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![]() Everything] House of Targaryen Complete Family Tree : gameofthrones. For one, there are appendices in the backs of the books, one of which has a summary of all the Targaryen kings. The Worldbook goes through a lot of history. Also, why does the tree go back so far when 9. ![]() The first person on the tree was the first King of the Seven Kingdoms, Aegon the Conquerer, who landed with his free dragons and united Westeros. He founded the Targaryen Dynasty, so the logical place for the tree to start is there. Besides, it's remarkable how many of these people are still relevant: the third king, Maegor the Cruel was the one who abolished the Faith Militant, which was just brought back by Cersei. Aegon II started the Dance of Dragons, which ended in the extinction of dragons, until Daenerys brought them back. Daeron I conquered Dorne, bringing it into the realm for the first time. Baelor the Blessed built the Sept of Baelor, which has been an important backdrop for many major events in the story of Game of Thrones, and then he brought Dorne back into the Seven Kingdoms by a marriage pact. This is the British monarchs' family tree. Simplified English and British monarchs family tree. Key - The red border indicates the monarchs. and children.
Best 2. 5+ Victoria family tree ideas on Pinterest. Red King Family Tree. Edit. despite being unendowed were known to be descendents of the Red King by both families possibly. Charlie Bone Wiki is a.D Pharmacotherapeutics is the study of the use of drugs to diagnose, treat, and prevent conditions. Clinical pharmacology is concerned with all aspects of drug-human.![]() · What are the most commonly prescribed opioids? Hydrocodone: The main ingredient in drugs such as Vicodin and Lortab, hydrocodone comes in various forms. The US Food and Drug Administration (FDA) is broadly charged with ensuring food, drug, device, and cosmetic safety for products marketed and sold in the United States. Note: Press announcements from 2004 to 2014 are available through the FDA.gov Archive. Some links in press announcements may no longer be active. Mylan - Wikipedia. Mylan N. V. is an American global generic and specialty pharmaceuticals company registered in the Netherlands, with principal executive offices in Hatfield, Hertfordshire, UK and global headquarters in Canonsburg, Pennsylvania, US.[2] In 2. Mylan acquired a controlling interest in India- based Matrix Laboratories Limited, a top producer of active pharmaceutical ingredients (APIs) for generic drugs,[3] and the generics business of Germany- based Merck KGa. A.[4] Through these acquisitions, Mylan grew from the third- largest generic and pharmaceuticals company in the United States to the second- largest generic and specialty pharmaceuticals company in the world.[5]In 2. Mylan's pricing of the Epi. Pen, an epinephrine autoinjector, became controversial and was widely referred to as "price gouging". As a result, investigations were opened into whether Mylan had misclassified the Epi. ![]() Pen under the Medicaid Drug Rebate Program, a common form of pharmaceutical fraud. In October 2. 01. Mylan settled these investigations with the U. S. Department of Justice, agreeing to pay $4. In a report published on June 1. Institutional Shareholder Services criticized Mylan for the "outsized compensation" of Mylan's directors. Former CEO Robert Coury received a "$9. Epi. Pen controversies" and "steep shareholder losses." The report urged Mylan's shareholders to "oust all of Mylan's existing directors".[6]Operations[edit]Mylan Inc. In North America and South America, Mylan operates: Mylan Pharmaceuticals, based in Morgantown, West Virginia. Mylan Pharmaceuticals ULC (Mylan Canada)Mylan Technologies Inc. MTI) - transdermal drug delivery systems (TDDS) and related technologies[7]UDL Laboratories Inc. Somerset Pharmaceuticals Inc. Tampa, Florida, owned by Mylan. Somerset develops Emsam, manufactured by Mylan Technologies and marketed in the United States by Dey, another Mylan company[8][9]Mylan Laboratories Limited, Campos dos Goytacazes, Brazil. In Oceania and Central, East, South, and Southeast Asia, Mylan operates: [1. In Europe, Africa, and West Asia, Mylan operates: [1. Operates under the Mylan name in Austria, Belgium, the Czech Republic, Denmark, Finland, France, Germany, Hungary, Italy, the Netherlands, Norway, Poland, Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland, the United Kingdom. Also operates in South Africa. Arcana Arzneimittel Gmb. H - Germany[1. 