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Cup Junction

http://cupjunction.blogspot.com

Parties have become a part of day to day life these days. We work hard and love to enjoy the success what we get but in this series we forget few things, which become a big trouble in future for all of us. Sometimes we don’t give importance to disposable plates and cups and such ignorance becomes a big reason of pollution. If you are a responsible person and want to enjoy your party with full of fun, you should use disposable coffee cups Canada.


Najlepsze źródło informacji, aby dowiedzieć się kursy języka włoskiego

http://www.szkoly.puntoit.pl/blog/najlepsze-zrodlo-informacji-aby-dowiedziec-sie-kursy-jezyka-wloskiego

Coraz więcej szkół zamieszcza w swoich ofertach język włoski, chcąc urozmaicić program danej placówki, dzięki czemu w wielu warszawskich liceach nauka języka włoskiego stała się bardzo popularna.


Best Online Grocery Shopping Store | Online Supermarket

http://vijethaonlinesupermarket.blogspot.in

VijethaGrocer.com is a unit of Vijetha Supermarket Pvt.Ltd.With over 10,000 items from over 500 brands in our store.we had present 27 stores placed across Hyd &Vizag.Our online food store offers a variety of products across various categories like : Fresh Fruits & Vegetables, Grocery & Staples, Beverages, Bread,Dairy & Egg products, Branded Foods,Meat, Personal Care and Household products.


juanitasbiz.com

http://juanitasbiz.com

Health and fitness with Juanita learn how to better your health and wellness and lose weight fast with It Works Products.


Deborah Ferrari

http://deborahferrari.design

Deborah Ferrari is the one who changed the mind set of people that thing only Italian can cook delectable Italian food. She is a food blogger, television host, journalist and owner of some popular restaurants in all over the world. She was born in small town of Spain on 7th of October.


An Impromptu Sunday Lunch - Beyond360Pune

http://beyond360pune.blogspot.in

Experience Pune's fastest restaurant food delivery services with Beyond 360°. Enjoy 5 star-like gourmet food dishes designed by Chef Anand. Indulge in premium quality soups, starters, main course and desserts at best prices with leading best takeaway food and home deliveries in Pune. Bulk orders and corporate meal ordering also accepted.


Get Samsung Galaxy S6 edge-32GB at poorvika

http://goo.gl/OtmpoA

Introduction The bold, stunning and latest addition to the Samsung family, Samsung Galaxy S6 Edge is intended to supply you a revolutionary expertise. This Samsung flagship mobile deserves approval for being the world’s initial dual-curved glass Smartphone. Better Performance It has 3GB RAM capability and therefore the quickest non-volatile storage 2.0 that comes in numerous versions of 32GB / 64GB / 128 GB, Samsung Galaxy S6 Edge could be a mobile enthusiast’s mean machine. It’s powered by associate Octa-Core 64-bit Exynos processor.In straightforward words, it's lag-free and super-quick multitasking expertise for you.



Review of Apple Iphone 6- 16GB

http://goo.gl/ESGzts

iPhone 6 is n't just greater — it's better inside and out. Bigger, yet drastically more slender. All the more intense, however astoundingly control productive. With a smooth metal surface that flawlessly meets the new Retina HD show.


Apple iPhone 6S - 64GB Sprint Gold Platinum | Poorvikamobile.com

http://goo.gl/5bKMpV

Apple iPhone 6s is new top most level apple telephone. It conveys execution once discovered just in desktop. You will get information up to 70 percent speedier CPU execution, and up to 90 percent quicker GPU execution for all your adorable design escalated applications and diversions.


Implementing the 510 (K) correctly in compliance with the latest proposed FDA changes

http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900525SEMINAR?bullet-proof-510(k)-Seattle-WA

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).


