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Pfizer’s Richard Connell On “Pausing” Anti-Infectives Research In China, And Taking A Long View On Asian Partnerships

 
• By Tamra Sami and Vikas Dandekar

On the way back to his old job in the U.S., after a stint in Shanghai as head of research Asia, Richard Connell says Pfizer is “pausing” plans for an anti-infectives research unit in China after hitting a few speed bumps.

HYDERABAD, India – En route back home to Groton, Connecticut from Shanghai, Pfizer Inc. Head of Preclinical Outsourcing VP Richard Connell met with PharmAsia News last month along the sidelines of the BIO Asia conference in Hyderabad, India, to talk about Pfizer’s research efforts in Asia. Connell had stepped in to take over as Pfizer’s head of research, Asia, following the departure of Steve Yang, a leading light in the China pharma world, who jumped to AstraZeneca PLC to rejoin his old boss Martin Mackay, Pfizer’s former R&D chief and current head of R&D at AZ (Also see "Pfizer Shake Up Continues With Key Exits From Emerging Markets" - Scrip, 10 December, 2010.)

In this interview, Connell shares his experiences in Shanghai and India, where Pfizer has partnered with local companies on preclinical...

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Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval

 
• By Neena Brizmohun

Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.

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• By Nielsen Hobbs

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• By Nielsen Hobbs

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Brazil Pilots Digital Drug Pack Inserts

 
• By Francesca Bruce

A new pilot aims to take Brazil closer to ‘digital transformation.’

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US FDA Could Seek Stronger Warnings On SSRI Antidepressant Risks During Pregnancy

 
• By Sue Sutter

Testimony during a July 21 ‘expert panel’ could help justify stronger warnings across the class about potential adverse effects on mother and baby. Panelists ranged from clinicians who said depression during pregnancy should be treated, to those who said sadness has been “medicalized."

World’s First Hemato-Oncology Microbiota Therapeutic Among Latest New EU Filings

 
• By Neena Brizmohun

The European Medicines Agency has started reviewing for potential EU marketing approval six new products, including MaaT Pharma’s microbiota therapeutic for acute-graft-versus-host disease, and AstraZeneca's camizestrant for locally advanced or metastatic breast cancer.

Sponsors Asked, EMA Delivered: One Handbook To Navigate CTIS

 
• By Vibha Sharma

The European Medicines Agency has revised the sponsor handbook for the Clinical Trials Information System, bringing together guidance that was previously scattered across multiple platforms and documents to help sponsors navigate the trial process more efficiently.