Monday, July 27, 2026
Institutional expertise

Experts powering global pharma intelligence

A focused editorial team with pharma, regulatory, and market backgrounds delivering actionable industry intelligence worldwide.

AI-assisted analysis validated by human pharmaceutical experts.

Industry credibility

5 Editorial experts
60+ Years combined experience
40+ Regulatory agencies tracked
12,000+ Research reports published

Expertise coverage

Therapeutic, regulatory, and commercial depth across global markets

  • FDA & EMA regulation
  • Clinical trials
  • AI in pharma
  • Oncology pipelines
  • Manufacturing intelligence
  • Market access
  • Biosimilars
  • Pharmacovigilance

Editorial Team

Editors and analysts with pharma, regulatory, and market backgrounds

Michael Rodriguez

Managing Editor

Former Reuters Health

Expertise FDA Approvals · Biotech · Breaking News

14+ years in pharma

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Journalist specializing in FDA approvals and biotech coverage. Previously covered pharma and biotech for Reuters Health.

James Park

Regulatory Affairs Editor

Former Pfizer

Expertise FDA · EMA · Global Pathways

12+ years in pharma

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Writes on FDA, EMA, and global regulatory pathways, translating submissions, approvals, and guidance into actionable intelligence.

Robert Kim

Senior Science Editor

Former Genentech

Expertise Immunotherapy · Oncology · Science Writing

11+ years in pharma

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Science editor covering oncology, immunotherapy, and mechanism-of-action explainers for a professional pharma audience.

Sophie Martin

Market Analysis Editor

Former McKinsey

Expertise Market Access · Pricing · Competitive Intel

8+ years in pharma

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Covers pharmaceutical market dynamics, pricing, market access, and competitive intelligence.

Published intelligence

2,478+ Articles published Global intelligence
68+ Whitepapers analyzed Research library
220+ Events covered Conferences & summits
40+ Regulatory agencies FDA · EMA · PMDA · more

Editorial integrity

All content is reviewed by regulatory, scientific, and industry specialists before publication. AI-assisted analysis is validated by human pharmaceutical experts.

  • Multi-source verification for regulatory and clinical claims
  • Expert review for high-impact intelligence and breaking alerts
  • Transparent correction policy within 24 hours
  • Clear separation of editorial and sponsored content

Our methodology combines regulatory monitoring, conference intelligence, research library analysis, and editorial validation — positioning NovaPharmaNews closer to institutional intelligence than media blogging.

Global coverage network

🇺🇸 US · FDA 🇪🇺 EU · EMA 🌏 APAC · PMDA/NMPA 🌎 LATAM · ANVISA+

Connect with our team

General inquiries

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Press & media

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Editorial

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