practice - CAPA Process - 2017 Overview: This course explores the deviation and CAPA processes and best practices for both. It shows how to avoid pitfalls and minimize regulatory scrutiny by having a robust deviation/ CAPA system and thorough investigations.  more...
Review process on Advertising Promotional material compliance - 2017 Overview: You will hear about the opportunities for input from regulatory agencies at critical stages and on key promotional materials and you will hear strategies for implementing review process and procedures to facilitate high compliance standards.  more...
How to Meet FDA QSR and ISO 13485 Requirements - 2017 Overview: A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures.  more...
From Compliance Trainings
FDAs 21 CFR Part 11 Add-on Inspections In this webinar, our presenter John Lincoln, will address the use of the FDA guidance documents, GAMP, 21 CFR 11, and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Risk Management models, and their real-world implementation. This session will also discuss and explain about a compliant, field tested (FDA and Notified Body) 21 CFR Part 11 software documentation model.  more...
FDA Quality System Inspection Technique QSIT Audits Good Preparation Practices This webinar presents important facts to simplify the planning and execution to ensure that the findings by FDA as 483s or as the more serious warning letters are addressed appropriately so your quality system is always audit proof and ready for the QSIT Inspectors. After having successfully emerged out of a FDA 483 or a warning letter for your medical devices, it is a challenge to maintain the items that you promised to a correcta in your response letter to the FDA as the FDA auditors will dig deep into those items. Hence items that can be scrutinized under a mock QSIT audit by experienced auditors / consultants to confirm your readiness for an unannounced FDA audit will be covered. How to perform a risk-based mock QSIT assessment for your medical device quality system for the key  more...
FDAs Two New Draft Guidance on Software and Device Changes and the 510k This is a long awaited clarification of U. S. FDAa ™s Memo K97-1 for medical device manufacturers, with far-reaching effects in regulatory compliance regarding device changes and 510(k) a re-submissionsa , as envisioned by the FDA. A must-know for all pharmaceutical and medical device industry professionals and organizations. This session help you implement formal methods with documented and defensible rationalea which will prepare your organization for further 510(k) changes in the future, especially if your company is in the Medical Device and combination products fields.  more...
FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies This webinar will: Provide attendees a better understanding of the current audit techniques used by the FDA and how they have changed over the years Analysis of the top 10 most cited GMP drug manufacturing deficiencies over the last year Review of the significant increase in the number of warning letters issued over the last four years Review common areas of focus during audits Provide a template that companies can use to evaluate their own state of compliance Demonstrate examples to highlight various points discussed  more...
From ZaranTech.com
Live Webinar about SAP UI5 and FIORI Hi All, You are most welcome to join our Upcoming Free Webinar for #SAP UI5 and FIORI. Details of the same is as follows: Demo #Webinar: 23rd March, 2017 @ 7: 30 pm CST REGISTER for Live Demo: More info Contact us: info@zarantech. com (or) +1-515-309-7846 About the Course SAP Fiori is a group of applications that has been written recently by SAP to address often used SAP functions like self-service tasks, workflow approvals, and information lookups. SAP Fiori provides simple access across smartphones, desktops, and tablets. It is an impressive initiative from SAP to provide a quicker and highly responsive user interface. It employs cutting-edge design principles for delivering simple and responsive experiences which are personalized and across different devices from  more...
Live Webinar about SAP S4HANA Simple Logistics on-line e-learning cbt (computer based) Hi All, You are most welcome to join our Upcoming Free Webinar for #SAP S4HANA Simple Logistics. Details of the same is as follows: Demo #Webinar: 23rd March, 2017 @ 8: 00 pm CST REGISTER for Live Demo: More info Contact us: info@zarantech. com (or) +1-515-309-7846 About the Course: SAP Simple Logistics is a one stop solution for new-age Material Management, Production Planning, Supply Chain Management, as well as sales and distribution of organizations with medium to large infrastructure. SAP Simple Logistics is also known as SAP S4HANA Enterprise Management which includes all the modules not only the Finance but also the modules like SAP MM, SAP SD and now they are available as a part of SAP S4HANA as a product and enterprise management is the complete business street.  more...