2]Generics Pharma Hellas - Greece[1. Gerard Laboratories - Ireland[1. Qualimed - trademark in France, but will stop being marketed under the brand name[1. Docpharma - generic pharmaceutical distribution company in Belgium, the Netherlands and Luxembourg. Location[edit]Founded in 1. White Sulphur Springs, West Virginia.[1. The company moved to Morgantown, West Virginia, in 1. Pittsburgh suburb Canonsburg, Pennsylvania. Finally in 2. 00. Southpointe, a suburban business park located in Cecil Township, where it is still located.[1. On February 2. 3, 1. Mylan had its initial public offering (IPO),[1. OTC market under the ticker symbol MYLN. In 1. 97. 6 the stock moved to NASDAQ. Their final stock move was in 1. New York Stock Exchange under the ticker symbol MYL. Currently, the stock is traded on the NASDAQ. History[edit]Mylan Pharmaceuticals was founded as a drug distributor in 1. Milan Puskar and Don Panoz.[1. In 1. 96. 6 Mylan began manufacturing penicillin G tablets as well as vitamins and other dietary supplements.[1. Panoz left Mylan in 1. Puskar quit the company in 1. Roy Mc. Knight as board chairman, who convinced Puskar to return in 1. Mylan discontinued operating as a contract manufacturing organization in 1. Mylan- labeled" brand.[citation needed]With the passage of the Hatch- Waxman Act in 1. Mylan and other small generic companies gained value; in the eighteen months following passage of the law Mylan's earnings grew 1. In the 1. 98. 0s one of the most prescribed drugs in the US was Dyazide, a diuretic that was a combination drug containing triamterene and hydrochlorothiazide; it had been on the market since 1. Complications arose with the introductions of generics versions, because the formulation of Dyazide resulted in variable batches that made it impossible for generic manufacturers to show that their versions were bioequivalent.[2. Some generic companies committed fraud trying to bring a generic version of Dyazide. Bolar Pharmaceutical had the first generic version approved in 1. Bolar had fraudulently substituted Dyazide for its own version to conduct studies that were submitted to the FDA. By 1. 98. 9 the FDA rescinded its approval based on its suspicions and filed criminal charges against Bolar, to which Bolar eventually pled guilty in 1. Mylan chose to develop a new version of a triamterene/hydrochlorothiazide combination drug instead of going the generic route; it developed a different, more stable formulation[2. Dyazide's 2. 5 mg hydrochlorothiazide and 5. This drug had to get approval as a new drug, as opposed to a generic; their product was called Maxzide and was approved in 1. The higher dose allowed once per day dosing, which Mylan and its marketing partner, Lederle, believed would help it compete against Dyazide, which had $2. M in sales in 1. 98. However, Mylan's patents on the drug were declared invalid in court, and its marketing exclusivity expired in 1. Mylan had concerns about the practices of its competitors and the FDA in general, and also with regard to companies seeking to bring generic versions of Maxzide. Mylan hired private investigators to examine its competitors' practices, and when it found evidence of corruption, it submitted it to the House Oversight and Investigations Committee, which investigated and found fraud and corruption within the Food and Drug Administration's generic drugs division and at other generic companies.[1. Two of the companies that had gotten approval to market generic versions of Maxzide, Vitarine Pharmaceutical and Par Pharmaceutical, were targets of Mylan's initial investigation and were found to have used Mylan's Maxzide to obtain their bioequivalence data, leading both companies to withdraw its generic competitor to Mylan's product.