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- FDA Loosens Rules for Overseas Drug Trials
- Merrill Goozner, a former Chicago Tribune reporter turned public-health advocate (he heads up the Integrity in Science Project at the Center for Science in the Public Interest), notes an interesting and almost wholly overlooked Food and Drug Administration decision that may have the effect of subjecting clinical-trial volunteers in poor...
- Blog posts 2008-05-08
- Astra Takes on Glaxo in U.S. COPD Drug Market
- By Ben Hirschler LONDON (Reuters UK) - AstraZeneca is seeking U.S. approval to sell its asthma drug Symbicort for chronic obstructive pulmonary disease (COPD), ramping up competition with GlaxoSmithKline's Advair. Both are inhaled drugs combining a corticosteroid and a long-acting beta-agonist. AstraZeneca said on Wednesday...
- News items 2008-04-30
- Cholesterol-drug Rejection Rips New Gash in Merck
- By Ransdell Pierson NEW YORK (Reuters) - Confidence in Merck & Co's (MRK) earnings prospects withered on Tuesday, along with its stock price, after U.S. regulators surprisingly rejected the drugmaker's treatment to raise levels of "good" HDL cholesterol. Shares of Merck,...
- News items 2008-04-29
- FDA to New Drugs: It's Hammer Time
- Wonder no further whether the recent litany of drug-safety problems would make the Food and Drug Administration more cautious about approving new drugs. In just the past four days, the agency has thrown some serious sand into the industry's drug-development works, delaying or derailing three separate programs of widely varying...
- Blog posts 2008-04-29
- Glaxo Wins U.S. FDA Approval For Wider Advair Use
- By Susan Heavey WASHINGTON (Reuters UK) - U.S. health regulators have said GlaxoSmithKline Plc's (GSK)(GSK) Advair is safe and effective to more widely treat patients with chronic obstructive pulmonary disease (COPD), the drugmaker said on Wednesday. Glaxo's approval comes the same day as rival AstraZeneca...
- News items 2008-04-30
- News May Need Waiver to Acquire Newsday
- Rupert Murdoch's plan to add Long Island's Newsday newspaper to his News Corp empire likely will become the next lightning rod in a debate over how US regulators decide on the number of media properties one company can own.If News Corp tries to buy Newsday, the company may ultimately...
- News items 2008-04-24
- Chinese Eye $15b Electricity Sell-off
- China's largest power company is eyeing the NSW government's $15 billion sell-off of the electricity industry.China Huaneng Group has already bought power assets in Queensland and Singapore, Fairfax reports, and now wants to greatly expand its presence in South-east Asia and Australia.The company has asked its "Australian team to...
- News items 2008-05-09
- Zuckerman Submits $580 Million Newsday Bid: Source
- By Robert MacMillan and Kenneth Li NEW YORK (Reuters) - New York Daily News owner Mortimer Zuckerman has submitted a $580 million bid for Tribune Co's Newsday daily newspaper on Long Island, New York, matching a bid by News Corp (NWSa) Chief Executive...
- News items 2008-04-26
- Why Biogenerics Will Survive Genzyme's Problems
- The Food and Drug Administration rejected Genzyme's request to sell a version of its drug Myozyme made in a new factory, a decision some journalists and bloggers insist on casting as a black mark against the very notion of generic biotech drugs. There's just one problem: These...
- Blog posts 2008-04-22
- Small-Business Freebies From The Government
- The federal government doesn't just collect taxes and look over our shoulders at our business practices. It has a number of organizations that actually help business. The old joke goes this way: We're from the government, and we're here to help you. But the truth is, the federal government really...
- White papers
- Meeting US FDA 21 CFR Part 11 Requirements
- The U.S. Food and Drug Administration (FDA) introduced 21 CFR Part 11 (Part 11) regulations to promote wide usage of electronic technology in the life sciences industry in a way that is compatible with FDA's responsibility to protect public health. MetricStream, the leading provider of compliance and...
- White papers
- SCORE Helps Technical Consultant Open Doors To New Markets
- Shirley Young was among the thousands of entrepreneurs who successfully rode the wave of the global technology boom. Her company, Global Advanced Technology, Inc. (GATI), provided engineering and management services to some of the nation's leading telecommunications and networking and fault-tolerant computing companies, and served as the U.S. distributor for...
- Case studies
- Expiring Terrorism Insurance Act Threatens to Leave Businesses Exposed
- The federal government's agreement to back companies that offer terrorism insurance expires at the end of the year, bringing the prospect of sky-high premiums and scarce coverage for local companies in 2006. The Terrorism Risk Insurance Act, or TRIA, was enacted three years ago in the wake of Sept. 11...
- White papers
- Standard Form 26, Award/Contract
- This is the form used by the federal government to award a contract, usually as a result of a Request for Quotation. Both parties sign, but it requires references to the basic solicitation and/or other documents. In general, this form is similar to Form 33, although it requires additional certification...
- Tools & templates
- Case Study: Enterprise Architecture in Action
- The Food and Drug Administration (FDA) faced several challenges after the President of U.S.A laid down the Management Agenda (PMA) as a framework for a citizen-centered, results-oriented, and market-based Federal government accomplished through five executive branch-wide initiatives. This study focuses on how the FDA Information Technology (IT) consolidation solution, driven...
- Case studies
- FDA Approves VELCADE (Bortezomib) for Injection for the Treatment of Relapsed and Refractory Multiple Myeloma
- This article discusses the Millennium Pharmaceuticals, Inc. approval from the U.S. Food and Drug Administration (FDA) to market VELCADE for the treatment of multiple myeloma patients who have received at least two prior therapies and have demonstrated disease progression on the last therapy. The effectiveness of VELCADE is based on...
- White papers
- Therapeutic Dose: At What Cost Quality?
- The U.S. has long laid claim to the safest, highest quality drug supply in the world. Indeed, under the aegis of the 65-year-old Food, Drug and Cosmetic Act, the pharmaceutical industry and the U.S. Food and Drug Administration have labored long and hard to build an extensive closed system of...
- White papers
- Armed Forces Recreational Center Uses federal government ESPC to Achieve Goals
- Shades of Green is a 216,050 square foot resort facility with 287 rooms. The resort is operated by the United States Army for the benefit of active and retired military personnel. Shades of Green is located at the Walt Disney World Resort. The project objective is to reduce operating costs,...
- Case studies
- Thermal Storage Retrofit Reduces Costs for Federal Building
- This 27-story structure is located in downtown Pittsburgh and was constructed in 1963. A wide range of federal government agencies occupies the building. The original 30-year old chiller plant consisted of two 990-ton centrifugal chillers equipped with open drives and reduction gears. By modern standards, the chillers were of comparatively...
- Case studies
- Sarbanes-Oxley Reality Check on Bureaucracy
- The Sarbanes Oxley Act was a politically motivated maneuver to take advantage of the disdain for Corporate Executives accused of fraud in the mass media court of public opinion. Yet all the real courts of law have acquitted most of the corporate executives of any wrongdoing. Except for Martha Stewart...
- White papers
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