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  • Evaluating and Investigating Drug Safety Signals with Public Databases Webinar

    - by Roxana Babiciu
    In this one-hour webinar, BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, will review a number of public databases available to use during the evaluation and investigation of identified safety signals. The discussion will focus on the use of free and paid longitudinal healthcare databases available online. After attending this presentation, you will better understand how these data sources can be used in your daily PV work. Read more here

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  • Best commercial libraries for developing NCPDP-based systems (prescription drug related)

    - by Kaveh Shahbazian
    What are (based on experiences) best commercial libraries for developing NCPDP-based systems? Edit 2: Thanks to all for help! NCPDP (National Council for Prescription Drug Programs) is an standard for e-prescribing. It defines two formats for message transmission: binary and XML. Implementing XML is somehow easier because it is a standard format which in turn gives us more tooling options. The binary format has a very big specification and time-consuming to implement. I did not find an open source solution to work with. So I am looking for commercial alternatives. Edit 1: Please guide me; what's wrong with this question?

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  • Find rows that match multiple (two) criteria

    - by Scott Sanders
    I am trying to get a list of items that match on two criteria. DATE PRODUCT CHANNEL DEC 13 Cat Chow DRUG NOV 13 Pupperoni DRUG DEC 13 Meow Mix DRUG DEC 13 Jerky Treats DRUG This is the data from A1 to C5. I want all the product sold on DEC 13 and in the DRUG channel. This is the formula that I have now, which is only bringing back the first example. INDEX($B$2:$B$5, MATCH(1, ("DRUG"=$C$2:$C$5)*("DEC 13"=$A$2:$A$5), 0) )

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  • Can I place AdSense ads on a site with drug content?

    - by Joe Majewski
    I am going to be opening a new WordPress blog today, and I was curious to know if my site will be appropriate for AdSense ads. First off, the blog is going to be about drug addiction. More specifically, opiate addiction. I myself was addicted to pain killers for three years, and I am pleased to say that I am now in treatment and I have not used in over a month now. :) Anyways, my site will be an informative blog about opiates and the harm that they can induce on one's life. It will in no way endorse the use of drugs, but I may talk about my negative experiences. It will be 100% (without a doubt) evident upon checking out my website that my view on drugs is negative. Two questions: (1) Is this content acceptable for Google's terms of service? (2) In order to begin displaying AdSense ads, is there anything I must first do? I already have AdSense ads running on one of my domains. Can I simply begin pasting the code snippets into my new domain and watch as the ads begin to work? Thanks for your time. :)

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  • Control cell reference increment when dragging a forumula in Libre Office Calc (3.5)

    - by Chuck
    Using Libre Office Calc (3.5) and have a question. When copying a formula that references cells into multiple empty cells the default is to increment each cell reference by one column or row, depending on the direction that the formula is being drug. A formula '= 1 + A1' drug horizontally changes to '= 1 + B1' when pulled one cell to right and '=1 + A2' when pulled one cell down. Is there a way to control increase the increment of the referenced cell? Is is possible to have a formula '= 1 + A1' that effectively changes to '= 1 + A3' when drug down one cell, '= 1 + A5' when drug down two cells, etc? If it matters, I am trying to take a constantly updating master list of data that is organized by dates (Wednesdays and Saturdays) and create separate spread sheets for each day of the week that can be updated by only pulling down the formula into the next cell. My attempts at using the 'lookup' function, 'offset' function, and creating a sort column in Libre Office Calc are thwarted by my inability to figure out how to get around the single step increment when pulling a formula down into the next cell. Thanks

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  • Apache2 + Php + Pthreads HowTos

