Aspects to Consider For Clean Room Qualification And Operation – Webinar By Globalcompliancepanel

Overview: Controlled environmental conditions are often used when making medical devices and pharmaceuticals. However, to make sure these clean rooms are continuously operating in a state of control can be a difficult task unless the appropriate controls are incorporated into the design.

This talk will focus on the controls that need to be considered during the design and contruction and the methods to demonstrate these controls are effective.

Areas Covered in the Session:Clean Room Classification Design and OperationEngineering and Budget ConsiderationsAir Filtration and Maintaining Positive PressureInterlocks and Pass ThroughsControlling Human FactorsAcceptance CriteriaWho Will Benefit: This discussion will benefit any organization that wants to improve the control of their current clean room faclity or those considering building or upgradeing their clean rooms. It should be of interest to:QA and Manufacturing ManagersEngineersSupervisorsconsultantsAuditors

Tony has BS degrees in Biology & Microbiology and a MS in Quality Management. He is currently Quality Manager at Sealed Air, a supplier of rigid medical device packaging solutions. Previously he was Quality Systems Manager at Davol, Director of Quality Assurance at Scott Laboratories and Sr. Microbiologist at the National Cancer Institute. He is a Certified Quality Auditor-BioMedical and Certified Manager of Quality and Organizational Excellence by the American Society for Quality. He also teaches the refresher courses for these certification programs through the local RI-ASQ section. Tony has over 20 years experience using quality management techniques and value added auditing including the use of Failure Investigation and Root Cause Analysis to improve processes and products

GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.

GlobalCompliancePanel offers a broad range of channels for broadcasting and exchange of information through web based training, web alerts & discussion forums.

GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management. Apart from providing excellent training to compliance professionals by compliance & consulting experts, GlobalCompliancePanel would also focus on providing:

Information to ensure compliance and enhance quality with regulations for individuals as well as the organizationsLatest updates on industry trends, industry best practices and any modifications in the regulatory affairsOne stop destination for all your queries and to share and discuss issues, ideas and best practices andA resource on the data sheets, whitepapers, articles, books on industry standards, training kits, software tools, insights, press releases, etc on governance, regulatory, compliances and quality management across different industries.

Tuesday, May 15, 201210:00 AM PDT | 01:00 PM EDT

Price List:Live : $245.00Corporate live : $995.00Recorded : $295.00

webinars@globalcompliancepanel.com

Phone: 800-447-9407Fax: 302-288-6884

5 SEO Service Rules Every Law Firm Must Have In Mind

The third decade of the new millennia is on our doorstep and the internet is not slowing down with taking over every segment of our lives. From food to security of our homes, everything is connected and provided with the help of the internet.

Legal service is just another of the many society branches that found the internet and the search engines useful. Before, people had to take advice from friends and family to find a good lawyer. They had to list through the phone book to find their address. Today, this is no longer needed as every information is just a click away.

Billions of people are using the internet and almost everyone in the USA is connected. Law firms are available through it and with a simple search online everyone can find the nearest lawyer.

This is why law firms started investing more in this game. Their pages and social network profiles are being optimized for the clients and their needs. If you own a law firm, read about what are the most important rules of optimizing your page to get more clients.

1. Location must be highlighted

Local SEO for law firms is everything. As we just said, everyone’s on the internet now. This goes for clients and for the companies too. Everyone wants a piece of the action.

Google and the rest of the search engines are now much more focused on the location of the companies and the clients than ever before. The reason for this is that so many pages are offering the same results all around the world that having proper and reliable content means nothing.

That’s why the bots started favoring the ones that are closer to the location of the person searching. Everything is connected to the satellites and locating the search source is very easy. With it, the bots will give them the most relevant information in the sense of location.

If you want your company to be on top of the search list, the team taking care of the SEO must provide some keywords that will help the bots include your page into the list of perfect sources. This and some other features are important to make it to page 1.

2. Content must be useful

They always say – content is king. It’s the most important part. If you have no reliable content, the search engines won’t take you seriously and won’t offer your page to people who are searching.

The system is complex and only the people creating the bots understand it completely. However, it is well known that you can’t just align a few words that make no sense and expect to rank high. Your articles and pages must offer something valuable to the people searching online.

