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World Health Organization Resolves to Improve Clinical Trials Globally

  • Post author:PacConAdmin
  • Post published:May 31, 2022
  • Post category:Drug Industry Daily

In an effort to prepare for future health emergencies, the World Health Organization (WHO) has adopted a resolution geared toward delivering higher quality data and improving the conduct and coordination…

Continue ReadingWorld Health Organization Resolves to Improve Clinical Trials Globally

J&J Sues Aurobindo Pharma Over Proposed Generic Prostate Cancer Drug

  • Post author:PacConAdmin
  • Post published:May 31, 2022
  • Post category:Drug Industry Daily

Johnson & Johnson (J&J) has filed a complaint against Aurobindo Pharma charging the Indian generics maker with infringing on patents for J&J’s blockbuster prostate cancer therapy Erleada (apalutamide). Source: Drug…

Continue ReadingJ&J Sues Aurobindo Pharma Over Proposed Generic Prostate Cancer Drug

GSK Buys Affinivax in $3.3B Deal, Nets Two Vaccine Candidates and Novel Technology

  • Post author:PacConAdmin
  • Post published:May 31, 2022
  • Post category:Drug Industry Daily

GSK announced yesterday that it is acquiring Cambridge, Mass.-based biopharma company Affinivax in a $3.3 billion deal, picking up at least two novel pneumococcal vaccine candidates and a promising vaccine…

Continue ReadingGSK Buys Affinivax in $3.3B Deal, Nets Two Vaccine Candidates and Novel Technology

Senate User Fee Package Addresses Accelerated Approval, Rare Disease Issues

  • Post author:PacConAdmin
  • Post published:May 27, 2022
  • Post category:Drug Industry Daily

The Senate’s bill to reauthorize FDA user fee programs for drugs, biologics and medical devices, introduced last week by Sen. Patty Murray (D-Wash.) and Sen. Richard Burr (N.C.), includes proposed…

Continue ReadingSenate User Fee Package Addresses Accelerated Approval, Rare Disease Issues

Senators Push FDA and PTO to Coordinate Better on Drug Patents That Could Delay Generics

  • Post author:PacConAdmin
  • Post published:May 27, 2022
  • Post category:Drug Industry Daily

A bipartisan pair of senators — Maggie Hassan (D-N.H.) and Bill Cassidy (R-La.) — are pressing federal agencies to close oversight gaps that delay generic drugs and in turn keep…

Continue ReadingSenators Push FDA and PTO to Coordinate Better on Drug Patents That Could Delay Generics

Topline Data Support NDA for Zealand’s Treatment for Rare Childhood Hypoglycemia Disorder

  • Post author:PacConAdmin
  • Post published:May 27, 2022
  • Post category:Drug Industry Daily

Zealand Pharma will bring a new form of its antihypoglycemia drug Zealogue (dasiglucagon) to the FDA as a potential treatment for children with congenital hyperinsulinism (CHI). Source: Drug Industry Daily

Continue ReadingTopline Data Support NDA for Zealand’s Treatment for Rare Childhood Hypoglycemia Disorder

HHS Kills the Trump Rule Requiring Agencies to Reassess Regulations Every 10 Years

  • Post author:PacConAdmin
  • Post published:May 27, 2022
  • Post category:Drug Industry Daily

The Department of Health and Human Services (HHS) has withdrawn a controversial and unpopular Trump-era final rule that would have required federal health agencies to reassess their regulations every 10…

Continue ReadingHHS Kills the Trump Rule Requiring Agencies to Reassess Regulations Every 10 Years

Teva and Allergan Reach $161.5 Million Opioid Settlement With West Virginia

  • Post author:PacConAdmin
  • Post published:May 26, 2022
  • Post category:Drug Industry Daily

Teva Pharmaceuticals and Allergan will pay more than $161 million to the state of West Virginia to settle allegations that the companies contributed to the opioid epidemic. Source: Drug Industry…

Continue ReadingTeva and Allergan Reach $161.5 Million Opioid Settlement With West Virginia

Cantwell, Grassley Introduce Senate Bill to Control PBMs’ Pricing Practices

  • Post author:PacConAdmin
  • Post published:May 26, 2022
  • Post category:Drug Industry Daily

Sens. Maria Cantwell (D-Wash.) and Chuck Grassley (R-Iowa) introduced a bill this week that directs the Federal Trade Commission (FTC) to hold pharmacy benefit managers (PBM) accountable for allegedly deceptive…

Continue ReadingCantwell, Grassley Introduce Senate Bill to Control PBMs’ Pricing Practices

Form 483 Docks Clinical Formula for Inadequate Quality and Laboratory Controls

  • Post author:PacConAdmin
  • Post published:May 26, 2022
  • Post category:Drug Industry Daily

The FDA issued skincare drug product developer Clinical Formula a five-observation Form 483 for lacking an effective quality control unit and other serious deficiencies observed during a November-December 2021 inspection…

Continue ReadingForm 483 Docks Clinical Formula for Inadequate Quality and Laboratory Controls
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