    - by Drug
    04 LTS 64 bit. What I would really love to do is sudo apt-get install libapache2-mod-php5 but compile PHP with --enable-maintainer-zts so I could later install pthreads with pecl install pthreads. Sadly I understand that it is not possible. I know that the easiest way is to recompile PHP together with apache support and zts. However I really like the way the standard Ubuntu PHP package is configured and I am used to the path`s for CLI php.ini config, Apache php.ini config and other paths for modules and files that this Ubuntu package defines. So i just want to change the package source a little bit and install it. # Get the stuff necessary to build the package sudo apt-get build-dep php5-common # Get the package source sudo apt-get source php5-common At this point I am getting sources not for the php5-common package but the whole php5 package. If I would sudo make && make install at this point, would it mean that I am installing a lot of unnecessary stuff? # Add configuration options ./configure --enable-maintainer-zts Does this mean that I am appending a configuration option? Or am I generating a whole new config? Alternative at this point Is there a way of getting the config options that this package defines, so that I can grab a php source from php.net and compile it with $ ./configure --prefix=package_prefix \ // Option 1 from package --enable-embed \ // Option 2 from package --with-regex=php \ // Option 3 from package Continuing the main idea ... Solution 1 # Compile (Not compiling) sudo make && make install Will I be building PHP with EVERYTHING at this point? If I compile like this, I will not be able to remove the mess I made using sudo apt-get purge php5? Solution 2 # ReCompile the package dpkg-buildpackage -rfakeroot -uc -b This does not compile also. Please correct my steps, so I can install everything correctly.

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  • Searchable list of objects in Java

    - by Christian
    I want to create a large (~300,000 entries) List of self defined objects of the class Drug. Every Drug has an ID and I want to be able to search the Drugs in logarithmic time via that ID. What kind of List do I have to use? How do I declare that it should be searchable via the ID?

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  • jQuery sortable: Revert changes if update callback makes an AJAX call that fails?

    - by Seth Petry-Johnson
    I am using the jQuery sortable() feature to re-order a list of items. After an item is drug to a new location, I kick off an AJAX form post to the server to save the new order. How can I undo the sort (e.g. return the drug item to its original position in the list) if I receive an error message from the server? Basically, I only want the re-order to "stick" if the server confirms that the changes were saved.

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  • What makes these two R data frames not identical?

    - by Matt Parker
    UPDATE: I remembered dput() about the time Sharpie mentioned it. It's probably the row names. Back in a moment with an answer. I have two small data frames, this_tx and last_tx. They are, in every way that I can tell, completely identical. this_tx == last_tx results in a frame of identical dimensions, all TRUE. this_tx %in% last_tx, two TRUEs. Inspected visually, clearly identical. But when I call identical(this_tx, last_tx) I get a FALSE. Hilariously, even identical(str(this_tx), str(last_tx)) will return a TRUE. If I set this_tx <- last_tx, I'll get a TRUE. What is going on? I don't have the deepest understanding of R's internal mechanics, but I can't find a single difference between the two data frames. If it's relevant, the two variables in the frames are both factors - same levels, same numeric coding for the levels, both just subsets of the same original data frame. Converting them to character vectors doesn't help. Background (because I wouldn't mind help on this, either): I have records of drug treatments given to patients. Each treatment record essentially specifies a person and a date. A second table has a record for each drug and dose given during a particular treatment (usually, a few drugs are given each treatment). I'm trying to identify contiguous periods during which the person was taking the same combinations of drugs at the same doses. The best plan I've come up with is to check the treatments chronologically. If the combination of drugs and doses for treatment[i] is identical to the combination at treatment[i-1], then treatment[i] is a part of the same phase as treatment[i-1]. Of course, if I can't compare drug/dose combinations, that's right out.

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  • SOA, Governance, and Drugs

