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May 24, 2018

Today's Rundown

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Featured Story

GlaxoSmithKline veteran Zhi Hong launches Brii Biosciences with $260M

Armed with a trio of partnerships and $260 million in the bank, Brii Biosciences' mission is to overcome the challenges that have prevented the spread of innovative medicines throughout China.

Top Stories

Bloom bags cash, UCLA tech to treat epilepsy via the microbiome

Bloom Science has raised seed money and licensed technology to treat CNS diseases via the gut-brain axis. Building on research into the ketogenic diet, Bloom is initially focusing on developing bacterial treatments for epilepsy.

Astellas to halt work at R&D subsidiary amid restructuring plan

Astellas Pharma has begun restructuring its operations, with plans to discontinue all work at its R&D subsidiary of about 200 employees by March 2019. An early retirement incentive program is estimated to cut 600 staff altogether, in the face of exclusivity losses expected to cause a dip in operating profits next year.

[Sponsored] Growing Requirements for Medicines for Children

Progress has been made in developing medicines for children with the passing of pediatric regulation, but gaps still exist. Here’s what you need to know about recent updates from an expert at Synteract.

Aptinyx seeks $80M IPO to push NMDA drug platform

With the ink barely dry on a partnership deal with Allergan, Aptinyx has announced plans for an $80 million IPO to accelerate work on its drugs for neurological disorders.

Novo Nordisk licenses kidney disease drug from Epigen

Novo Nordisk has picked up the worldwide rights to a kidney disease drug in development at Epigen. The agreement gives Novo control of orally available LPA1 receptor antagonist EPGN696 in exchange for up to $200 million in upfront and milestone payments.

Curis hires former Tesaro CMO Robert Martell as head of R&D

Curis is bringing on board member Robert Martell as a full-time employee in the newly created role of head of R&D. Martell was formerly chief medical officer at Tesaro, after serving as director of global oncology research at Bristol-Myers Squibb.

Resources

[Whitepaper] Compliance Certificate and Training for Life Sciences Professionals

4-day interactive educational program trusted by multi-national companies as part of their compliance training for employees. Explore legal, regulatory and ethical issues faced by pharmaceutical, biotech and medical device manufacturers operating globally. Visit event homepage for session topics.

[Whitepaper] Choosing the Best Steriles Dosage Form for Your Phase I Clinical Supply Needs

There are many parenteral dosage forms from which the pharmaceutical scientist can choose to develop their drug product. In this article, the author discusses the choices available and strategies which can be employed at the different stages of development.

[Whitepaper] Risk-based Approach to Change Management of GxP Systems

Learn how to reduce change management burden, keep systems current, and maintain compliance by applying a risk-based approach to change management of GxP systems.

[Whitepaper] Regulatory Transformation at UCB

UCB took a more holistic approach to managing regulatory processes. Read how their efforts are paying off.

[Whitepaper] Five Tracking Spreadsheets it’s Time for Regulatory to Retire

Find out how to eliminate regulatory’s tracking spreadsheets for good.

[Whitepaper] A Simpler Approach to RBM in Clinical Trial Management

Learn how cloud-enabled solutions provide real-time insights and actionable analytics to improve clinical trial safety and performance in this short presentation.

[Whitepaper] Digitizing the Global Life Sciences Supply Chain: The Critical Role of Digital Transaction Management

Life science companies are experiencing a significant transformation in how they bring new products to market.

Events

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