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In this ISSUE

Pharm Exec's Brands of the Year 2017

Scott Gottlieb's Multiple FDA Challenges

Leadership: Failure is an Option

Top Story
UK Political Parties Set Out Pharma Plans Ahead of Election
With the UK's General Election set for next week, Leela Barham looks what the competing parties are promising for pharma and healthcare
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2017 Real-World Evidence Benchmark Survey
Deloitte's 2017 Real-World Evidence Benchmark Survey shows that life sciences companies are making some progress in using RWE but still have opportunities to expand applications across the value chain, consider new channels to access RWD, and improve their overall capabilities.
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Europe
A Long Summer of Drug Pricing Tension Looms
In the hothouse atmosphere of European governments' anxieties over ever more expensive medicines, recent weeks have seen perspiration breaking out on the brows of ministers, officials and drug company executives, writes Reflector
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The Importance of Stakeholder Research in Rare Disease Drug Development
The approval of novel orphan drug designations continues to grow, while many existing rare disease therapies are receiving approval for expanded indications. With this increase Rare Disease Drug Development and broadening class of products, including some that target the same mutation or molecular defect, sponsors face new and significant market access challenges in securing reimbursement. Sponsored by Covance
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Call for Nominations
Pharm Exec's Emerging Pharma Leaders 2017 — Nominate Here
Read here for details of how to nominate a colleague — or yourself — for Pharm Exec's annual Emerging Pharma Leaders feature
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Launch Excellence V: Surviving and thriving in a specialized world
Live Webinar: Wednesday, June 14 at 10:00am EDT
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Regulatory
FDA Looks to Advance Regenerative Medicine
The Center for Biologics Evaluation and Research (CBER) is gearing up to facilitate the development and approval of regenerative medicine advanced therapies, as defined by the 21st Century Cures Act, writes Jill Wechsler
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Emerging Biopharma and Rare Disease: Finding a Needle in a Haystack
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Calendar
/ June 6–7: Pharmaceutical Compliance Congress Canada /
Toronto, CA
/ June 22–23: Patient Engagement Solutions Summit /
Philadelphia, PA
/ June 27–28: Publication and Clinical Trial Transparency /
Barcelona, Spain
/ August 8–9: Bio/Pharma Strategic Portfolio Management Summit /
Cambridge, MA
/ September 14–15: Risk Based Global Monitoring 2017 /
Barcelona, Spain
/ October 24–25: 12th Annual Value-Based Oncology Management /
Scottsdale, AZ
/ February 27–28, 2018: Speaker Programs 2018 /
Philadelphia, PA
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Through the Patient's Eyes - Needs, Behaviors and the Science Behind it All
Live Webcast: Wednesday, June 21 at 11:00am EDT
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Coming to terms with Patient Centricity
Live Webinar: Tuesday, June 20 at 12:00pm EDT
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Competitive Advantage
Reinventing the Role of Medical Affairs
As digital technologies transform drug development and marketing, a retooled medical affairs function can be a competitive differentiator, write Loic Plantevin, Christoph Schlegel and Maria Gordian
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Talking the Patients' Language – the importance of effective, patient-centered engagement
Live Webinar: Tuesday, June 6 at 8:00am EDT
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Outlook
Pharma & Biotech Forecast: Outlook Sunny, But Uncertain
Peter Young presents a summary of the strategic issues facing the biopharma industry, reviews recent M&A and financing activity, and looks at the implications for senior management
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Industry update
//Constellation Pharmaceuticals (Cambridge, MA) appointed Jigar Raythatha as President and CEO. //Concert Pharmaceuticals (Lexington, MA) announced that Ryan Daws, Chief Financial Officer, will be leaving the company in early June 2017 to return to investment banking. //Genecentric Therapeutics (Durham, NC) appointed Walter M. Capone as Chief Business Officer and added Ellen Lubman to its Board of Directors. //Rosa & Co. (San Carlos, CA) appointed Matt Marano as Senior Vice President of Business Development//
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Winning the RAT race: A new Center of Excellence to drive development of regenerative medicines
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