    Why is IT governance important in service oriented architecture (SOA)? IT Governance provides a framework for making appropriate decisions based on company guidelines and accepted standards. This framework also outlines each stakeholder’s responsibilities and authority when making important architectural or design decisions. Furthermore, this framework of governance defines parameters and constraints that are used to give context and perspective when making decisions. The use of governance as it applies to SOA ensures that specific design principles and patterns are used when developing and maintaining services. When governance is consistently applied systems the following benefits are achieved according to Anne Thomas Manes in 2010. Governance makes sure that services conform to standard interface patterns, common data modeling practices, and promotes the incorporation of existing system functionality by building on top of other available services across a system. Governance defines development standards based on proven design principles and patterns that promote reuse and composition. Governance provides developers a set of proven design principles, standards and practices that promote the reduction in system based component dependencies.  By following these guidelines, individual components will be easier to maintain. For me personally, I am a fan of IT governance, and feel that it valuable part of any corporate IT department. However, depending on how it is implemented can really affect the value of using IT governance.  Companies need to find a way to ensure that governance does not become extreme in its policies and procedures. I know for me personally, I would really dislike working under a completely totalitarian or laissez-faire version of governance. Developers need to be able to be creative in their designs and too much governance can really impede the design process and prevent the most optimal design from being developed. On the other hand, with no governance enforced, no standards will be followed and accepted design patterns will be ignored. I have personally had to spend a lot of time working on this particular scenario and I have found that the concept of code reuse and composition is almost nonexistent.  Based on this, too much time and money is wasted on redeveloping existing aspects of an application that already exist within the system as a whole. I think moving forward we will see a staggered form of IT governance, regardless if it is for SOA or IT in general.  Depending on the size of a company and the size of its IT department,  I can see IT governance as a layered approach in that the top layer will be defined by enterprise architects that focus on abstract concepts pertaining to high level design, general  guidelines, acceptable best practices, and recommended design patterns.  The next layer will be defined by solution architects or department managers that further expand on abstracted guidelines defined by the enterprise architects. This layer will contain further definitions as to when various design patterns, coding standards, and best practices are to be applied based on the context of the solutions that are being developed by the department. The final layer will be defined by the system designer or a solutions architect assed to a project in that they will define what design patterns will be used in a solution, naming conventions, as well as outline how a system will function based on the best practices defined by the previous layers. This layered approach allows for IT departments to be flexible in that system designers have creative leeway in designing solutions to meet the needs of the business, but they must operate within the confines of the abstracted IT governance guidelines.  A real world example of this can be seen in the United States as it pertains to governance of the people in that the US government defines rules and regulations in the abstract and then the state governments take these guidelines and applies them based on the will of the people in each individual state. Furthermore, the county or city governments are the ones that actually enforce these rules based on how they are interpreted by local community.  To further define my example, the United States government defines that marijuana is illegal. Each individual state has the option to determine this regulation as it wishes in that the state of Florida determines that all uses of the drug are illegal, but the state of California legally allows the use of marijuana for medicinal purposes only. Based on these accepted practices each local government enforces these rules in that a police officer will arrest anyone in the state of Florida for having this drug on them if they walk down the street, but in California if a person has a medical prescription for the drug they will not get arrested.  REFERENCESThomas Manes, Anne. (2010). Understanding SOA Governance: http://www.soamag.com/I40/0610-2.php

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  • Website Editor control for WYSIWYG/regions

    - by Dan Smith
    For lack of a better title, let me try to explain further: I'm looking for a control that will allow me to have a library of "page elements" (such as a list of employees, or a photo gallery, or a contact form, etc) that could be dragged onto the page canvas. The page canvas could have pre-set regions/boxes where these items could be drug into, preventing the user from screwing up the pages layout. I'm looking for any pre-built commercial (or open-source with commercial use allowed) tools available like this.

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  • What effects do various drugs have on coding style / productivity? [closed]

    - by codecraft
    Can anyone tell me what the effect of various drugs are on coding style, and if coding on drugs can be more productive, or more fun? Are some types of drugs better suited to certain tasks and phases of software development? And which programming languages are best suited to coding on drugs? It would be great if you could back up your answers by data, probably even code snippets showcasing the effect of the drug experience.

