Ranbaxy Laboratories

Rothschild & Co hires Alex Mironov and Matthew O’Donnell as Managing Directors in North America

Retrieved on: 
Monday, August 7, 2023

Rothschild & Co announced today that Alex Mironov and Matthew O’Donnell have joined the Healthcare team as Managing Directors.

Key Points: 
  • Rothschild & Co announced today that Alex Mironov and Matthew O’Donnell have joined the Healthcare team as Managing Directors.
  • The senior hires represent the continued growth of the healthcare franchise and expansion of the firm’s presence and capabilities in the Northeast region within the Global Advisory business in North America.
  • They will report to Dominic Hollamby, Partner and Global Head of Healthcare, and Lee LeBrun, Partner and Head of Global Advisory, North America.
  • Mr. Mironov brings over 20 years of global experience in the healthcare and pharmaceutical sectors, spanning business development, M&A and corporate strategy, to Rothschild & Co.

Blame capitalism? Why hundreds of decades-old yet vital drugs are nearly impossible to find

Retrieved on: 
Thursday, July 20, 2023

Past public ire over high drug prices has recently taken a back seat to a more insidious problem – no drugs at any price.

Key Points: 
  • Past public ire over high drug prices has recently taken a back seat to a more insidious problem – no drugs at any price.
  • Patients and their providers increasingly face limited or nonexistent supplies of drugs, many of which treat essential conditions such as cancer, heart disease and bacterial infections.
  • The American Society of Health System Pharmacists now lists over 300 active shortages, primarily of decades-old generic drugs no longer protected by patents.

A generic problem

    • The problem boils down to the nature of the pharmaceutical industry and how differently the markets for brand and generic drugs operate.
    • Perhaps the clearest indication of this is the fact that prices of brand drugs in the U.S. are among the highest in the developed world, while generic drug prices are among the lowest.
    • But once the patent expires, the drug becomes generic and any company is allowed to manufacture it.

Outsourced production creates more supply risks

    • One of the consequences of generics’ meager margins is that drug companies outsource production to lower-cost countries.
    • While overseas manufacturers often enjoy significant cost advantages over U.S. facilities, such as easy access to raw materials and lower labor costs, outsourcing production at such a scale raises a slew of issues that can hurt the supply.
    • The COVID-19 pandemic underscored the country’s reliance on foreign suppliers – and the risks this poses to U.S. consumers.
    • To ensure domestic supplies, the Indian government restricted the export of medications, disrupting the global supply chain.

Low profits hurt quality

    • Manufacturing drugs to consistently high quality standards requires constant testing and evaluation.
    • A company that sells a new, expensive, branded drug has a strong profit motive to keep quality and production high.
    • That’s often not the case for generic drug manufacturers, and this can result in shortages.
    • Thus, any hiccup in production or shutdown due to quality issues can affect the entire market.

Repatriating the drug supply

    • It is hard to quantify the impact of drug shortages on population health.
    • However, a recent survey of U.S. hospitals, pharmacists and other health care providers found that drug shortages led to increased medication errors, delayed administration of lifesaving therapies, inferior outcomes and patient deaths.
    • Whether this approach is feasible on a broader scale is uncertain, but, in my view, it’s a good first attempt to repatriate America’s drug supply.

Antitrust Violation vs. Injury-in-Fact: A distinction that makes a difference

Retrieved on: 
Saturday, February 4, 2023

But private plaintiffs must make an additional showing: to establish antitrust ‘standing,’ private plaintiffs must prove that the antitrust violation caused harm to them.

Key Points: 
  • But private plaintiffs must make an additional showing: to establish antitrust ‘standing,’ private plaintiffs must prove that the antitrust violation caused harm to them.
  • This distinction is deeply rooted in our system of antitrust enforcement, which permits many types of enforcers but limits standing to those with a cognizable claim of injury.
  • But when courts and litigants miss this doctrinal distinction on the road to resolving a case, it can have significant implications for antitrust law and policy.
  • The brief takes no position on the merits of the case, but instead explains that the district court missed the important distinction between an antitrust violation and an injury-in-fact.