Medical products need to be validated for Radiation Sterilization

http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900685SEMINAR?validating-radiation-Washington-DC

“Do it right the first time” should be the mantra for medical device manufacturers that plan to make radiation products. Choosing the most functional and radiation resistant materials for their medical device will help them avoid the trouble of going through the post launch cycle of product revisions. To get this right, one simple line of thinking is crucial for medical device manufacturers to inculcate: To “think like a molecule”. This is the basis on which to plan and design around radiation induced changes in the qualities such as color, odor and brittleness that go into the materials. Learning the right method Professionals in the medical devices industry, who work on these aspects will benefit immensely from a two-day seminar on the topic, “Validating Radiation Sterilization for Medical Products”, which is being organized by GlobalCompliancePanel, a highly popular provider of professional trainings for all areas of regulatory compliance. The Director of this seminar, Karl J. Hemmerich, President of Ageless Processing Technologies, who brings over 35 years of experience in medical device product design, development, manufacturing, and sterilization, will offer a range of learning on this topic. Identifying the best suited materials Apart from helping participants identifying the materials that perform best upon radiation, keeping color and odor out of their irradiated products and enhancing product and packaging designs to take advantage of radiation; he will also offer understanding to them on how to avoid the materials that are certain to fail. This seminar, for which medical device professionals can enroll by visiting http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900685SEMINAR?validating-radiation-Washington-DC, has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Understanding optimum sterilization modality Participants will also learn the basis for choosing the optimum sterilization modality based on materials, product design, bioburden, and logistics and understand which modality (Gamma, E-beam, or X-ray) will perform best for their product. Karl will cover the areas relating to validation of radiation sterilization for medical products, such as Materials Guidances - AAMI TIR # 17, ASTM, sterilization validation and bioburden, Shelf Life Test Methods - Accelerated Aging design, Test Design, Product Design, the influences of product assembly (molding, automation, etc.), material selection and post irradiation degradation, Regulatory Guidances - AAMI/ISO 11137, TIR #17, packaging design and materials, and biological polymers - tissue, serum at this two-day in person seminar. The following areas will be covered at this seminar: o Polymers Chemistry - choosing the best polymer candidate o Gamma, E-beam, X-ray sterilization o Accelerated Aging o Product Qualification o Sterilization Validation - Establishing the Minimum Sterilization dose (VDmax) o Sterilization Modality Selection Criteria o Biocompatibility o Preventing Plastic Part Failure Post Irradiation Contact Information: http://www.globalcompliancepanel.com/ +1-800-447-9407


Elements of a Cyber Security Incident Response Program

https://compliance4all14.wordpress.com/2016/09/23/elements-of-a-cyber-security-incident-response-program

A Cyber Security Incident Response Program (CSIRP) or a Cyber Security Incident Response Team (CSIRT) that anticipates and neutralizes a cyber-incident is a critical need for organizations, because an Internet or network security breach results in loss of valuable data, as well as several resources and the organization’s reputation and could potentially invite lawsuits. While putting a CSIRP in place; the management has to take into consideration the fact that Information Security, Governance & Risk, are all critical aspects of planning and execution of the Information Security Plan. It has to decide who in the organization has the key responsibility towards developing an information security governance program. It has to also review existing Information Security policies and standards to gauge their sufficiency vis-à-vis industry best practices, and update them as needed, while meeting the requirements set out by compliance regulations. A webinar to help understand CSIRP The effective ways of doing this will be the focus of a webinar that is being organized by Compliance4All, a highly popular provider of professional trainings for all areas of regulatory compliance. Dr. (Ms.) Michael Redmond, CEO and Lead Consultant for Redmond Worldwide, who served as an Adjunct Professor for Continuity Management at New York University and the Master’s program at John Jay College, will be the speaker at this webinar. More details of this course can be had from http://www.compliance4all.com/control/w_product/~product_id=500961LIVE/ Scope of the training session Ms. Redmond will teach participants of this webinar the ways by which their organizations can put a CSIRP in place. She will help them establish Key Performance Indicators (KPI) to determine if their CSIRP meets business objectives and operational metrics for effecting process improvement. She will also show participating organizations the ways of tailoring and enhancing their existing CSIRP and requirements for specific audiences based on the sensitivity of the information for which they are granted based on policies. Other important learning outcomes offered at this session include how to strengthen IT Risk Management, which involves integrating information security risk management with Enterprise Risk Management and requires using common business terminology, congruent methods, and common or linked risk register, and establishing mechanisms for risk acceptance. Ms. Redmond will also explain to participants how they can build an IS regulation review process, schedule regulation requirements and put in place a set of procedures that help to deal with a breach, malware and related issues.