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  • Unlocking Productivity

    - by Michael Snow
    Unlocking Productivity in Life Sciences with Consolidated Content Management by Joe Golemba, Vice President, Product Management, Oracle WebCenter As life sciences organizations look to become more operationally efficient, the ability to effectively leverage information is a competitive advantage. Whether data mining at the drug discovery phase or prepping the sales team before a product launch, content management can play a key role in developing, organizing, and disseminating vital information. The goal of content management is relatively straightforward: put the information that people need where they can find it. A number of issues can complicate this; information sits in many different systems, each of those systems has its own security, and the information in those systems exists in many different formats. Identifying and extracting pertinent information from mountains of farflung data is no simple job, but the alternative—wasted effort or even regulatory compliance issues—is worse. An integrated information architecture can enable health sciences organizations to make better decisions, accelerate clinical operations, and be more competitive. Unstructured data matters Often when we think of drug development data, we think of structured data that fits neatly into one or more research databases. But structured data is often directly supported by unstructured data such as experimental protocols, reaction conditions, lot numbers, run times, analyses, and research notes. As life sciences companies seek integrated views of data, they are typically finding diverse islands of data that seemingly have no relationship to other data in the organization. Information like sales reports or call center reports can be locked into siloed systems, and unavailable to the discovery process. Additionally, in the increasingly networked clinical environment, Web pages, instant messages, videos, scientific imaging, sales and marketing data, collaborative workspaces, and predictive modeling data are likely to be present within an organization, and each source potentially possesses information that can help to better inform specific efforts. Historically, content management solutions that had 21CFR Part 11 capabilities—electronic records and signatures—were focused mainly on content-enabling manufacturing-related processes. Today, life sciences companies have many standalone repositories, requiring different skills, service level agreements, and vendor support costs to manage them. With the amount of content doubling every three to six months, companies have recognized the need to manage unstructured content from the beginning, in order to increase employee productivity and operational efficiency. Using scalable and secure enterprise content management (ECM) solutions, organizations can better manage their unstructured content. These solutions can also be integrated with enterprise resource planning (ERP) systems or research systems, making content available immediately, in the context of the application and within the flow of the employee’s typical business activity. Administrative safeguards—such as content de-duplication—can also be applied within ECM systems, so documents are never recreated, eliminating redundant efforts, ensuring one source of truth, and maintaining content standards in the organization. Putting it in context Consolidating structured and unstructured information in a single system can greatly simplify access to relevant information when it is needed through contextual search. Using contextual filters, results can include therapeutic area, position in the value chain, semantic commonalities, technology-specific factors, specific researchers involved, or potential business impact. The use of taxonomies is essential to organizing information and enabling contextual searches. Taxonomy solutions are composed of a hierarchical tree that defines the relationship between different life science terms. When overlaid with additional indexing related to research and/or business processes, it becomes possible to effectively narrow down the amount of data that is returned during searches, as well as prioritize results based on specific criteria and/or prior search history. Thus, search results are more accurate and relevant to an employee’s day-to-day work. For example, a search for the word "tissue" by a lab researcher would return significantly different results than a search for the same word performed by someone in procurement. Of course, diverse data repositories, combined with the immense amounts of data present in an organization, necessitate that the data elements be regularly indexed and cached beforehand to enable reasonable search response times. In its simplest form, indexing of a single, consolidated data warehouse can be expected to be a relatively straightforward effort. However, organizations require the ability to index multiple data repositories, enabling a single search to reference multiple data sources and provide an integrated results listing. Security and compliance Beyond yielding efficiencies and supporting new insight, an enterprise search environment can support important security considerations as well as compliance initiatives. For example, the systems enable organizations to retain the relevance and the security of the indexed systems, so users can only see the results to which they are granted access. This is especially important as life sciences companies are working in an increasingly networked environment and need to provide secure, role-based access to information across multiple partners. Although not officially required by the 21 CFR Part 11 regulation, the U.S. Food and Drug Administraiton has begun to extend the type of content considered when performing relevant audits and discoveries. Having an ECM infrastructure that provides centralized management of all content enterprise-wide—with the ability to consistently apply records and retention policies along with the appropriate controls, validations, audit trails, and electronic signatures—is becoming increasingly critical for life sciences companies. Making the move Creating an enterprise-wide ECM environment requires moving large amounts of content into a single enterprise repository, a daunting and risk-laden initiative. The first key is to focus on data taxonomy, allowing content to be mapped across systems. The second is to take advantage new tools which can dramatically speed and reduce the cost of the data migration process through automation. Additional content need not be frozen while it is migrated, enabling productivity throughout the process. The ability to effectively leverage information into success has been gaining importance in the life sciences industry for years. The rapid adoption of enterprise content management, both in operational processes as well as in scientific management, are clear indicators that the companies are looking to use all available data to be better informed, improve decision making, minimize risk, and increase time to market, to maintain profitability and be more competitive. As more and more varieties and sources of information are brought under the strategic management umbrella, the ability to divine knowledge from the vast pool of information is increasingly difficult. Simple search engines and basic content management are increasingly unable to effectively extract the right information from the mountains of data available. By bringing these tools into context and integrating them with business processes and applications, we can effectively focus on the right decisions that make our organizations more profitable. More Information Oracle will be exhibiting at DIA 2012 in Philadelphia on June 25-27. Stop by our booth Normal 0 false false false EN-US X-NONE X-NONE MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;} (#2825) to learn more about the advantages of a centralized ECM strategy and see the Oracle WebCenter Content solution, our 21 CFR Part 11 compliant content management platform.

