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BioWorld - Wednesday, June 10, 2026
Home » Authors » Mari Serebrov

Mari Serebrov

Articles

ARTICLES

Impact of Shutdown Depends on How Long It Lasts

Oct. 2, 2013
By Mari Serebrov
With both the House and Senate refusing to be the first to flinch in their ongoing game of chicken Tuesday, the rest of America was getting a feel for how the first government shutdown in 17 years might affect their day-to-day businesses.
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It’s How You Look at the Vial

Oct. 1, 2013
By Mari Serebrov
What’s in a biosimilar name? That depends on whether the vial is half empty or half full. Seeing it as half full, many generic makers focus on the similarities between a follow-on and its reference biologic. Because of those similarities, they say biosimilars and their reference product should share the same international nonproprietary name (INN) – as is the practice with traditional generic drugs. That’s the argument the Generic Pharmaceutical Association (GPhA) made in the citizen petition it submitted to the FDA earlier this month. Used to cashing in on the success of a small molecule brand drug by sharing...
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U.S. Government is Too Big to Shut Down Completely

Oct. 1, 2013
By Mari Serebrov
As the U.S. House and Senate continued their down-to-the-wire game of chicken Monday, government departments dusted off and updated their contingency plans in preparation for what threatened to be the first shutdown in nearly two decades should neither side give on a continuing resolution to fund federal programs after 12:01 a.m. (EDT) Tuesday, the dawn of fiscal 2014.
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The Federal Drug Tracking System Is Moving Toward Reality

Sep. 27, 2013
By Mari Serebrov
A national track-and-trace system that would preempt the expanding patchwork of state regulations involving the drug supply chain may soon move a step closer to reality.
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FDA: 505(q) Petitions Simply Way to Delay Competition

Sep. 26, 2013
By Mari Serebrov
Prioritizing 505(q) petitions asking the FDA to take or stay action in pending approvals of biosimilars, generics and 505(b)(2) drugs is delaying action on more important matters, the agency told Congress in a recently submitted annual report.
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Senators: CMS Policy Crucial to Antibiotic Development

Sep. 25, 2013
By Mari Serebrov
When it comes to health care, money really does talk – especially if it’s in the form of Medicare reimbursement.
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Angels Eye the Devil in SEC’s Rule 506 Changes

Sep. 24, 2013
By Mari Serebrov
Given the devil in the details of the SEC’s amendments implementing Title II of the Jumpstart Our Business Startups (JOBS) Act, some angels fear that what Congress intended as a way to help start-ups raise money before going public could make participating in Rule 506 private offerings even riskier.
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GPhA: Common Name is Key to Biosimilar Competition

Sep. 23, 2013
By Mari Serebrov
What’s in a name? Marketability. That’s part of the sales pitch the Generic Pharmaceutical Association (GPhA) made in a citizen petition in which it asked the FDA to give biosimilars the same international nonproprietary name (INN) as their reference biologic.
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Drugmakers Look to Supreme Court for Clarification, Shields

Sep. 20, 2013
By Mari Serebrov
With the Supreme Court beginning its next session later this month, drugmakers are looking to the justices for guidance in shareholder, whistleblower and patent infringement cases while seeking protection from punitive damages and some civil suits.
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JOBS Act Succeeds in Jumpstarting Bio IPOs

Sep. 19, 2013
By Mari Serebrov
In the wake of the Jumpstart Our Business Startups (JOBS) Act, more than 230 initial public offerings (IPO) are expected this year, with small biotechs and other emerging growth companies (EGCs) accounting for much of the resurgence in IPO interest.
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View All Articles by Mari Serebrov

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