From PsyAsia International
Online Training - Psychometric Assessment at Work Course - BPS Level 1 2 PsyAsia International, Asiaa ™s independent leader in Psychometric Test Training is now offering an online training in Psychometric Assessment at Work Course - BPS Level 1 & 2. This training course focuses on Psychometric Testing for the Workplace and hence very relevant to Human Resources and allied professionals. Learners will be taught how to evaluate and therefore choose psychometric tests, how to administer, score and interpret them, and how to use psychometric tests in the decision-making process. Supported Intake Mode: Course Dates: 12th of June to 30th of October, 2017 After successful completion of the course, you will be qualified to order, administer, score, interpret and feedback on a complete range of ability and aptitude tests as well as multiple personality  more...
Behavior-Based Interviewing Course Singapore The interview is a common tool for employee selection. However, many interviewers have never been formally trained and it has long been recognized that there is little intra- and inter-rater reliability (consistency) where traditional non-structured interviews are utilized. This one or two day Behavior-based Interviewing Course provides busy recruitment agency staff, human resource managers/ professionals, selection panels and line management with effective tools for increasing the objectivity and standardization of interviews. Training focuses on the objective and structured interview technique with the greatest support for scientific validity: the Behavior-based Interview, also referred to as the Competency-based Interview. Behavior Based Interviewing Course Details: Date: 18th of  more...
From MentorHealth
Webinar on 2017 Principles of IRB Review This webinar will discuss how IRBs can review research to fulfill the regulatory requirements as well as conduct appropriate and complete ethical review of research protocols. Many examples will be provided distinguishing between what must be done to fulfill the regulatory requirements and what should be done for ethical review.  more...
Webinar on HIPAA Enforcement Activity Now that the HIPAA rules have been in place for more than a dozen years, the days of advice and counseling have been replaced by a hard-nosed enforcement attitude, where HHS OCR is ready to make health care organizations that violate the rules feel some pain for their actions.  more...
Webinar on CMS CERT Comprehensive Error Rate Testing CMS oversees the CERT program. The objective of the CERT program is to estimate the accuracy of the Medicare FFS program by conducting improper payment measurements. Our discussion will provide the following: 1. Summary of the CERT program and how it affects healthcare providers 2. Improper payment measurement history 3. CERT process and how to respond 4. Prevention Strategies  more...
Webinar on Recognizing and Responding to Personality Disorders in College Students What exactly is BPD? Trying to explain it to someone who has never experienced it can be quite a daunting task. My psychiatrist describes borderline personality disorder as having an "emotional sunburn." Imagine touching the skin of a person without a sunburn as opposed to touching the skin of someone with a horrible, blistering burn. While the person without a sunburn will be fine, the one with a sunburn will be in excruciating pain  more...
Webinar on HIPAA Audits I will be speaking to real life audits conducted by the Federal government for Phase 2 and beyond (Ia ™ve been on both sides of these audits) what your highest risks are for being fined (some of the risk factors may surprise you).  more...
World Economies Cosmetic Regulations Webinar During the webinar Participants will be addresses on the key regulatory provisions for cosmetic products in the major global economies. The EU's new Cosmetic Product Regulation (EU CPR) will be given a certain, wider position as the EU CPR is representing the latest, most modern regulatory framework which is influencing other global legislators.  more...
Webinar on MACRA Countdown Training Options Duration: 60 Minutes Wednesday, May 3, 2017 | 10: 00 AM PDT | 01: 00 PM EDT Overview: In this session Mr. Wolfe will provide an overview of the Quality Payment Program, including its MIPS and Advanced APM pathways. Mr. Wolfe will provide a straight-forward, practical explanation of key provisions and options for clinicians and health care leaders as they navigate the 2017 transition year and beyond. Why should you Attend: Going forward, clinicians and health care leaders need to be developing strategies so they can position their organizations for financial success under the new Quality Payment Program. Beginning in 2017, CMS will start rewarding clinicians for their delivery of high-quality patient care through one of two pathways: 1. Payment of incentives for  more...
From NOON Infotech
IBM WebSphere Commerce Server Development Batch starting this Week IBM Commerce Server Development Training by an Experienced professional. It will be a Real-time Hands-on Training with *Excellent Training material Provided(Study, Interview & Certification) *Software for Practice(VM Ware Version) Contact for Demo Session & other details. Share with your friend whoever may be interested.  more...