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  • Finding a Payment Gateway?

    - by Lynda
    I have a client who would like to sell glass pipes online. The problem I run into is with the payment gateway. Glass pipes fall into two categories drug paraphernalia or tobacco product. This leads me to here and asking: Does anyone know of a payment gateway that will process payments for glass pipes? Note: Doing some Google searching I read that Authorize.net will accept tobacco but when I spoke with them they said they do not.

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  • Many-to-many relationships in pharmacology

    - by John Paul Cook
    When I was in my pharmacology class this morning, I realized that the instructor was presenting a classic relational database management system problem: the many-to-many relationship. He said that all of us in nursing school must know our drugs backwards and forwards. I know how to model that! There are so many things in both healthcare and higher education that could benefit from an appropriate application of technology. As a student, I'd like to be able to start with a drug, a disease, a name of...(read more)

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  • Protect Your Brand with Oracle Pedigree and Serialization Manager in R12.1.3

    The pharmaceutical industry is facing new challenges as counterfeit products enter the ethical drug supply chain. Companies need to better secure the movement of their branded products from manufacturing to distribution to the end customer to insure proper efficacy. Pharmaceuticals are of special targets to "knock-offs", non-authorized generics as pirated-products enter the market. Oracle Pedigree and Serialization Manager (OPSM) helps firms' better track and control their products through a unique monitoring process.

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  • Libraries for developing NCPDP SCRIPT based systems (a standard for e-prescribing)

    - by Kaveh Shahbazian
    What are (based on experiences) best (commercial or open source) libraries for developing NCPDP-based systems? Background: NCPDP (National Council for Prescription Drug Programs) is a not-for-profit, ANSI-accredited, standards development organization. One of it's standards is the SCRIPT Standard for Electronic Prescribing, which allows PHARMACY, PRESCRIBER (i.e. Physician) and PAYERS (patient or more often insurer) communicate. So the SCRIPT standard is about data transmission. Problem: One step in implementing such systems is to develop models for data based on SCRIPT standard. These models should have utilities for serializing/deserializing to/from SCRIPT binary format and SCRIPT XML format (there are two distinct formats here; both must be supported). Here rises the problem (for me at least). To develop this subsystem for handling the model, implementing serializing and deserializing facilities and keep it uptodate with the SCRIPT standard specifications is a lot of work; it needs it's own team and team management issues (to support a standard implementation). So I am looking for a solution to this problem; to keep standard implementation out of the way and focusing on main problems. Thanks to all (Thankyou Freiheit for your hints!) Edit 2: Thanks to all for help! NCPDP (National Council for Prescription Drug Programs) is an standard for e-prescribing. It defines two formats for message transmission: binary and XML. Implementing XML is somehow easier because it is a standard format which in turn gives us more tooling options. The binary format has a very big specification and time-consuming to implement. I did not find an open source solution to work with. So I am looking for commercial alternatives. Edit 1: Please guide me; what's wrong with this question?