[1. The corruption in the nascent generics industry and at the office in the FDA regulating it was widely covered in the media, and led to widespread concern among doctors and the public in the late 1. In 1. 98. 7 Mylan agreed to enter into a joint venture with Bolar to buy Somerset Pharmaceuticals; Mylan wanted access to Somersets' drug discovery capabilities as well as its new drug for Parkinson's, selegiline; the deal was completed in 1. FDA approval of selegiline, which came in 1. Mylan acquired Bertek Inc. Mylan renamed the company Mylan Technologies Inc. MTI).[3. 4] MTI eventually came to be the contract manufacturer for the selegiline transdermal patch and was the first company to market generic nitroglycerin, estradiol, clonidine, and fentanyl transdermal patches.[3. Mylan acquired UDL Laboratories, a supplier of unit dose generic medications to institutional and long- term care facilities in 1. In 1. 99. 8 when it was the world's second largest generics company, Mylan came under investigation from the Federal Trade Commission after it raised the prices of its products, tripling them in the case of lorazepam; Mylan had entered into an exclusive agreement with Profarmica, an Italian company that supplied drug ingredients, after which Mylan's competitors had higher prices and a diminished supply of raw ingredients for lorazepam and other drugs.[3. Before the round of price increases the price of generic drugs had been 5 - 1. The FTC filed suit at the end of 1. Mylan paying a total of $1. M - - $1. 00. M in disgorged profits into a fund to reimburse consumers and state agencies that had overpaid, $8 million in attorney's fees to the State Attorneys General, $3. Mylan and three ingredient suppliers (Cambrex Corporation, Profarmaco S. R. L., and Gyma Laboratories) also agreed to an injunction barring them from entering into similar anticompetitive agreements in the future.[3. In 2. 00. 4 Mylan and King Pharmaceuticals began discussing a deal in which Mylan would acquire King for about $4. B; Mylan wanted to expand its presence in branded pharmaceuticals and to acquire King's sales force.[3. The deal became one of the business soap operas of the year, and included an SEC investigation into King's accounting and Carl Icahn obtaining a 9. Mylan and becoming its largest stakeholder in order to kill the deal; the parties called off the deal in February 2. Black Box FDA Warnings and Legal Implications. Ehrenpreis ED, Deepak P, Sifuentes H, Devi R, Du H, Leikin JB. The metoclopramide black box warning for tardive dyskinesia: effect on clinical practice, adverse event reporting, and prescription drug lawsuits. Am J Gastroenterol. Pub. Med. Cross. Ref. Express Helpline- Get answer of your question fast from real experts. Today's Stock Market News and Analysis. CLOSEXPlease confirm your selection. 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![]() ![]() ![]() ![]() How to buy or sell used Adobe software on e. Bay. March 2. 4, 2. Buying and selling used software on e. Bay can often be a hit or miss experience, particularly when dealing with Adobe Systems Incorporated products such as Photoshop, Illustrator and In. Design, or any of their Creative Suite collections. A quick review of. Bay listings for Adobe products returns almost 2,5. When purchased new, these high end graphics and web design programs can cost into the thousands of dollars, so used versions of these programs are obviously highly desirable to buyers in the secondary market. Terry White debunks the top 5 myths about Adobe Creative Cloud. · Does anybody know how Acrobat's e-licence works? The serial # gets stored on the adobe licensing server upon the order/customer id activation? Yes - I. ![]() However, it is no longer enough for a seller to simply deactivate a product from their computer and then provide the Adobe product serial number and installation discs to a buyer. Adobe has a specific set of conditions that must be met by the