Greenberg Traurig's Global Intellectual Property & Technology Practice Adds Life Sciences Patent Litigator Jay R. Deshmukh

Retrieved on: 
Thursday, January 5, 2023

NEW YORK, Jan. 5, 2023 /PRNewswire-PRWeb/ -- Global Law Firm Greenberg Traurig, LLP expands its global Intellectual Property (IP) & Technology capabilities with the addition of Jayadeep "Jay" R. Deshmukh as a shareholder in the New York office. He joins from Kasowitz Benson Torres and previously served as senior vice president of Global IP at Ranbaxy Laboratories, an international pharmaceutical company.

Key Points: 
  • Global Law Firm Greenberg Traurig, LLP expands its global Intellectual Property (IP) & Technology capabilities with the addition of Jayadeep "Jay" R. Deshmukh as a shareholder in the New York office.
  • NEW YORK, Jan. 5, 2023 /PRNewswire-PRWeb/ -- Global Law Firm Greenberg Traurig, LLP expands its global Intellectual Property (IP) & Technology capabilities with the addition of Jayadeep "Jay" R. Deshmukh as a shareholder in the New York office.
  • He joins from Kasowitz Benson Torres and previously served as senior vice president of Global IP at Ranbaxy Laboratories, an international pharmaceutical company.
  • I know the possibilities to grow my practice and benefit my clients are limitless here," Deshmukh said.

Global Antimalarial Drugs Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, 2018-2028

Retrieved on: 
Thursday, December 22, 2022

Key Points: 
  • Additionally, rise in malaria death cases, especially in developing nations are also fueling the growth of antimalarial drugs market.
  • Based on route of administration, the global antimalarial drugs market is segmented into oral, powder inhalation and intravenous administration.
  • • To analyze and forecast the market size of global antimalarial drugs market.
  • In this report, global antimalarial drugs market has been segmented into following categories, in addition to the industry trends which have also been detailed below:
    • Global Antimalarial Drugs Market, By Drug Type:

Arriello appoints distinguished regulatory expert, Pete Embley, as Chief Regulatory Officer

Retrieved on: 
Tuesday, November 29, 2022

DUBLIN, Nov.  29, 2022 /PRNewswire-PRWeb/ -- Arriello, a leading provider of integrated Regulatory Affairs, Pharmacovigilance and Auditing & QA solutions and services, has appointed respected regulatory expert Pete Embley as Chief Regulatory Officer, signalling the company's commitment to growing its pre-approval service line.

Key Points: 
  • DUBLIN, Nov. 29, 2022 /PRNewswire-PRWeb/ -- Arriello , a leading provider of integrated Regulatory Affairs, Pharmacovigilance and Auditing & QA solutions and services, has appointed respected regulatory expert Pete Embley as Chief Regulatory Officer, signalling the company's commitment to growing its pre-approval service line.
  • Pete, who joined Arriello in September and is based in Oxford in the UK, is the company's first Chief Regulatory Officer.
  • Accelerated pathways trigger an earlier and more intensive engagement with Regulatory agencies.
  • Pete has known Arriello since the company's inception, having previously worked with the co-founders Alan White and Anna Lukyanova.

Rx-360's Patient Safety Podcast: An Interview With Best-Selling Author Katherine Eban

Retrieved on: 
Tuesday, July 19, 2022

PHILADELPHIA, July 19, 2022 /PRNewswire/ --Rx-360 released the fifth episode of The Patient Safety Podcast, featuring an interview with Katherine Eban, contributing editor for Vanity Fair and a New York Times best-selling author.