You can do a perfect job with every single detail containing the SEO, but if you don’t offer quality content and information that is being searched for, you won’t get anywhere.

3. Your page must be optimized

Back in the day, there was no option about the device that someone is surfing the net. It was a desktop computer. Today, the options are numerous. People get online through desktop computers, laptops, tablets, and smartphones.

All this means you need to optimize your page for all these devices if you want people to have a great view of your content. More important, you have to do this to rank higher on the search engines. They’ll see if you use the same platform for every device and if you haven’t suited it, it will put your page lower on the engine.

4. Speed everything up

Research showed that pages who are slow are not going to make it high in the results. It is the number one on every list of things that people absolutely hate when opening a page.

This means you have to do something about for two reasons which are equally important for your business. First, you need to speed it up because people will hate waiting for your information that takes forever to load, and second because it will automatically be put out of the competition by the search engine bots.

To do this, you’ll need to do some things that probably need to be done by an expert. Things like choosing smaller pictures, changing parts of the code that are doing problems, and turning off pop-ups, banners, and everything that may be slowing it down.

If your entire page loads more than 10 seconds you can be sure that you’re having trouble. Most pages are loading around 7-8 seconds, but it’s best if you can manage to get under the limit of 3 seconds. If you can do this, be sure that you’ll be going up on the rankings. See more reasons why people bounce off here.

5. Keywords must be perfect

The keyword game also changed a lot over the years. People used to search for only one word, for example, lawyer. As the internet becomes a global thing and every lawyer on earth become available on the internet, people started searching for a specialized one, for example – DUI lawyer.

Now, the most probable way of searching is including the industry, the specialization, and the location. Most people will probably search DUI lawyer Houston, if they are looking for an attorney who will represent them after they were caught drinking and driving in Houston, Texas.

Paying a lot of attention on keyword research and using them inside your articles and page is very important. Always make sure the keyword is inside your title and the content too. It’s a matter of strategy how many times it will be used, but this is something that professionals will need to give their opinion.

Conclusion

If you learn and use these 5 rules, you can be sure that your lawyer-themed web page will be ranked on Google and the other engines. Achieving this will be great for your business.

All about Personal Injury Lawyers: An Introduction

Personal injury attorneys are a type of litigator who provides legal any form of legal representation to people who are alleging psychological or physical injury as the result of a careless or negligent act of another entity, individual, organization or person.

Personal injury and tort law are all the same

Personal injury lawyer specialize in the area of law known as tort law. It covers civil or private wrongdoings or injuries, including action and defamation for breach of contract. The primary goal of the tort law is to make the injured person get the compensation that they deserve. Not only that, it discourages other people from committing the same violation. 

Personal injury attorneys help the injured party receive compensation for their losses. It includes the loss of financial earning capacity because of their inability to work, compensation for their suffering and pain. These legal counsels will also help the injured party get reasonable medical expenses for both expected and present, loss of consortium or companionship, legal fees and legal costs and emotional distress. 

These attorneys also work to protect clients from being victimized by their insurance company, and most notably, screwed by the legal system.

Types of cases considered as personal injury

Any claim or case that involves injuries to the mind or body falls under personal injury law. Listed below are the most common types of personal injury cases that are usually handled by personal injury legal counsels. It includes:

Automobile and motorcycle accidents

Injuries from an animal bite

Aviation accidents

Boating accidents

Accidents when riding a bicycle

Brain trauma

Damages from fire accidents like burns

Accidents from construction sites

Accidents from defective products

Bad faith and insurance claims

Medical malpractice

Abuses from orphanages and nursing homes

Pedestrian accidents

Fall and slip accidents

Injuries in the spinal cord

Wrongful death

To find out more about personal injury, you can check out https://en.wikipedia.org/wiki/Personal_injury

What do these personal injury lawyers do?

Legal counsel who specialize in this area of the law, handle cases from the get-go through appeal. They do the same task as most litigators. They usually investigate any claims and screen any potential clients to evaluate the advantages of the case they plan to handle. The legal counsel gather evidence, research case law and formulate a legal theory. 

