Skip to main content
Category

News Archive

mccc-2323-logo

2017 Annual Dinner – Montgomery County Chamber of Commerce

By News Archive

mccc-2323-logo

June 13, 2017 – 6:00pm – 9:00pm

Bethesda North Marriott Hotel and County Conference Center 5701 Marinelli Road, North Bethesda, MD 20852

Tuesday, June 13 MCCC 58th Annual Dinner honoring Dr. Martine Rothblatt and United Therapeutics as the Visionary of the Year United Therapeutics Corporation is a bio-tech company focused on the development and commercialization of innovative products to address the unmet medical needs of patients with chronic and life-threatening conditions. They have five approved products on the market today and are in relentless pursuit of “medicines for life”®. Their overarching commitment to environmental sustainability is reflected in their new corporate office facility in Silver Spring. This seven-story, 108,000-sq.-ft., cutting-edge collaborative workspace aims to inspire people think out of today’s box and into the realm of tomorrow.

Read More
entrepreneurship-startup-desk-2-pixa

Startup Visa Alternative Gives Foreign Entrepreneurs A Workaround – All Tech Considered : NPR

By News Archive

entrepreneurship-startup-desk-2-pixa

Immigration advocates claim that about half of the most lucrative startups in America were founded by immigrants. But it’s complicated for a foreigner to start a company in America — there’s no such thing as a startup visa.

That’s why some entrepreneurs are “hacking the system” through a workaround that started as an experiment in Massachusetts and has expanded to five other states.

Read More
qiagen logo

QIAGEN Partners With Maccura to Localize and Commercialize GeneReader NGS System in China – MilTech

By News Archive

qiagen-logo

QIAGEN N.V. (NASDAQ: QGEN; Frankfurt Prime Standard: QIA) today announced the formation of a joint venture with Maccura Biotechnology Co., Ltd., a leading in vitro diagnostics (IVD) company in China. The joint venture, named MAQGEN plans to accelerate local adaptations, development and commercialization of the GeneReader NGS System in the rapidly growing clinical and clinical research markets in China. QIAGEN’s GeneReader NGS System is the world’s first complete Sample to Insight solution and makes the benefits of next-generation sequencing (NGS) accessible to any laboratory.

Read More
pieris-pharmaceuticals-inc-logo

PIERIS PHARMACEUTICALS AND ASTRAZENECA COLLABORATE TO DEVELOP AND COMMERCIALIZE ANTICALIN-BASED INHALED TREATMENTS FOR RESPIRATORY DISEASES

By News Archive

pieris-pharmaceuticals-inc-logo

Pieris today announced a strategic collaboration in respiratory diseases with AstraZeneca to develop novel inhaled drugs that leverage Pieris’ Anticalin® platform, including its lead preclinical drug candidate, PRS-060.

Anticalin molecules are engineered proteins which can mimic antibodies by binding to sites either on other proteins or on small molecules. They are smaller than monoclonal antibodies, offering the potential of direct delivery to the lung.

Read More
medical-doctor-medicare-image

What are the “three Cs” of connected health?

By News Archive

Medicine is a field slow to adopt an innovation; after all, you are dealing with people’s lives and there is a very high bar for discarding old ways. That said, a huge percentage of the medical community will agree that tradition has often hampered the adoption of new technologies that can significantly improve communication, collaboration, and community.

Read More
medimmune-logo

AstraZeneca’s Imfinzi (durvalumab) Receives US FDA Accelerated Approval for Previously Treated Patients With Advanced Bladder Cancer

By News Archive

medimmune-logo

AstraZeneca (LSE: AZN) and its global biologics research and development arm, MedImmune, today announced that the US Food and Drug Administration (FDA) has granted accelerated approval to Imfinzi (durvalumab). Imfinzi is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma (mUC) who have disease progression during or following platinum-containing chemotherapy, or whose disease has progressed within 12 months of receiving platinum-containing chemotherapy before (neoadjuvant) or after (adjuvant) surgery. Imfinzi is approved under the FDA’s accelerated approval pathway, based on tumour response rate and durability of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.

Read More

Search

You have successfully subscribed to the newsletter

There was an error while trying to send your request. Please try again.

BioHealth Innovation will use the information you provide on this form to be in touch with you and to provide updates and marketing.