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farma-industrie

GARDP, Eisai & Takeda partner in search for new antibiotics

The Global Antibiotic Research and Development Partnership (GARDP), Eisai Co., Ltd. and Takeda Pharmaceutical Company Limited have signed an agreement for GARDP to access and screen components of Eisai and...

Pharma Biz

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wet- en regelgeving

FDA approves new drug to treat adults with relapsing forms of MS

The U.S. Food and Drug Administration today approved Mayzent (siponimod) tablets to treat adults with relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and...

News-Medical.Net

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marketing

Hoe ziet de marcom-branche er in het post-coronatijdperk uit?

Marcom-branche Hoe gaan we de marketingcommunicatie-branche straks na corona vormgeven? Er zijn verschillende scenario’s denkbaar, waarvan er één mijn voorkeur heeft en één absoluut niet. Lees meer over: Hoe ziet de...

Marketingfacts.nl

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wet- en regelgeving

AstraZeneca’s infant respiratory drug prioritised in Europe, U.S.

Britain’s AstraZeneca said a potential medicine to prevent respiratory syncytial virus (RSV) in babies and infants had been granted special status by U.S. and European regulators, designed to speed up the...

Reuters Health

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wet- en regelgeving

FDA approves AbbVie’s Mavyret for children with Hepatitis C (HCV)

The FDA has approved AbbVie’s Mavyret tables (glecaprevir/pibrentasvir) as a treatment for hepatitis C (HCV) in children aged 12 to 17 years old. AbbVie’s two drug combo tablets have been approved as a treatment for all...

InPharm.com

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marketing

Contentmarketing is geen vakgebied, maar een mindset

We draaien rondjes. Wat is nou precies contentmarketing? Ik kan je verklappen: alles, zolang je de consument op de eerste plek zet.

Adformatie Nieuws

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onderzoek

GSK’s ovarian cancer treatment meets main goal in late-stage study

GlaxoSmithKline said on Monday a late-stage study testing its initial maintenance therapy, Zejula, in patients with ovarian cancer who have undergone platinum-based chemotherapy showed positive results.

Reuters Health

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wet- en regelgeving

Eton’s conjunctivitis treatment fails to win FDA nod; shares tumble

Eton Pharmaceuticals Inc said on Friday that the U.S. Food and Drug Administration declined to approve its treatment for conjunctivitis, sending its shares tumbling nearly 20 percent in extended trading.

Reuters Health

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onderzoek

Researchers identify opportunities to advance genomic medicine

Genomic medicine
New study highlights milestones in the history of genetic discoveries; equitable and fair access required to address disparities.

EurekAlert

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marketing

[column] Marketing zonder ziel is dodelijk

Misha Stoutenbeek is marketingadviseur en copywriter. Hij beschouwt in zijn blogs alledaagse marketingpraktijken. In deze aflevering wordt hij geconfronteerd met een merk zonder menselijke kant, marketing zonder passie.

MarketingTribune

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Latest articles

GARDP, Eisai & Takeda partner in search for new antibiotics

FDA approves new drug to treat adults with relapsing forms of MS

Hoe ziet de marcom-branche er in het post-coronatijdperk uit?

AstraZeneca’s infant respiratory drug prioritised in Europe, U.S.

FDA approves AbbVie’s Mavyret for children with Hepatitis C (HCV)

Contentmarketing is geen vakgebied, maar een mindset

GSK’s ovarian cancer treatment meets main goal in late-stage study

Eton’s conjunctivitis treatment fails to win FDA nod; shares tumble

Researchers identify opportunities to advance genomic medicine

[column] Marketing zonder ziel is dodelijk

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