current owner/seller of the software in order for the product to be registered and activated by a new owner/buyer. First, simply uninstalling an Adobe software product does NOT automatically deactivate it. It MUST be deactivated by using the Help menu (Help > Deactivate) on the computer the product is installed on. Second, Adobe's License Transfer Policy now requires sellers to fill out a Transfer of License application (available on the company's website), where the seller must provide the product name, platform and serial number, along with the seller's name, address, email, signature and a case number the seller must obtain first from Adobe Customer Service. The form also requires the same information from the buyer, as well as a scan of your photo ID, and your proof of purchase (if you didn't purchase directly from Adobe). The completed form must then be submitted by fax to Adobe Customer Service for verification and approval. The dim glow of an e-cigarette activating has become the butt of quite a few jokes about the concept of “cool.” While they’re not hip, the tech behind them is. Choose your region. Selecting a region changes the language and/or content on Adobe.com. After Adobe receives the completed Transfer of License form, Adobe registers the software to the new owner. Registration ensures that Adobe recognizes the new owner as the legal licensee who can receive customer service and support. Adobe's site states it may take three to four weeks for your license transfer request to be processed. In conclusion, if you are looking to buy used Adobe software on e. Bay, ALWAYS ask sellers if they are able to provide a Transfer of License form with the product they are selling, if they do not state it in their auction description. If they cannot (or will not), it is definitely in the buyer's best interest to find a seller that can (and fortunately, many do state upfront that they can provide a TOL). While you may have to wait up to four weeks from Adobe to officially approve the transfer, it may save you the headache of pursuing an e. Bay Buyer Protection case to obtain a refund on your purchase. Delphi 2. 01. 0 code completion not working properly. My code completion in Delphi 2. For example, I put a button on my VCL form, name it "test. BT" and double click on it to add the On. Click event callback. Then I start entering code "test. B" and hit Ctrl- SPACE but the code completion doesn't kick in although it should offer me my button. When I enter "test. BT." and hit Ctrl- SPACE the code completion kicks in and offers me everything for my button. So, code completion works only after the "." It doesn't work for local variables either. Only if they are classes and I enter the variable name including the ".". Any idea what is wrong there? It used to work. Regards,Dirk. Need an online school directory app solution? DirectorySpot's software allows you to easily create a directory app & access it from anywhere. Learn more! Import Export Data, Export Import shipment data from Customs. GOVERNMENT OF INDIAMINISTRY OF FINANCE(DEPARTMENT OF REVENUE)New Delhi, dated the 1. March, 2. 01. 2Notification No. Customs. G. S. R. E).- In exercise of the powers conferred by sub- section (1) of section. Customs Act, 1. 96. Government of India in the Ministry of Finance ( Department of Revenue). No. 2. 1/2. 00. 2- Customs, dated the 1st March, 2. Published in the Gazette of India. Extraordinary, Part II, Section 3, Sub- section (i), vide number G. S. R. 1. 18(E) dated. The Active Directory is supposed to make it easy to control users and groups, but managing it can be difficult. The tools on this page are for the administrator to use.March, 2. 00. 