Their job involves drafting a plea deal, motions, as well as, discovery any form of requests and interviewing or deposing all possible witnesses. All the tasks can contribute to the trial preparation, although the job does not end there. Personal injury lawyers usually juggle a lot of caseloads at the very least, and it is the ideal workload for most lawyers. 

These type of legal counsels serves as a legal advocate of their clients before, during and after the trial. It can include giving them counsel, as well as dealing with any forms of obstacles in the legal system. They will also defend their clients from evidence and witnesses presented by the other parties. 

Personal injury cases can be very complicated; that is why these lawyers usually specialize in certain types of legal matters. For example, lawyers who handle medical malpractice might focus or specializes in breach births. Those lawyers who regularly handle motor vehicle accidents might focus on ATV rollover incident or accident cases.

If you want to know why legal counsel need to do specialization, click here.

Required education

All lawyers need to pursue the same path of education and training. They need to earn their degrees and pass the bar examinations, but it cannot be accomplished until they have earned an undergraduate degree and passed the LSAR or the Law School Admission Test with a reasonably high score. 

Attorneys can become certified as a specialist in civil trial advocacy by finishing a specialty certification course, accredited by NBLSC or the National Board of Legal Specialty Certification. It is a non-profit group or organization certified by the ABA or American Bar Association to give board certificates to passing lawyers. 

A lot of these bar associations also require personal injury attorneys to pass the MPRE or the Multi-state Professional Responsibility Examination, who emphasizes on professional behavior. The state also needs to require the professionals to take additional programs and continue learning from education courses.

Professional and personal skills

Most successful injury legal counsels excel at negotiations, client development and oral advocacy. They also need to have a capacity to handle pressure and stress, especially those who want to hang their name on the wall instead of being an associate to an existing law firm. Lawyers who consider themselves as specialist usually represent their client on an occurrence basis. 

The lawyer’s fee represents a percentage of the complainant’s eventual compensation when they resolve the case, usually from 30% to 40%. The arrangement means that the complainant does not pay a fee until and unless the legal counsel recovers the money on their behalf. These counsels are only compensated if the case is won, most of the time. 

That is pressure when you consider some injury cases can drag out for months or even years before they are resolved. Lawyers must have adequate time management skills. You would have to balance shorter and less demanding cases with long and involved ones if you are going to pay the bills if you decided to go into practice by yourself. 

It is usually recommended that new injury lawyers need to get their feet wet and become a worker to more established law firms before they head out on their own. It will help them understand everything about legal cases and how your opponent’s approach to the cases. 

Want to know how much attorneys usually charge their clients? Click here for more information.

How much are personal injury attorneys earning?

Personal injury attorneys are considered as one of the highest-paid professionals today. The most successful legal counsels can earn at least seven-digit salaries per year, although most attorneys can earn from $30,000 to $300,000, depending on their location of practice and specialty. The average salary of a lawyer ranges from $100,00 to $500,000 per year. 

Plaintiff attorneys who have a higher lawyer fee usually handle high-profile class action suits or high-profile personal injury cases. Not only that, claims that are designed to punish defendants or also called punitive damages, can raise decision amounts by at least a million-dollar, adding money to the counsel’s 

EMC Test And FCC Compliance Are Two Words to Keep in Mind For Electrical Device Manufacturers

EMC test and FCC compliance are two very common phrases for all those that are involved in the manufacture of electrical and electronic devices. It is common knowledge that these devices often produce radio frequency and this can have multiple harmful effects. Through testing and compliance a manufacturer can avoid such circumstances and release their products to the market in the shortest possible time. And this is important given the intense competition that is there in this industry.

What is EMC? This is one question many people tend to ask. EMC or Electromagnetic Compatibility is a science that deals with the unexpected generation, propagation and reception of electromagnetic energy. EMC certification is widely sought out by the manufacturing companies that produce wireless and medical equipment.

Along with EMC there is another phrase you will come across. This is called EMI or Electromagnetic Interference. It is a common phrase in the electronic product manufacturing industry where statute says that any electrical or electronic device shouldn’t interfere with another electrical or electronic device in its vicinity. EMI and EMC are tests that can be conducted easily by experts. Issues like radiated emissions and radiated immunity can be taken care of by EMI testing and EMC testing.

