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Search Results - Compliance Training

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Showing 1 to 25 of 189 Articles matching 'Compliance Training' in related articles.
Pages: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | Next >>

1. The FTA: Your Fleet's Friend On and Off the Road
May 24, 2018

The UK’s Fleet Transport Association (FTA) is a huge organisation with a significant number of members, all of who are involved in haulage work in some capacity. When you consider the support it affords its members in terms of compliance training, advice and certification, it’s perhaps not surprising that over 50% of the UK’s HGV fleetsand at least a million vans are involved with the association.Part of its valuable work also involvesrepresenting haulage workers’ views by lobbying policy makers. Below is an overview of what the FTA membership offers. Compliance Our industry is... (read more)

Author: Laura Jeeves

2. Gold Coin Garage Door Repair Katy Hired Licensed and Insured Technicians to Expand Their Workforce
January 05, 2018

Katy, Texas - In a bid to become a top-flight garage door repair service provider in Katy, Texas, Gold Coin Garage Door Repair Katy TX recently recruited a number of licensed and insured technicians. The owners of the garage door repair service shop said that the insured and licensed technicians have all gone through months and years of on-site training and have received their certification after proving their efficiency in compliance with the guidelines provided by the American garage door repair technician organizations. Gold Coin Garage Door Repair Katy is all set to offer on-job tra... (read more)

Author: John Doe

3. Putting an effective complaint and recall management system in place
October 31, 2017

Complaints very strongly show a company how its products or services are perceived where it matters the most -in the customer’s mind. Complaint handling is one of the key indicators of how seriously a business takes its customers’ point of view. Complaints are to be expected from about any product; but their importance is all the more felt in an area like medical devices, because these products can affect the very life of their users. In the context of medical devices; complaints are any communication made in writing, electronically or in verbal form about any of these aspects of a medical... (read more)

Author: John Robinson

4. FTA Launches New Awards for Supply Chain Excellence
October 02, 2017

The FTA has recently announced its latest awards, which will recognise excellence in supply chain leadership. Who knows – maybe you’ll be a winner! About The FTA As you probably already know, the Freight Transport Association, or FTA, is one of Britain’s biggest and oldest trade associations, operating over 200,000 lorries. With their four key priorities (representation, campaigning, compliance and training), the FTA has been delivering “safe, sustainable and efficient logistics” for almost 130 years. The New Awards The FTA Logistics Awards celebrate the best transport i... (read more)

Author: Laura Jeeves

5. Online Course Offer 2017 by GlobalCompliancePanel @ 10$
September 14, 2017

Not come across the online course offer 2017 by GlobalCompliancePanel @ 10$ yet? You don’t know what you have been missing. First of all, what is this online course offer 2017 by GlobalCompliancePanel @ 10$ about? Is it about any other of the thousands of products that are available in the market for $10? No way! This online course offer 2017 by GlobalCompliancePanel @ 10$ is about the unlikeliest of products that you could pay $10 for: Webinars that offer regulatory trainings! What? A training webinar, that too on such a niche area as regulatory compliance, at all of $10? Sounds incredulous, ... (read more)

Author: John Robinson

6. Become Compliance Expert; Pick Any Webinar Just for $10
August 17, 2017

GlobalCompliancePanel offers what should rate as an opportunity of a lifetime: To become compliance expert; pick any webinar just for $10! With the extremely strict regulatory compliance requirements set out by the FDA and other regulatory agencies such as the EMA; professionals who work in the regulated industries are at their wit’s end in determining what kind of training they need to understand the regulatory requirements and comply with them. With this offer by which regulatory professional can become a compliance expert by picking any webinar just for $10; GlobalCompliancePanel makes th... (read more)

Author: John Robinson

7. Webinar Special Sale 2017 by GlobalCompliancePanel for just $10
August 16, 2017

Wondering which course to take up to augment your regulatory career? Is the steep price of these trainings a deterrent? It need not be so anymore. GlobalCompliancePanel, a leading provider of professional trainings for the regulatory compliance arena, has announced an offer that will take some time to digest: Regulatory training courses for a throwaway price of $10! If this small number has befuddled you, be prepared for a greater surprise, this time with higher numbers: Over 500 such courses are on sale. Could there be a more special sale? Imagine the amount you have to spend for staying up... (read more)

Author: John Robinson

8. Launch of New Training Course from Legionella Experts Brings Essential Skills In-House
June 09, 2017

As the risks associated with legionella continues to rise around the world, experts Legionella Control have launched a new course that could help companies save money and maintain compliance. Using their in-depth insight, the company is offering ten practical training modules covering water safety monitoring and maintenance for water systems that firms will be able to sign existing members of staff up for. Legionella bacteria, which can lurk in any manmade water system, has the potential to cause Legionnaires’ disease. The disease can lead to life threatening pneumonia-like infections and o... (read more)