2, except as respects things done or omitted to be done before. Central Government, being satisfied that it is necessary. Table below or column (3) of the said Table read with the relevant. List appended hereto, as the case may be, and falling within the Chapter, heading. First Schedule to the Customs Tariff Act, 1. ![]() Table, when imported into India,- (a) from so much of the duty of customs leviable thereon under the said First. Schedule as is in excess of the amount calculated at the standard rate specified. Table; (b) from so much of the additional duty leviable thereon under sub- section (1). Customs Tariff Act 1. Table, subject to any of the conditions, specified in the Annexure to this. Table: Table. Table S. No. Chapter or Heading or sub–heading or tariff item Description of goods Standard rate Additional duty rate Condition No. Animals and birds imported by zoo Nil - - 2. Cows, heifers, bulls, goats, sheep, pigs, angora rabbits, ducklings and. Grand parent poultry stock and donkey stallions 2. Atlantic salmon 1. Tuna bait Nil - - 6. Live SPFL. vannamei broodstock 1. Goods upto an aggregate of fifty thousand metric tonnes of total imports. Nil - 1 8. 0. 40. Butter, ghee and butter oil 3. White butter, butter oil, anhydrous milk fat upto an aggregate of fifteen. Nil - 1 1. 0. 0. 40. All goods 3. 0% - - 1. ![]() Pancreas 5% - - 1. Conch shell 5% - - 1. All goods Nil - - 1. Artemia cyst, including wet artemia cyst 5% - - 1. Artemia 5% - - 1. Chapter The following goods, namely: - (1) Frozen semen; (2) Frozen semen equipment, namely: - (a) flasks, refrigerators, vessels, jars or dewars, and their accessories. Plastic insemination sheath and insemination guns; and (c) Weaton ampoules and straws for freezing semen 5% - - 1. Planting materials, namely, oil seeds, seeds of vegetables, flowers and. All goods 5% - - 1. All goods Nil - - 2. Pulses 1. 0% - - 2. Pulses Nil - - 2. Powershell – Create Multiple Users in Active Directory Quickly 1. Information. Objective: Simplify the creation of multiple users in Active Directory. Eisenberk https://stackoverflow.com/users/8626725 2017-09-18T13:29:00Z 2017-09-18T13:31:01Z <p>I just started bash and i am doing a search script that search for. Cashew nuts in shell Nil - - 2. All goods Rs. 6. 5/- per kg. All goods 1. 0% - - 2. All goods (excluding areca nuts also known as betel nuts) 3. All goods 2. 0% - - 2. All goods 3. 0% - - 2. All goods 1. 00% - - 2. Sun dried dark seedless raisin 3. All goods, other than black, white or red currants and gooseberries. Long pepper (Piper longum) 3. All goods 3. 5% - - 3. All goods other than meslin 5. Wheat Nil - - 3. 5. Meslin Nil - - 3. All goods 5. 0% - - 3. Goods upto an aggregate of five lakh metric tonnes of total imports of. Nil - 1 3. 8. 1. 00. All goods other than those specified against S. No. 3. 75. 0% - - 3. All goods 3. 0% - - 4. All goods 2. 0% - - 4. All goods (other than those falling under sub- headings 1. All goods 5% - - 4. All goods (other than liquorice roots) 1. Seed lac 5% - - 4. Asafoetida 2. 0% - - 4. All goods 2. 0% - - 4. Oleopine resin 5% - - 4. All goods (other than vegetable seeds and extracts of pyrethrum or of. Bamboo for use in the manufacture of agarbatti 1. Edible oils falling under headings 1. I. The following goods, other than of edible grade, namely: - (A) Crude palm stearin having Free Fatty Acid (FFA) 2. B) All goods (except crude palm oil and crude palm stearin) having Free. Fatty Acid (FFA) 2. C) All goods (except crude palm oil), having Free Fatty Acid (FFA) 2. D) All goods (except crude palm oil), having Free Fatty Acid (FFA) 2. II. The following goods, of edible grade namely,- (A) Crude palm oil falling under heading 1. Nil - 5 (B) Crude Palmolein falling under heading 1. C) Fractions of crude palm oil (other than crude palmolein) falling. Explanation.- For the purposes of this entry, "Crude palm oil". If obtained by extraction an oil shall continue. Nil Nil - - 5 - 5. Refined vegetable oils of edible grade, in loose or bulk form (other. Vegetable oils of edible grade, in loose or bulk form (other than those. S. No. 5. 2 and those falling under heading 1. Vanaspati" or for refining. Explanation.- The expression "Vegetable oil" means- (a) in the case of cottonseed oil, oil having a free fatty acid content. All goods 1. 5% - - 5. All goods Nil - - 5. All goods 7. 5% - - 5. All goods, crude and edible grade Nil - - 5. All goods, refined and edible grade 7. All goods 7. 