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  • How can i programmatically use aero snap features from C# code

    - by user1739957
    I have a simple question. How can I access aero snap programmatically from my C# code. Like, if I click a button "Snap Left", I want my program window to snap to the left, just like when its drug over there manually. I looked all over SO, but all the questions seem to be about aero snap not working with a form, and keeping it from snapping a form. Not programmatically snapping a form. I'm happy to use interloping. Thanks

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  • redoing object model construction to fit with asynchronous data fetching

    - by Andrew Patterson
    I have a modeled a set of objects that correspond with some real world concepts. TradeDrug, GenericDrug, TradePackage, DrugForm Underlying the simple object model I am trying to provide is a complex medical terminology that uses numeric codes to represent relationships and concepts, all accessible via a REST service - I am trying to hide away some of that complexity with an object wrapper. To give a concrete example I can call TradeDrug d = Searcher.FindTradeDrug("Zoloft") or TradeDrug d = new TradeDrug(34) where 34 might be the code for Zoloft. This will consult a remote server to find out some details about Zoloft. I might then call GenericDrug generic = d.EquivalentGeneric() System.Out.WriteLine(generic.ActiveIngredient().Name) in order to get back the generic drug sertraline as an object (again via a background REST call to the remote server that has all these drug details), and then perhaps find its ingredient. This model works fine and is being used in some applications that involve data processing. Recently however I wanted to do a silverlight application that used and displayed these objects. The silverlight environment only allows asynchronous REST/web service calls. I have no problems with how to make the asychhronous calls - but I am having trouble with what the design should be for my object construction. Currently the constructors for my objects do some REST calls sychronously. public TradeDrug(int code) { form = restclient.FetchForm(code) name = restclient.FetchName(code) etc.. } If I have to use async 'events' or 'actions' in order to use the Silverlight web client (I know silverlight can be forced to be a synchronous client but I am interested in asychronous approaches), does anyone have an guidance or best practice for how to structure my objects. I can pass in an action callback to the constructor public TradeDrug(int code, Action<TradeDrug> constructCompleted) { } but this then allows the user to have a TradeDrug object instance before what I want to construct is actually finished. It also doesn't support an 'event' async pattern because the object doesn't exist to add the event to until it is constructed. Extending that approach might be a factory object that itself has an asynchronous interface to objects factory.GetTradeDrugAsync(code, completedaction) or with a GetTradeDrugCompleted event? Does anyone have any recommendations?

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  • List of drugs for sample data

    - by Skoder
    Where can I find a list of common medical drugs? Researching and typing 150+ drug names would be quite inefficient. In general, are there any sites which have a list of items for developers to use in applications? For example, you can download dictionaries in specific formats (e.g. XML) for use in word games.

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  • How to use JSON response in the form of JSTL?

    - by HariKrishna
    I am getting JSON response,now i need to construct a table using this response.The table may be contain more than one record and i know one way of doing this is using Jstl tags but not JSON response.Here is my jsp code <div id="divHideAllergies" class="clone"> <div class="copy"> <div class="col-md-12"> <div class="portlet box carrot "> <div class="portlet-title"> <div class="caption"> <i class="fa fa-medkit"></i> Allergies </div> </div> <div class="portlet-body form"> <div class="form-body"> <div class="form-group"> <label class="control-label col-md-3">Allergy Type:</label> <div class="col-md-9"> <div class="input-group"> <span class="input-group-addon"><i class="fa fa-medkit"></i></span> <select class="form-control" id="allergy_type"> <option selected value="">--Select One--</option> <option value="Drug">Drug</option> <option value="Environmental">Environmental</option <option value="Food">Food</option> </select> </div> </div> </div> <div class="form-group"> <label class="control-label col-md-3">Allergic to:</label> <div class="col-md-9"> <div class="input-group"> <span class="input-group-addon"><i class="fa fa-medkit"></i></span> <input type="text" class="form-control" name="first name" id="allergy_to"/> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div>

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  • Why is IaaS important in Azure&hellip;