Author: John Doe

9. The UK's Driver CPC Training Post-Brexit
March 01, 2017

Anyone working in the UK transport industry will be aware of the need to keep abreast of up-to-date changes and opportunities in HGV driver training and, in particular, the importance of compliance with regards to the Driver Certificate of Professional Competence (Driver CPC). The Freight Transport Association has expressed concerns that proposed revisions to the CPC by the European Commission post-Brexit will have an impact on drivers receiving adequate and relevant training. Current Driver CPC Training The primary aim of the compulsory Driver CPC is to increase road safety and aw... (read more)

Author: Laura Jeeves

10. Full value at half the price from GlobalCompliancePanel for this Christmas and New Year
December 04, 2016

Professionals in the areas of regulatory compliance and Regulatory Affairs have an added reason to celebrate Christmas and New Year. GlobalCompliancePanel panel has served them a great offer by which its professional training courses will be offered at half the original price. Starting from today and doing up to January 1, 2017, regulatory professionals have a very solid reason to celebrate the festivities. GlobalCompliancePanel is offering a blanket 50% off on all its seminars. Details of the offer What this means is this: For webinars that are slated for any announced date, there will b... (read more)

Author: John Robinson

11. Tips for and with health and safety in scaffolding
November 21, 2016

Working on a scaffold can be a dangerous job if it is not in compliance with proper safety standards. Workers should strictly comply with the safety procedures so that they can get their work done without any sort of accident. Following are some safety law, duties and responsibilities outlined by officials for employers, supervisors and workers regarding scaffold safety: Well trained Staff Train all your staff in understanding and handling the design and the operation of scaffolding. Training should cover how to safely get on and off scaffoldings and it should also cover fall pr... (read more)

Author: Innes Donaldson

12. Adherence to GMP is absolutely essential for Quality Control and Contract Laboratories
November 21, 2016

It is absolutely essential for contract laboratories to maintain the required standards of Quality Control because of the risk their process involves: After testing and approval, drug products and Active Pharmaceutical Ingredients (APIs) are released to the market without further check. This fact is the primary reason for which regulatory agencies such as the FDA, EMA and many others place the highest emphasis and priority on inspections of QC laboratories. This is also one of the main reasons for which a huge number of QC related 483's and Warning Letters get issued to companies that have pr... (read more)

Author: John Robinson

13. A complete understanding of the payroll law
November 18, 2016

Those who are responsible for payroll or employer tax withholding compliance or have just been hired or promoted into the payroll department would have discovered during their indoctrination just how important this role is to the success of the organization. Their learning is a continuous process that goes on and on. Employees in this position need to build a solid foundation for handling their company's payroll obligations and complying with federal and state payroll laws. They need to be familiar with how to find the authoritative laws to support their policies and procedures. Clear and ... (read more)

Author: John Robinson

14. Identifying and managing key risks is the primary purpose of HR auditing
November 17, 2016

Human resources audit should qualify as the most important of all audits of an organization. This is because HR auditing is directly related to employees. This resource, the organization’s human capital, is the organization’s most important resource. It is through an HR audit that an organization evaluates this resource’s strengths and weaknesses. HR audits help organizations in a number of ways HR auditing helps organizations achieve this in many ways. Through HR audits, organizations are able to eliminate human capital risks, which will lead them to core actions such as ascertaining poten... (read more)

Author: John Robinson

15. An understanding of HIPAA upcoming changes for 2016
November 16, 2016

Professionals at various levels of the healthcare industry need to have a grasp of the HIPAA Security/Privacy Rule and the way it relates to their practice or business. A two-day, in person, live seminar being organized by GlobalCompliancePanel, a leading provider of professional trainings for the regulatory compliance areas, will offer this very important understanding. Brian Tuttle, a Certified Professional in Health IT (CPHIT), Certified HIPAA Professional (CHP), and Certified Business Resilience Auditor (CBRA) , who brings over 15 years’ experience in Health IT and Compliance Consulting,... (read more)

Author: John Robinson

16. Getting Design of Experiments and Statistical Process Control right for Process Development and Val
November 15, 2016

Procedures must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. Why this needs to be done is because the FDA has, in a recent guidance document on Process Validation, assigned the responsibility for reviewing and interpreting DOE and SPC studies to the Quality Unit. Going about doing this work requires a practical orientation. It calls for an approach with case studies and examples. A seminar that is being organized by GlobalCompliancePanel, a leading provider of professional trainings for the regulatory compliance a... (read more)