Tightening carrier food safety issues can save costs for the food and logistics industries

https://compliance4all14.wordpress.com/2016/09/29/tightening-carrier-food-safety-issues-can-save-costs-for-the-food-and-logistics-industries

The fact that between five and eight percent of current recall and shipment rejection issues happen within the cold chain food transportation sector, resulting in fairly high, but preventable financial loss is an indication of how much scope is there to contain seepage in the food and transportation industries. Is this happening because of lack of regulation? No. Rather, it is the lack of proper understanding of these regulations that is at the root of the problem relating to food pilferage. There is no dearth of laws. For instance, there are the Food Safety Modernization Act and the Rules on the Sanitary Transportation of Human and Animal Foods. In addition, for reference, there is also the “guidance” which the FDA previously published, which now has the power of law, being legally enforceable by many government agencies. Complying with these guidances and laws is the way forward for the food and transportation industries. All that is needed is to change mindsets, practices and operations. Inculcating this takes time, and comes about with proper professional training. Ways of implementing the guidances and rules This is what Compliance4All, a leading provider of professional trainings for all the areas of regulatory compliance, will be imparting at a webinar. John Ryan, a Quality Systems professional who has worked for over three decades in a variety of industries globally and owns Ryan Systems, will be the speaker at this webinar. To enroll for this webinar, please visit http://www.compliance4all.com/control/w_product/~product_id=500995 This FDA recommended carrier food safety training course will highlight the problems that may take place in the process of food transportation. John will teach how to implement sound sanitation, temperature monitoring and quality controls, which can go a long way in preventing adulteration during loading, unloading and in-transit operations. Plenty to learn from This course will benefit professionals across the food and food transportation industries, such as Directors and Managers in Food Safety and Quality Personnel, food safety audit teams, perishables logistics personnel, compliance officers, food company CEO's, drivers of food carrying trucks, and food load and unload personnel in a number of ways and help them save avoidable expenses by implementing checks and controls along the food transportation chain. The following areas will be covered at this webinar: o FDA Sanitary and Temperature Controlled FSMA Rules o Definitions: Carrier, Container, Tools and Equipment o Preventive Controls Subpart G: Receiver Liability for Carrier nonconformance o Prevention versus Corrective Action o ATP o GAP Analysis o Pallet versus Case versus Container Temperatures o Temperature Measurement Technologies o Pallet Types o Sanitation Testing o Costs


New Way of Exploring Economic Environment

http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900719SEMINAR?new-economic-environment-Boston-MA