PEGA CLSA 71 Certification Part 1 and Part 2 Support instructor led trainingon-line e-learning cbt (computer based)courseware PEGA Online Training by Industry Experts having hands on experience. PEGA 7. 1 CSA, CSSA, CLSA PEGA Online Batches Starting It will be Real-time Hands-on Training. Training by Developing a project Throughout the training. Imparting Practical understanding of the PEGA tool. Excellent Training material Provided(Study, Interview & Certification) Contact immediately to block your seat  more...
SAS Base and Advance online and classroom training instructor led trainingon-line e-learning cbt (computer based)courseware Greetings from NOON Infotech We have excellent trainers for SAS Base & Advance having more than 7 years of industry experience & great exposure to real-time issues, also give the training, they are working in senior positions in MNC`s. We have successfully completed SAS Training for more than 15 batches In India & USA. We are starting a new batch on every alternate week. It will be a Real-time Hands-on Training. Training by Real time Scenarios. Imparting Practical understanding of the SAS tool. Excellent Training material Provided(Study, Interview & Certification) Contact immediately for details.  more...
From Dita Consulting
NEBOSH National Diploma in Occupational Health and Safety The NEBOSH Diploma is the leading qualification for UK health and safety practitioners. The NEBOSH Diploma builds on the knowledge gained at Certificate level and is designed for those seeking a successful long-term career as a health and safety professional. Benefits of holding the NEBOSH Diploma include: a Allows you to use the letters 'DipNEBOSH' after your name a Entitlement to graduate membership of IOSH (GradIOSH), the first step to becoming a Chartered Health and Safety Practitioner a Entitlement to full membership (MIIRSM) of the International Institute of Risk and Safety Management (IIRSM)) a Meets the entry requirements for many safety related Masters programmes offered by UK universities  more...
NEBOSH Oil Gas Certificate The NEBOSH International Technical Certificate in Oil and Gas Operational Safety is designed specifically for those with safety responsibilities in the oil and gas industry. It focuses on international standards and management systems, highlighting the importance of process safety management in the oil and gas industry, enabling students to effectively discharge workplace safety responsibilities both onshore and offshore. The NEBOSH Oil and Gas Certificate is suitable for those who have the responsibility for ensuring safety as part of their day-to-day duties, including: a Managers, supervisors and employee representatives within the oil and gas industry. a Newly-appointed health and safety advisers.  more...
NEBOSH National Construction Certificate The NEBOSH National Certificate in Construction Health and Safety has been designed to provide individuals making day-to-day decisions in construction work with the knowledge they need to ensure that the health and safety implications of their decisions are properly taken into account. It is suitable for: a Managers, supervisors and CDM co-ordinators within the construction industry. a Those who manage contractors. a Those who work in industries where temporary workplaces are a feature, e. g. utilities, broadcasting, etc. The NEBOSH Construction Certificate is widely respected by employers and meets the requirements for Technician Membership of IOSH (Tech IOSH) and Associate Membership of IIRSM (AIIRSM).  more...
NEBOSH International Fire Certificate The NEBOSH International Certificate in Fire Safety and Risk Management teaches how to carry out fire risk assessments and identify the range of measures needed to minimise the risk of fire. It helps holders manage risk more effectively and is ideal for: a Managers, supervisors, employee representatives a Those with fire safety responsibilities a Those looking to take on fire safety advisory roles The NEBOSH International Fire Certificate is widely respected by employers worldwide and meets the requirements for Technician Membership of IOSH (Tech IOSH) and Associate Membership of IIRSM (AIIRSM).  more...
NEBOSH National Fire Certificate NEBOSH National Fire Certificate The NEBOSH National Certificate in Fire Safety and Risk Management teaches how to carry out fire risk assessments and identify the range of measures needed to minimise the risk of fire. It helps holders manage risk more effectively and is ideal for: a Managers, supervisors and employee representatives a Those with fire safety responsibilities at work a Those looking to take on fire-safety advisory roles The NEBOSH Fire Certificate is widely respected by employers and meets the requirements for Technician Membership of IOSH (Tech IOSH) and Associate Membership of IIRSM (AIIRSM).  more...