Author: John Robinson

17. Getting design controls right is absolutely essential for medical device companies
November 11, 2016

Design Controls are absolutely essential for ensuring the safe and effective production of medical devices. The FDA too considers design Controls a critical process. Yet, design controls are among the most frequently cited areas for 483 and Warning Letter observations from the FDA. Although intrinsic quality, safety, and effectiveness of a device are known to be established during the design phase; a significant percentage of all medical device recalls are due to design problems, as statistics show. The implications of poor design of medical devices controls are quite obvious: o They accou... (read more)

Author: John Robinson

18. Extracting Information from Geochemical Data
November 10, 2016

Going beyond just asking the laboratory for geochemical extracting information of a gold test by sampling every meter of the drill core of a trench and using multielement analysis is an approach strongly recommended by most mining specialists. There exist other methods of geochemical data analysis techniques and obtaining geochemical extracting information, but these are largely ignored by the industry. Making sense of the geochemical extracting information How to make sense of the geochemical extracting information is the core of a webinar that is being organized by GlobalCompliancePanel, ... (read more)

Author: John Robinson

19. Ways of conducting a hassle-free internal and supplier audit for medical devices
November 09, 2016

Carrying out efficient and effective internal and supplier audits that meet all the requirements of external auditors is a must for medical device manufacturers. These audits should not only serve this purpose; they should also add value to the medical device organization. Part of both ISO 13485 and QMS Internal audits are required as part of ISO 13485 and the FDA’s Quality System Regulation (QMS). However, these procedures are quite complicated for many professionals in the medical device industry. They are often confusing and cumbersome, mainly because of the jargon and regulatory langua... (read more)

Author: John Robinson

20. Article based on Effective and Efficient Internal
November 08, 2016

A 510(K) is a premarket submission made to FDA to demonstrate that a device to be marketed is at least as safe and effective, meaning that which is substantially equivalent, to a legally marketed device that is not subject to premarket approval (PMA). There are three types of Premarket Notification 510(K)’s that may be submitted to FDA: Traditional, Special, and Abbreviated. Product modifications that could significantly affect safety and effectiveness are subject to 510(K) submission requirements under 21 CFR 807 as well as design control requirements under the Quality System (QS) regulation... (read more)

Author: John Robinson

21. Article based on Applying ISO14971 and IEC62304
November 07, 2016

Diligent, complete and correct implementation of risk management of software used in medical devices that takes into consideration the gaps and corrects them from the start of product development is absolutely imperative. This is because of two critical reasons: 1. Gaps, incorrect or incomplete implementation can retard or delay or make the certification/approval of medical products impossible; 2. Since most activities are closely linked to the development lifecycle; almost none of it can be retrospectively performed. This renders all activities performed till the identification of gaps usel... (read more)

Author: John Robinson

22. Article based on Applied Statistics with Emphasis
November 02, 2016

Evaluating product and processes is an imperative for almost all design and/or manufacturing companies. These are the reasons for which this evaluation needs to be made: o Managing risks o Validation of processes o Establishing product/process specifications to QC to such specifications o Monitoring compliance to such specifications Lack of proper and thorough grasp of and correct implementation of statistical methods leads a company to having to face significant increases in its complaint rates, scrap rates, and time-to-market. As a result, such companies churn out poor quality in thei... (read more)

Author: John Robinson

23. Tools and Methodologies to Predict and Improve Product Reliability
October 27, 2016

Improving product reliability may be the primary objective of reliability analysis; yet, there are many possible reasons for collecting and analyzing reliability data. There are many examples of collecting and analyzing reliability data. This could be done to assess product reliability in the field. It could be to predict product warranty costs. It could be for estimating replacement part/spares requirements. Other examples of collecting and analyzing reliability data include: o To assess the effect of a proposed design change o To demonstrate product reliability to customers or government... (read more)

Author: John Robinson

24. Article based on Human Subjects Research Seminar
October 26, 2016

Protection of human subjects and everything relating to it is of paramount importance for those involved in or wanting to be involved in research dealing with human subjects or an individual's private identifiable information. For these individuals, professionals and companies, it is extremely important to understand that there are federal regulations that must be followed. There are also state statutes, institutional policies, federal guidance documents, and ethical codes that guide the conduct of the research. This is done to ensure that the research not only meets the regulatory requireme... (read more)

Author: John Robinson

25. Assessment-based prediction is an effective tool for hiring the right candidate
October 25, 2016

Assessment-based prediction is an effective tool for hiring the right candidate Undoubtedly, hiring should rate as being among the most important activities for an organization. This is so because it is through this process that the organization takes in its most important resource –people. At the time of hiring, as well as while considering promoting, HR and the other important decision makers need to make up their mind by asking critical questions with which to make predictions about a potential hire. These questions could relate to how well the resource can perform in the assigned role, fo... (read more)

Author: John Robinson

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