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EVENTS

The Digital Pharma Advances
THE DIGITAL PHARMA ADVANCES
January 29-29, 2020
Powerfully Target & Engage HCPs & Patients & Deliver Real-World Results With Integrated, Innovative Digital Strategies.Customer-Centric, Value-Adding, Multi-Channel Digital Pharma Marketing Strategies.

4th Annual Microbiome Movement, Drug Development, Europe
4TH ANNUAL MICROBIOME MOVEMENT, DRUG DEVELOPMENT, EUROPE
February 04-05, 2020
As the first microbiome-based therapeutic steps closer to market approval, the scientific community continue to demonstrate the functional role of the human microbiome as a novel source of therapeutic, biomarker and diagnostic development. Despite this progress, the vast potential to develop effecti...

Terminus

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Terminus is the leader of the account-based movement and the crucial link that connects B2B marketing and sales teams with their ideal customers. The Terminus solution arms marketing teams with an account-centric platform that delivers the intelligence and automation needed to scale ABM and revolutionize the way B2B marketing is done. Hundreds of organizations worldwide, including Salesforce, GE, Verizon, 3M and CA Technologies, turn to Terminus to more effectively target, engage and grow their best-fit accounts. Terminus offers savvy marketers the technology and proven expertise to radically improve ABM strategies and campaigns, increasing ROI and producing exceptional results.
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RELATED NEWS


The National Institute for Health and Care Excellence has issued a final green light securing routine NHS funding for Roche’s Perjeta in patients with a certain type of breast cancer. The guidelines follow a confidential commercial agreement for Perjeta (pertuzumab) agreed between NHS England and the drugmaker late last year, paving the way for its move from the Cancer Drugs Fund (CDF) to the NHS’ routine commissioning stream, when used to treat advanced HER2-positive breast cancer. ...

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How bad is the generics market in the U.S. these days? Reports from some players are that it continues to be tough, but the picture will get a lot clearer when generics leader Teva reports Thursday, followed by Mylan next week. Indications are the short sellers are tuned in. Novartis provided an inkling of how competitive the U.S. generics remains when it reported last month that sales at its Sandoz generics unit were down 4%. Bernstein analyst Ronny Gal told investors in a note today that he ha...

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GlaxoSmithKline (GSK) has committed $120m to expand its biopharmaceutical manufacturing facility in Upper Merion, Pennsylvania, US. The investment is intended to fit the manufacturing facility with technologies that will offer the flexibility and speed required to produce complex speciality medicines to cater to the current market. GSK says the expansion will support essential assets in its pipeline, including therapies for cancer and other speciality diseases. All assets are undergoing clinical...

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EnvoyHealth, the independently operated subsidiary of leading specialty pharmacy, Diplomat, has added partnerships with two web-based services in the past month. Combined, the services promise to improve speed to therapy and adherence to drug regimens, in the near term, and a higher degree of patient satisfaction with therapy, especially in chronic conditions, in the longer term. Envoy itself is a patient hub, providing manufacturers a way to offer benefit verification, prior authorization and o...

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If you eavesdropped in Lions Health’s Palais II headquarters Tuesday morning, you heard a lot of chatter about who picked up awards the night before, and even more speculation on why. Outside in its sprawling cabana, Facebook was handing out sodas, water and trail mix along with client case studies. But onstage and in session, it was about patient-first marketing, data-gathering, technology tools and why we’ll all be friends with robots by 2028.Meanwhile, speakers were talking up cha...
FIERCEPHARMA
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The US Food and Drug Administration (FDA) has approved Jacobus’ Ruzurgi (amifampridine) tablets for the treatment of Lambert-Eaton myasthenic syndrome (LEMS) in patients six to less than 17 years of age. The approval marks the first FDA approval of a treatment specifically for paediatric patients with LEMS, as currently the only other treatment approved for LEMS is approved for use in adults. The approval was based on a placebo-controlled withdrawal study of 32 adult patients in which pati...

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EVENTS

The Digital Pharma Advances
THE DIGITAL PHARMA ADVANCES
January 29-29, 2020
Powerfully Target & Engage HCPs & Patients & Deliver Real-World Results With Integrated, Innovative Digital Strategies.Customer-Centric, Value-Adding, Multi-Channel Digital Pharma Marketing Strategies.

4th Annual Microbiome Movement, Drug Development, Europe
4TH ANNUAL MICROBIOME MOVEMENT, DRUG DEVELOPMENT, EUROPE
February 04-05, 2020
As the first microbiome-based therapeutic steps closer to market approval, the scientific community continue to demonstrate the functional role of the human microbiome as a novel source of therapeutic, biomarker and diagnostic development. Despite this progress, the vast potential to develop effecti...