Key Points: 
  • PHILADELPHIA, July 19, 2022 /PRNewswire/ --Rx-360 released the fifth episode of The Patient Safety Podcast, featuring an interview with Katherine Eban, contributing editor for Vanity Fair and a New York Times best-selling author.
  • "It took me a long time, but I uncovered the story of Ranbaxy, which was basically just an ongoing crime scene.
  • they eventually began a full-on chase scene where the inspector discovered the garbage bag was full of records of hidden defects," says Eban.
  • The bottom line for Eban is that good practice is "all about company culture and the leadership," and both need to act ethically to ensure patient safety.

SPAG, Leading Asian Integrated Health Communications and Marketing Agency, Joins FINN Partners

Retrieved on: 
Monday, July 18, 2022

NEW DELHI and NEW YORK and SINGAPORE, July 18, 2022 /PRNewswire/ --  Global independent marketing and communications agency FINN Partners announced today that SPAG, a leading, Asia-headquartered, health-sector communications and marketing firm with offices in Bangalore, Delhi, Indonesia, Malaysia, Mumbai, the Philippines and Singapore joins FINN Partners. SPAG serves global biopharma companies, health trade associations and health provider systems and is one of the region's top award-winning agencies. Aman Gupta, SPAG founder and managing partner, joins FINN as a managing partner and lead for the Agency's Health Practice throughout Asia.

Key Points: 
  • SPAG Founder Aman Gupta to Lead FINN Health Practice Throughout Asia; SPAG Co-Founder Shivani Gupta Appointed FINN Managing Partner, Culture and Brand Reputation, Health Asia
    NEW DELHI and NEW YORK and SINGAPORE, July 18, 2022 /PRNewswire/ -- Global independent marketing and communications agency FINN Partners announced today that SPAG , a leading, Asia-headquartered, health-sector communications and marketing firm with offices in Bangalore, Delhi, Indonesia, Malaysia, Mumbai, the Philippines and Singapore joins FINN Partners.
  • SPAG serves global biopharma companies, health trade associations and health provider systems and is one of the region's top award-winning agencies.
  • Aman Gupta, SPAG founder and managing partner, joins FINN as a managing partner and lead for the Agency's Health Practice throughout Asia.
  • SPAG Co-Founder Shivani Gupta, joins FINN as managing partner, Culture and Brand Reputation, Health Asia, and will focus on building brand communications and Practice culture throughout Asia.

CorMedix Inc. Announces the Appointment of Chief Executive Officer

Retrieved on: 
Thursday, March 17, 2022

Myron Kaplan, Chairman of CorMedixs Board of Directors commented, We are delighted to welcome Joe to CorMedix as the new Chief Executive Officer.

Key Points: 
  • Myron Kaplan, Chairman of CorMedixs Board of Directors commented, We are delighted to welcome Joe to CorMedix as the new Chief Executive Officer.
  • CorMedix has a strong late-stage pre-commercial asset in DefenCath with a compelling value proposition for patients in the hemodialysis community, said Mr. Todisco.
  • I join my colleagues in welcoming Joe to CorMedix as Chief Executive Officer.
  • I look forward to working closely with Joe as we seek to transform CorMedix to a commercial stage entity.

Hagens Berman: Sun and Ranbaxy Facing January Trial as Federal Judge Denies Summary Judgment in Generic Drug Overpricing Lawsuit

Retrieved on: 
Tuesday, November 23, 2021

The federal racketeering statute (RICO) and the Sherman Act, which underpin the claims in the lawsuit, require automatic trebling of damages as a punitive measure against violators.

Key Points: 
  • The federal racketeering statute (RICO) and the Sherman Act, which underpin the claims in the lawsuit, require automatic trebling of damages as a punitive measure against violators.
  • In his 40-page order issued Nov. 22, 2021, United States District Judge Nathaniel M. Gorton rejected two of Suns key defenses.
  • But the court reject[ed] defendants assertions that the fact that Ranbaxy never sold Valcyte and Nexium... is dispositive of the Sherman Act claims.
  • Attorneys say Ranbaxy recklessly stuffed generic drug approval queues with grossly inadequate applications, deceiving the FDA into granting tentative approvals to lock in statutory exclusivities to which Ranbaxy was not entitled.