Lineament analysis in geological exploration The existence of efficient and cost-effective methods that help to identify prospective targets that are related to or are influenced by tectonic structures is not common knowledge among professionals in the field of geological exploration. The right sampling and Quality Assurance/Quality Control (QA/QC) procedures are essential in all aspects of the mineral deposit evaluation process to achieve the best possible confidence in resultant mineral resource and reserve estimates. Getting Quality Assurance and Quality Control procedures and protocols right is crucial Accurate and proper QA and QC procedures and protocols are essential to ensure that data collected and created by the mining organization is of a high level of quality and is in compliance with CIM Standards and Guidelines. Geological quality control procedures are meant to monitor precision and accuracy of the assay data, as well as possible sample contamination during sample preparation and assaying. The quality of the data used determines the quality of an estimate. To offer a complete understanding of this concept, GlobalCompliancePanel, a reputable provider of professional trainings for all areas of regulatory compliance, will be organizing a two-day, live seminar. Please visit http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900719SEMINAR?new-economic-environment-Boston-MA. The Director of this seminar, Ricardo Valls, will introduce to the participants a methodology that will help them to concentrate their exploration efforts even over new areas with limited or nonexistent geological information, while keeping their budget in check. The centrality of QA&QC procedures Ricardo will explain how lineament and satellite interpretation are a way to define where to concentrate exploration efforts, as well as how to implement QA&QC procedures to guarantee the quality of the collected data. This is necessary, considering that compliance with the industry-established QA/QC is no longer an option, but a necessity for all the companies to implement, especially those that trade in the markets. Quality assurance is essentially the management system that operates to ensure credible results. The prime objective of the field QA program is to maximize accuracy by reducing introduced variability. The learning will be gleaned from a quality assurance program that the Director has implemented for the field sampling procedures. This includes collection, labeling, and shipping components. The quality control component of this system is a set of activities intended to control the quality of the data from collection through to analysis. It consists of day-to-day activities such as: o The adherence to written protocols; up-to-date and suitable training of personnel o The use of reliable laboratories with excellent QA&QC systems in place o The regular use of quality control (QC) samples (blanks, standard samples, and field duplicates) o Diligent record keeping. Ricardo will cover the following areas at this seminar: o History of the problem, why we need to change the current approach o Lineament analysis o Lineament analysis and satellite interpretation of data o Physical modeling (3D strain analysis and 3D stress analysis) o Statistical procedures (Compositional data analysis, correlation analysis, principal component and other methods) o Defining a QA/QC program, Blanks, duplicates, standards, external controls o Procedures and audits o Rock naming in the field o Conclusions and recommendations.


Emerging Issues in Food Safety-Globally

https://www.linkedin.com/pulse/emerging-issues-food-safety-globally-shahanshah-manzoor?trk=mp-author-card

The Global Food Safety Initiative is a private enterprise by those in the food industry aimed at offering guidance to the food industry for making food chain safer. This industry-driven initiative seeks to provide thought leadership on the various aspects of food and guides the food industry on implementing safety standards along all the points in the food chain. Origins of the Global Food Safety Initiative: The Global Food Safety Initiative was conceived and finessed in the 1990’s and 2000’s in the backdrop of various international food-related crises such as the mad cow disease in the UK, the dioxin affair in Belgium and the 2008 listeriosis outbreak caused by the Canadian company Maple Leaf. These crises triggered a strong desire for collective action by the food industry for taking creative preventive steps that could stall the occurrence of such events in the future. These crises provided the reason for the birth of the Global Food Safety Initiative. The Global Food Safety Initiative was born out of the realization by leaders in the food supply and retail industries of the lack of coordinated audit procedures in the industry. Whatever audit and other checks and balances methods existed till then were largely fragmented, which is why they believed these crises happened. One of the primary aims of the Global Food Safety Initiative was to coalesce these procedures and set standards for their implementation. The Global Food Safety Initiative, which was created out of collaborative actions from an independent network, the Consumer Goods Forum (CGF), which consisted of CEO’s from the leading players of the food retail industry, has a vision of making safe food available to consumers, no matter where they are located. Objectives of the Global Food Safety Initiative: The core objectives of the Global Food Safety Initiative are: The workings of the Global Food Safety Initiative: The Global Food Safety Initiative carries out its aims and objectives by holding meetings, conferences and seminars and other such events at local and regional levels. The aim of the Global Food Safety Initiative is to use these events as the platform for sharing knowledge of how to go about their work. The Directors of the Global Food Safety Initiative are chosen from among the leaders of the industry. The CGF drives the day-to-day functions and administration of the Global Food Safety Initiative. Certification from The Global Food Safety Initiative: Depending on the stream of retail business a company is in, The Global Food Safety Initiative issues certificates to entities that satisfy its conditions on meeting safety standards. To get certified from the Global Food Safety Initiative, companies in the food retail industry need to meet required standards by having the necessary audits carried out for their systems. Once a Global Food Safety Initiative certificate is issued, the organization has to ensure its upkeep by carrying out regular subsequent actions as required.