    - by Steve Loethen
    Three weeks ago, Microsoft released the next phase of Azure.  I have had several clients waiting on this release.  The fact that they have been waiting and are now more receptive to looking at the cloud.  Customers expressed fear of the unknown.  And a fear of lack of control, even when that lack of control also means a huge degree of flexibility to innovate with concerns about the underlying infrastructure.  I think IaaS will be that “gateway drug” to get customers who have been hesitant to take another look at the cloud.  The dialog can change from the cloud being this big scary unknown to a resource for workloads.  The conversations should have always been, and can know be even stronger, geared toward the following points: 1) The cloud is not unicorns and glitter, the cloud is resources.  Compute, storage, db’s, services bus, cache…..  Like many of the resources we have on-premise.  Not magic, just another resource with advantages and obstacles like any other resource. 2) The cloud should be part of the conversation for any new project.  All of the same criteria should be applied, on-premise or off.  Cost, security, reliability, scalability, speed to deploy, cost of licenses, need to customize image, complex workloads.  We have been having these discussions for years when we talk about on-premise projects.  We make decisions on OS’s, Databases, ESB’s, configuration and products based on a myriad of factors.  We use the same factors but now we have a additional set of resources to consider in our process. 3) The cloud is a great solution looking for some interesting problems.  It is our job to recognize the right problems that fit into the cloud, weigh the factors and decide what to do. IaaS makes this discussion easier, offers more choices, and often choices that many enterprises will find more better than PaaS.  Looking forward to helping clients realize the power of the cloud.

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  • Booby Traps and Locked-in Kids: An Interview with a Safecracker

    - by Jason Fitzpatrick
    While most of our articles focus on security of the digital sort, this interview with a professional safecracker is an interesting look the physical side of securing your goods. As part of their Interviews with People Who Have Interesting or Unusual Jobs series over at McSweeney’s, they interviewed Ken Doyle, a professional a locksmithing and safecracking veteran with 30 years of industry experience. The interview is both entertaining and an interesting read. One of the more unusual aspects of safecracking he highlights: Q: Do you ever look inside? A: I NEVER look. It’s none of my business. Involving yourself in people’s private affairs can lead to being subpoenaed in a lawsuit or criminal trial. Besides, I’d prefer not knowing about a client’s drug stash, personal porn, or belly button lint collection. When I’m done I gather my tools and walk to the truck to write my invoice. Sometimes I’m out of the room before they open it. I don’t want to be nearby if there is a booby trap. Q: Why would there be a booby trap? A: The safe owner intentionally uses trip mechanisms, explosives or tear gas devices to “deter” unauthorized entry into his safe. It’s pretty stupid because I have yet to see any signs warning a would-be culprit about the danger. HTG Explains: Why Linux Doesn’t Need Defragmenting How to Convert News Feeds to Ebooks with Calibre How To Customize Your Wallpaper with Google Image Searches, RSS Feeds, and More

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  • Get to Know a Candidate (5 of 25): Jim Carlson&ndash;Grassroots Party

    - by Brian Lanham
    DISCLAIMER: This is not a post about “Romney” or “Obama”. This is not a post for whom I am voting. Information sourced for Wikipedia. Carlson is an American businessman and the Grassroots Party nominee. Carlson is the owner of Last Place on Earth, a head shop located in Duluth, Minnesota. In September 2011, the shop was raided by police for selling bath salts and synthetic marijuana. After the raid, Carlson filed a lawsuit to strike down Minnesota's ban on the substances. His suit was dismissed by the court in November 2011. The Grassroots Party was created in the 1980s to oppose drug prohibition.  The party shares many of the the political leftist values of the Green Party but with a greater emphasis on marijuana/hemp legalization issues.  The permanent platform of the Grassroots Party is the Bill of Rights. Individual candidate's positions on issues vary from Libertarian to Green. All Grassroots candidates would end marijuana/hemp prohibition and re-legalize Cannabis for all its uses. Learn more about Jim Carlson and Grassroots Party on Wikipedia.

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