Normally License Crawler works wonders on almost every machine I try it on. This issue is about to make me pull my hair out. When I had a couple of problems activating office, I tried a reinstall from the account ( same account for many installs ), and found out that the key on the box is NOT the key registered on the account!! I tried using the using the script to get the last five digits, I could not find the installer for the install I did and ended up activating over phone.I haven't yet had to do a full reinstall, so say if a machine is replaced and I cant run the script, or possibly, if as William5230 did, I may have used the same key on several machines, my question would be, how can I reinstall from a boxed retail product key when there is no corrollation between the box key and the install key?I am currently creating a new account for each install and logging that into the future against our customer account. Yes, BoAlthough with my installs, we buy the retail version and use the key from the box. Extra 1.Then install the Office package at the computer, knowing you are home safe if you or your customer forgets either login or changes mail address or whatever.MS wants to sell 365 solutions, not OEM -).‘Karenge Poore,Sapne Adhoore’ the CSR initiative of Indo count. ![]() Rajit Kapur on how to say goodbye to eyeglasses.This Mother's Day, colour the walls with your kid.Cognizant kicks off $400 million cost-cut plan.Billionaire Mukesh Ambani’s Reliance has stock analysts most bullish in seven years.After wooing pilots, IndiGo & AI eye 55 Go First aircraft. ![]() Adani Enterprises to weigh stock sale months after Hindenburg turmoil.SC to Sebi: Can't give 6 months more for Adani probe.Failure to correct these violations may also result in the FDA refusing admission of articles manufactured at the Indrad plant into the US, it added. ![]() "Until you correct all violations completely and we confirm your compliance with CGMP, FDA may withhold approval of any new drug applications or supplements listing your firm as a drug manufacturer," the letter said. While acknowledging that the company has hired a consultant, the regulator asked it to engage a consultant that could assist the firm in meeting CGMP requirements. ![]() The regulator has asked the company to provide a retrospective, third-party review of all invalidated results for products currently in the US market and within expiry as of the date of the letter, and a report summarising the findings of the analysis. "Repeated failures at multiple sites demonstrate that executive management oversight and control over the manufacture of drugs is inadequate," it added. The USFDA also cited a similar CGMP observation for inadequate investigations at the company's Dahej facility at an inspection during March 11-19, 2019. Stating that company's investigations into testing results were inadequate, the letter said this is a repeat observation from USFDA's April 17-28, 2017, inspection at the Indrad facility. Another issue raised by the regulator was that the drug firm failed to thoroughly investigate any unexplained discrepancy or failure of a batch or any of its components to meet any of its specifications, whether or not the batch has already been distributed. In a warning letter issued by the regulator to Torrent Pharma's CEO Samir Mehta, the regulator said, "Your firm failed to follow written procedures for production and process control designed to assure that the drug products you manufacture have the identity, strength, quality, and purity they purport or are represented to possess." It asked the company to provide a detailed summary of its validation program for ensuring a state of control throughout the product lifecycle, along with associated procedures. The United States Food and Drug Administration (USFDA) had inspected the facility from April 8 to 16, 2019. New Delhi, Oct 17 () The US health regulator has red flagged Torrent Pharmaceuticals for significant violations of current good manufacturing practice (CGMP) regulations at its Indrad facility in Gujarat.
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