5% - - 6. Crude sunflower seed or safflower oil upto an aggregate of one lakh and. All goods other than those specified against S. No. 6. 0 7. 5% - - 6. All goods Nil - - 6. All goods 7. 5% - - 6. Refined rape, colza or mustard oil upto an aggregate of one lakh and. All goods, edible grade Nil - - 6. All goods, edible grade 7. All goods 3. 0% - - 6. All goods 8. 0% _ _ 6. All goods, edible grade 7. All goods of edible grade 8. All goods, edible grade 7. All goods other than edible grade 3. Crude glycerin 1. All goods 2. 0% - - 7. All goods 6. 0% - - 7. Raw Sugar Nil - 3. A 7. 7. 1. 70. 1 Refined or white sugar Nil - 3. B 7. 8. 1. 70. 1 Raw sugar if imported by a bulk consumer Nil - 3. C 7. 9. 1. 70. 2 Dextrose Monohydrate 2. Lactose for use in the manufacture of homeopathic medicine 1. All goods 2. 5% - - 8. All goods 1. 0% - - 8. All goods 3. 0% - - 8. Food preparations, for infant use and put up for retail sale, of– (i) goods of headings 0. Preparations for infant use, put up for retail sale 3. All goods 3. 0% - - 8. All goods 3. 0% - - 8. All goods 3. 0% - - 8. Cranberry products 1. Orange juice 3. 0% - - 9. Soya protein concentrate 1. All goods (excluding compound alcoholic preparations of a kind used for. By volume, determined at a temperature of 2. Any Chapter The goods specified in List 1 used in the processing of sea- food. Nil Nil 6 9. 4. 2. Wine, for use as sacramental wine 3. Nil 7 9. 5. 2. 20. All goods - Nil - 9. All goods 7. 5% - - 9. Angostura bitters 5% - - 9. Veterinary drugs and other goods specified in List 2 1. All goods 5% - - 1. Bran, sharps and other residues, whether or not in the form of pellets. Fin fish feed Nil - - 1. All goods 1. 5% - - 1. Dietary soya fibre 1. De- oiled rice bran oil cake Nil - - 1. All goods 2. 0% - - 1. Feed additives or pre- mixes 2. Prawn feed, shrimp larvae feed and fish feed in pellet form Explanation.- For the removal of doubt, "prawn feed"shall mean goods- . SION) for prawn feed as. Public Notice No. RE- 8. 8)/1. 99. 7- 2. June, 1. 99. 8 (as amended from time to time) of the Government of India, in. Ministry of Commerce and Industry. All goods 5% - - 1. Crude or unrefined sulphur 2. Rock phosphate 2. Gypsum 2. 5% - - 1. All goods Nil - - 1. Boron ores 2. 5% - - 1. Acid grade fluorspar 5% - - 1. The following goods, when imported for use in the manufacture of refractory. Chapters 3. 8, 6. A) (1) Aluminous cement (2) Silicon metal (9. Micro/fumed silica (4) Brown fused alumina (5) Sintered/tabular alumina (6) Fused zirconia (7) Sodium hexameta phosphate (8) Silicon carbide (9) Boron carbide (1. Reactive alumina (1. Fused silica; and (B) Phenolic resin 5% 5% - - 5 5 1. Gold ores and concentrates for use in the manufacture of gold Nil 2% 5 and 8 1. All goods 2. 5% - - 1. Nickel ore and concentrate Nil - - 1. Uranium concentrate (U3. Nil - - 1. 20. 2. All goods 5% - - 1. All goods 5% - - 1. Coking coal Explanation.- For the purposes of this exemption, "Coking coal" means. Swelling Index or Crucible. Swelling Number of 1 and above Nil - - 1. Steam Coal Nil 1% - 1. All goods other than those specified at S. Nos. 1. 22 and 1. Metallurgical coke Nil - - 1. Carbon black feed stock 2. All goods Nil - - 1. Avgas Nil - - 1. 29. Naphtha for the manufacture of polymers specified at S. Nos. 2. 37 to 2. 40. M/s Haldia Petrochemicals Limited(HPL) Nil - 5 1. All goods(including naphtha),other than goods mentioned at Sr. Nos. 1. 31. 1. 32, 1. Motor spirit commonly known as petrol 2. High speed diesel (HSD) 2. Naphtha, when imported by Ratnagiri Gas and Power Private Limited (RGPPL). Ratnagiri Gas. and Power Private Limited (RGPPL) at Dabhol, District Ratnagiri, Maharashtra. Nil Nil - 1. 34. 2. Naphtha, when imported for generation of electrical energy by a generating. Electricity Act, 2. Provided that the exemption shall not be available if. Electricity Act, 2. Nil - - 1. 35. 