FCC or Federal Communications Commission is an independent US federal agency and it works in the areas of broadband, competition, homeland security, media, public safety and the spectrum. Any new product that is manufactured and that falls under these six categories need to comply with the relevant part of Title 47 of the US Code of Federal Regulations. FCC compliance is needed for all these products and without the compliance certificate the product cannot be released to the market.

While there are many requirements of FCC compliance, one of the most important among all is FCC part 15. This can be received after the compliance testing is done and the product clears the test. Like EMC test, FCC testing can also be done by an independent agency and they can help you get the certification for your product.

Why do you need EMC test and FCC compliance? The reason is rather simple to see – without EMC and FCC certificates your products cannot be legally released to the market. You spend thousands of hours and significant money and staff time to develop a product. It is but obvious that you would like to release it for sale ASAP so that it starts bringing in the revenue. When your product doesn’t clear these tests you need to wait for retesting. And retesting means more money and time lost. You wouldn’t want this, would you?

When you work with a professional agency for EMC test and FCC compliance you can rest assured that your time to market will be as low as possible. They not only prepare your product for the tests but also ensure that the initial problems are taken care of and there is no requirement for retesting.

EMC test and FCC compliance are absolutely required and you shouldn’t compromise with them at any cost.

Understanding The Importance And Functions of Reach Compliance

With the increasing competition in the market, the organizations into manufacturing products comprising of chemical substances have certainly lead to increase in pollution in the environment. It is not only harming people in many ways, but is also affecting the real beauty of our nature. But, with steps like REACH Compliance, things seem to be moving towards a new direction.

REACH is basically a new European Community Regulation on chemicals and their safe use. It targets at dealing with the Registration, Evaluation, Authorization and Restriction of Chemical substances. The law that came into force on 1st June 2007 has come up with an aim to improve the protection of human health and the environment through the better and earlier identification of the intrinsic properties of chemical substances. At the same time, it also targets at enhancing the innovative capability and competitive of the EU chemicals industry.

The benefits of REACH software are very much palpable in the environment as it gives greater responsibility to the industry to manage the risks from chemicals and to provide safety information on the substances. Here, with its regulation, the manufacturers and the importers will be required to gather information on the properties of their chemical substances, which allow safe handling of them.

But, the biggest challenge is to understand and follow the legislation because it sounds confusing. In simpler words, REACH obligates manufacturers in the EU to ensure the chemicals it is using in excess of one ton annually are registered with a new central chemical agency set up in Helsinki and Finland. Here, the registration carried by the manufacturers includes supplying data such as chemical types and uses, volumes per annum and test data results.

It also compels companies importing products to ensure that the substances present inside those products are registered. However, if the manufacturer ensures that no one will be exposed to the substances during its use, including disposal, then it is not required to go for the registration.

The complexity of REACH compliance lies in its difference from nearly every company. For instance, each legal state has its different set of requirements and the company many also split into five legal entities each using less than one ton of a chemical per year. Moreover, it can also be done under one entity, in which case the tonnage is added together and falls under the scope of RACH.

So, look no further and move ahead in cleaning your environment and making it a chemical free place to live by getting a simple registration with REACH.

Defence For Disqualified Directors Orders

You may be experiencing the Insolvency Service laying the claim that one of your directors (or yourself) is a disqualified company director.

But it must prove that the director in question is unfit to continue with his or her duties. So anyone facing the prospect of being banned from continuing with their duties for a period of time should seek specialist legal advice.

Any proceedings for disqualified company directors are initiated under the Directors Disqualification Act 1986. It was this act which introduced the concept of unfit directors and their disqualification. The process is adversarial so it is always in director’s best interests to seek advice and representation from solicitors who specialise in disqualified directors cases.

There are various reasons why people may be ruled disqualified company directors. They might have allowed the business to continue trading while it was insolvent. This will have put any creditors at a severe disadvantage. They may have persistently breached legislation covering companies, such as by failing to keep proper books and records. A director may also be disqualified if he has allowed his company to use a prohibited name. Or he might have failed to co-operate with the company administrator or liquidator. Another reason for disqualification may be the fact that the director has failed to lodge tax returns or pay taxes due.