NEBOSH Health and Well-being Certificate The NEBOSH National Certificate in the Management of Health and Well-being at Work gives managers, supervisors and HR personnel the skills and knowledge to tackle health and well-being at work. The course will benefit companies in all sectors who are seeking to improve the efficiency and morale of their workforce. It is suitable for: a General managers, supervisors, health and safety and HR personnel who have responsibility for, or involvement in, the health and well-being of employees as part of their day-to-day duties  more...
NEBOSH International General Certificate The NEBOSH International General Certificate in Occupational Safety and Health is an excellent foundation in occupational safety and health for all types of organisations. It helps holders manage risk more effectively by covering a broad range of topics and is ideal for: a Managers, supervisors, employee representatives a Those looking to start a career in health and safety The NEBOSH International Certificate is widely respected by employers worldwide and meets the requirements for Technician Membership of IOSH (Tech IOSH) and Associate Membership of IIRSM (AIIRSM).  more...
NEBOSH National General Certificate The NEBOSH National General Certificate in Occupational Health and Safety provides an excellent foundation in occupational health and safety. It helps its holders manage risk effectively by covering a broad range of topics, and is ideal for: a Managers, supervisors and employee representatives. a Those looking to start a career in health and safety. The NEBOSH Certificate is widely respected by employers and meets the requirements for Technician Membership of IOSH (Tech IOSH) and Associate Membership of IIRSM (AIIRSM).  more...
NEBOSH Diploma in Environmental Management NEBOSH Diploma in Environmental Management The NEBOSH National Diploma in Environmental Management is based on UK law and provides a detailed understanding of environmental risk management. The course is designed for those with responsibilities for the management of environmental risk or who are aiming to develop and implement effective environmental management systems within their organisations. Benefits of holding the NEBOSH Environmental Diploma include: a Allows the use of the letters 'EnvDipNEBOSH' after your name a Entitlement to Specialist membership (SIIRSM) of the International Institute of Risk and Safety Management (IIRSM) a Eligible for Practitioner Membership of IEMA (PIEMA) a Meeting the academic requirements for non-chartered Membership of the CIWEM (MCIWEM)  more...
NEBOSH Environmental Certificate The NEBOSH Certificate in Environmental Management provides a good overview of environmental management systems, including the relevant international standards and best practices for control of environmental hazards. It is suitable for: a Managers, supervisors and employees who have a responsibility for managing environmental issues. a Those looking to start a career in environmental management The NEBOSH Environmental Certificate is widely respected by employers worldwide; holders are eligible for: a Associate Membership of IEMA (AIEMA) a Technician Membership of CIWEM (TechCIWEM) Course Content The NEBOSH Environmental Certificate is made up of two unit: Unit EC1: Management and Control of Environmental Hazards a Foundations in Environmental Management a  more...
From TrainHr
How To Be A Better Proofreader This is the ideal webinar for anyone responsible for overseeing outgoing correspondence, paperwork, project proposals, and email throughout the course of the workday. You'll walk away with two tangible proofreading tools designed to make your job easier.  more...
Reputation Management What do your patients find when they Google you? An effective online marketing strategy encompasses much more than just a website. This program is designed to aid physicians and managers to understand the tools you will need to use to attract new patients to the practice, retain existing ones while creating and keeping a positive on line reputation and successful strategies to counteract negative reviews including litigation.  more...
Workplace Investigations Many employers struggle to gather information during witness interviews in investigations. Many employees for a variety of reasons are reluctant to be involved and can be less than forthcoming. Friends of employees and those accused of an offense are often downright angry and vengeful. In investigations, to meet its employer obligations, it's crucial that interviews are structured to capture and gather all available accurate information, notwithstanding employee emotions that are often running high.  more...
Time And Task Management The speed of everything has changed. Are your time management skills up to the challenge? Do you put off more today than you can ever accomplish tomorrow exhaust yourself by 4: 00 p. m. with only a fraction of your work done see yourself as a decision maker who never gets around to making decisions dread the next business meeting or worse, going back to your desk to see what voice mails and emails await you? If you're doing more and enjoying it less, it's time to get out of the time trap and back to productive management This presentation gives you practical techniques for controlling time and making it a manageable resource.  more...
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