2. All goods Nil - - 1. All goods, for the manufacture of fertilisers Nil Nil 5 1. How to configure hybrid Azure Active Directory joined devices. With device management in Azure Active Directory (Azure AD), you can ensure that your users are accessing your resources from devices that meet your standards for security and compliance. For more details, see Introduction to device management in Azure Active Directory. If you have an on- premises Active Directory environment and you want to join your domain- joined devices to Azure AD, you can accomplish this by configuring hybrid Azure AD joined devices. The topic provides you with the related steps. Before you begin. Before you start configuring hybrid Azure AD joined devices in your environment, you should familiarize yourself with the supported scenarios and the constraints. To improve the readability of the descriptions, this topic uses the following term: Windows current devices - This term refers to domain- joined devices running Windows 1. Windows Server 2. Windows down- level devices - This term refers to all supported domain- joined Windows devices that are neither running Windows 1. Windows Server 2. Windows current devices. For devices running the Windows desktop operating system, we recommend using Windows 1. Anniversary Update (version 1. The registration of Windows current devices is supported in non- federated environments such as password hash sync configurations. Windows down- level devices. The following Windows down- level devices are supported: Windows 8. Windows 7. Windows Server 2. R2. Windows Server 2. Windows Server 2. R2. The registration of Windows down- level devices is supported in non- federated environments through Seamless Single Sign On Azure Active Directory Seamless Single Sign- On. The registration of Windows down- level devices is not supported for devices using roaming profiles. If you are relying on roaming of profiles or settings, use Windows 1. Prerequisites. Before you start enabling hybrid Azure AD joined devices in your organization, you need to make sure that you are running an up- to- date version of Azure AD connect. Azure AD Connect: Keeps the association between the computer account in your on- premises Active Directory (AD) and the device object in Azure AD. Enables other device related features like Windows Hello for Business. Configuration steps. You can configure hybrid Azure AD joined devices for various types of Windows device platforms. This topic includes the required steps for all typical configuration scenarios. Use the following table to get an overview of the steps that are required for your scenario: Step 1: Configure service connection point. The service connection point (SCP) object is used by your devices during the registration to discover Azure AD tenant information. In your on- premises Active Directory (AD), the SCP object for the hybrid Azure AD joined devices must exist in the configuration naming context partition of the computer's forest. There is only one configuration naming context per forest. In a multi- forest Active Directory configuration, the service connection point must exist in all forests containing domain- joined computers. You can use the Get- ADRoot. DSE cmdlet to retrieve the configuration naming context of your forest. For a forest with the Active Directory domain name fabrikam. CN=Configuration,DC=fabrikam,DC=com. In your forest, the SCP object for the auto- registration of domain- joined devices is located at: CN=6. CN=Device Registration Configuration,CN=Services,[Your Configuration Naming Context]Depending on how you have deployed Azure AD Connect, the SCP object may have already been configured. You can verify the existence of the object and retrieve the discovery values using the following Windows Power. Shell script: $scp = New- Object System. Directory. Services. Directory. Entry. Path = "LDAP: //CN=6. CN=Device Registration Configuration,CN=Services,CN=Configuration,DC=fabrikam,DC=com". The $scp. Keywords output shows the Azure AD tenant information, for example: azure. ADName: microsoft. ADId: 7. 2f. 98. 