Whatever the reasons for people facing the prospect of becoming disqualified company directors, it cannot be overemphasised that the onus of proof is on those seeking disqualification. But this does not mean that those facing an order should just sit back. They need to pro-active and that means consulting with lawyers who deal with such cases.

If there is a defence against being named as a disqualified director the solicitor will help identify this. The defence will be put in a ‘Statement of Truth’ which will be put, under oath to the court. Defence witnesses may also be called. The aim is to dispel any suggestions that the director has been negligent in his duties, or is unfit to carry on his role in the business.

Even if, following consultations with the solicitor, that there is no realistic defence, there may be a chance to shorten the term of any disqualified directors ban by pleading there were mitigating circumstances. It is very important, if need be, that this course of action is followed as the consequences for disqualified company directors are so severe.

Disqualified directors cannot continue their role with their current company or form another one. Their names will also appear on the Disqualified Company Directors Register which is available to the public.

Online Will Kits Got Your Attention? Think Again!

Online advertisers are getting better with their lure of helping you make your will using cheap software or template will kits. Wills are not so trivial and you should take these more seriously. If it were a simple application or a draft of something not as significant, you could have easily relied on software, but much more is at stake here. A single mistake with the signature or a miscalculation with the most unassuming number can spoil all your hard work and make your intestate.

Advantage of Hiring Estate Lawyers

Estate lawyers give you highly personalized advice on your wills and estates, which you will never find with do-it-yourself kits. These kits advertise that anyone with a basic high school education can fill in the blanks and get their wills made, but what they hide is that someone with a high school education may not know much about state estate laws.

A will kit addresses the most common and mundane issues of a will. It does not provide for complications that may arise after your demise. To illustrate let us take the example of tax returns, if something does not pan out the way your will-kit provided for, then your benefactors will be at the deep end of the pool with a long legal battle ahead of them. In short, in an attempt to save a few hundred dollars you will push your family into the uncertainties of legal tussles.

To get all your loose ends in order you will require the professional service of an estate lawyer.

Without a real person to help you with your will, there cannot be peace of mind. Do-it-yourself kits come with no liabilities and will not bear any responsibility if the testator misinterprets a clause or makes the wrong choice for the lack of foreseeing the outcomes of his actions.

A common practice among users of such kits is to get their forms checked by Estate lawyers. The service of an estate lawyer does not come for free and the charges are just shy of a full blown will making session. Therefore, we think it is only wise to walk into the office of an estate lawyer and get your will made in the most professional manner possible.

How to Prepare For Manage And Follow up to an FDA Inspection – Webinar By Globalcompliancepanel

The FDA inspection is the most nerve-wracking event in the life of a regulatory professional – you’re in charge of compliance, usually in the background, and NOW you’re in the spotlight, and if your performance is not good, it is not the show that may close, it is YOUR COMPANY! However, adequate planning, training, composure, and understanding should result in many encore presentations!

This session will discuss how to prepare for the inspection, what to do during the inspection and the close-out interview, and how to respond to the inspection. Also contained in this session will be the limits of FDA’s scope during an inspection, including what documents you are not required to show them, and the permissibility of photographs and affidavits.

Areas Covered in the Session:

Who Will Benefit:

Price List:Live : $245.00Corporate live : $995.00Recorded : $295.00

webinars@globalcompliancepanel.com

Phone: 800-447-9407Fax: 302-288-6884

Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy products. In this position, Jeff is responsible for supplier management, during which he reviews and approves supplier qualification, selection, assessment, and CAPA. Prior to this, Jeff spent 13 years at Life-Tech as the Director of Regulatory Affairs, where he was responsible for regulatory compliance of all aspects of the quality system. Jeff received his regulatory affairs certification in 1996.GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.

GlobalCompliancePanel offers a broad range of channels for broadcasting and exchange of information through web based training, web alerts & discussion forums.

GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management. Apart from providing excellent training to compliance professionals by compliance & consulting experts, GlobalCompliancePanel would also focus on providing:

EU Medical Device Classification – Webinar By GlobalCompliancePanel

Why should you attend : Today, medical devices occupy an extensive range of products that vary in intricacy and application. As the global market for medical devices continues to grow, it is important that companies be informed on the rules for classification of medical devices because of potential risk that can be associated with the device can have on the human body when used. This webinar will discuss the application of EU Council Directive on medical device classification.

Areas Covered in the Session

Basic definitions and purpose of medical device classification

How to carry out classification by reviewing the application and how to use the classification rules

Explanation of individual classification rules regarding non- invasive and invasive devises, along with additional rules applicable to active devices and other special rules

Who Will Benefit:

Quality Managers and Professionals

Marketing Managers and Professionals

Risk Managers and Investigators

R&D Project Managers and Team Members

Design Engineers

Consultants

Joy Frestedt, PhD, CCTI, RAC, FRAPS. Dr. Frestedt is the President and CEO of Frestedt Incorporated, a novel virtual Contract Research Organization network of over 50 experts and highly skilled staff meeting specific needs in regulatory, clinical and quality affairs. Dr. Frestedt has over 30 years of scientific, clinical and regulatory experience in the health care, pharmaceutical and medical device industries especially running clinical trials, conducting laboratory analyses and assisting firms with strategic decisions involving clinical research programs, regulatory strategies and the development of quality systems to compete globally. She has held key positions including vice president of scientific, regulatory and clinical affairs at BridgePoint Medical and Humanetics Corporation as well as key management positions with Johnson and Johnson’s Ortho Biotech, Medtronic, Mayo Clinical Trial Services, AstraZenca Pharmaceuticals and Orphan Medical. Dr. Frestedt holds a B.A. in biology from Knox College and a Ph.D. in pathobiology from the University of Minnesota Medical School and she is a member of the American Society of Clinical Oncologists, American Association of Pharmaceutical Scientists, American Society of Clinical Research Professionals and she is a Fellow of the Regulatory Affairs Professionals Society. Dr. Frestedt was named one of the “100 Most Inspiring People in the Life Sciences Industry (by PharmaVOICE, 2011) and one of the top 25 “Industry Leaders/ Women in Business Award (by the Minneapolis/St. Paul Business Journal, 2011).

GlobalCompliancePanelwww.globalcompliancepanel.comwebinars@

Click here for More Details

Phone: 800-447-9407 Fax: 302-288-6884

Why Compliance Management System is Important

The need for ethical business administration in a corporate environment is very crucial. Several key corporate issues such as company risk, governance and compliance are faced by companies. In the past, some firms have cared less for ethical administration and entangled themselves with several issues that have posed a threat to the economy. Companies don’t want to get trapped within such worrying issues and are more careful nowadays. Thankfully credentialing services provide them plenty of tools to manage their business effectively.

In the wake of the dwindling economy and growing concerns over corporate governance and compliance, many governments of first-world nations have unleashed stringent laws to monitor company operations. This gave companies more reasons to have a streamlined corporate governance system and so a strong emphasis on credential evaluation has been laid upon. Today, many businesses are investing in a compliance management system to ensure a bright future for their organizations. A good credentialing system helps businesses manage documents, licenses and certifications efficiently.

In order to tackle compliance issues, companies must first make themselves aware of the consequences of non-compliance. Along with managing business operations, companies often face the problems of managing documents related to corporate governance, risk and compliance. Managing these documents can be tiresome, thereby affecting the management and to some extent, the profitability of a company. Most companies now have a streamlined management system, thanks to credentialing services.

A compliance management system helps organizations stay compliant and manage employee credentials with ease. Companies have highly skilled employees whose licenses, insurance and certifications need to get updated regularly. A credentialing system helps companies keep all documents up to date and hence meet their compliance goals.

Companies that don’t have a proper compliance management system fail to keep all documents updated. This can lead to outdated or fraudulent employee credentials and can be a serious issue during audits. If law enforcers find any malpractices in an employee’s credentials, then the entire company might be held liable for such mismanagement, leading to serious consequences. Organizations investing in good credentialing services need not worry. They have an excellent web-based software program that manages their credentials and help them comply with all rules and regulations laid down by the corporate laws.