8bf- 8. If the service connection point does not exist, you can create it by running the Initialize- ADSync. Domain. Joined. Computer. Sync cmdlet on your Azure AD Connect server. Enterprise admin credential is required to run this cmdlet. The cmdlet: Creates the service connection point in the Active Directory forest Azure AD Connect is connected to. Requires you to specify the Ad. Connector. Account parameter. This is the account that is configured as Active Directory connector account in Azure AD connect. The following script shows an example for using the cmdlet. In this script, $aad. Admin. Cred = Get- Credential requires you to type a user name. You need to provide the user name in the user principal name (UPN) format (user@example. Import- Module - Name "C: \Program Files\Microsoft Azure Active Directory Connect\Ad. Prep\Ad. Sync. Prep. Admin. Cred = Get- Credential. Initialize- ADSync. Domain. Joined. Computer. Sync –Ad. Connector. Account [connector account name] - Azure. ADCredentials $aad. Admin. Cred. The Initialize- ADSync. Domain. Joined. Computer. Sync cmdlet: Uses the Active Directory Power. Shell module, which relies on Active Directory Web Services running on a domain controller. Active Directory Web Services is supported on domain controllers running Windows Server 2. R2 and later. Is only supported by the MSOnline Power. Shell module version 1. To download this module, use this link. For domain controllers running Windows Server 2. In a multi- forest configuration, you should use the following script to create the service connection point in each forest where computers exist: $verified. Domain = "contoso. Replace this with any of your verified domain names in Azure AD. ID = "7. 2f. 98. 8bf- 8. Replace this with you tenant ID. NC = "CN=Configuration,DC=corp,DC=contoso,DC=com" # Replace this with your AD configuration naming context. New- Object System. Directory. Services. Directory. Entry. Path = "LDAP: //CN=Services," + $config. NC. $de. DRC = $de. Children. Add("CN=Device Registration Configuration", "container"). DRC. Commit. Changes(). SCP = $de. DRC. Children. Add("CN=6. 2a. 0ff. Connection. Point"). SCP. Properties["keywords"]. Add("azure. ADName: " + $verified. Domain). $de. SCP. Properties["keywords"]. Add("azure. ADId: " + $tenant. ID). $de. SCP. Commit. Changes(). Step 2: Setup issuance of claims. In a federated Azure AD configuration, devices rely on Active Directory Federation Services (AD FS) or a 3rd party on- premises federation service to authenticate to Azure AD. Devices authenticate to get an access token to register against the Azure Active Directory Device Registration Service (Azure DRS). Windows current devices authenticate using Integrated Windows Authentication to an active WS- Trust endpoint (either 1. Note. When using AD FS, either adfs/services/trust/1. If you are using the Web Authentication Proxy, also ensure that this endpoint is published through the proxy. You can see what end- points are enabled through the AD FS management console under Service > Endpoints. If you don’t have AD FS as your on- premises federation service, follow the instructions of your vendor to make sure they support WS- Trust 1. Metadata Exchange file (MEX). The following claims must exist in the token received by Azure DRS for device registration to complete. Azure DRS will create a device object in Azure AD with some of this information which is then used by Azure AD Connect to associate the newly created device object with the computer account on- premises. If you have more than one verified domain name, you need to provide the following claim for computers: http: //schemas. If you are already issuing an Immutable. ID claim (e. g., alternate login ID) you need to provide one corresponding claim for computers: http: //schemas. Live. ID/Federation/2. Immutable. IDIn the following sections, you find information about: The values each claim should have. How a definition would look like in AD FSThe definition helps you to verify whether the values are present or if you need to create them. Note. If you don’t use AD FS for your on- premises federation server, follow your vendor's instructions to create the appropriate configuration to issue these claims. Issue account type claimhttp: //schemas. 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