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How to Interview Healthcare Experts to Write Exceptional Website Content

Healthcare Success

In today’s blog post, I share an effective editorial workflow you can implement today between your healthcare marketing agency and medical experts. Evidence-based: Medical information should be based on research and studies—not opinions or anecdotes. An editorial workflow can be beneficial for various reasons. This is crucial.

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EMA’s CHMP recommends Bristol Myers Squibb’s Breyanzi approval

Pharmaceutical Technology

The regulator’s positive opinion was based on the data obtained from the pivotal Phase III TRANSFORM trial. The final decision from the European Commission (EC) is expected within around two months of receipt of the CHMP opinion, and will be applicable to all EU member states, Liechtenstein, Norway and Iceland.

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EMA CHMP recommends Moderna’s Covid-19 booster for children

Pharmaceutical Technology

The EMA positive opinion is based on clinical findings of mRNA.1273.214, Editorial content is independently produced and follows the highest standards of journalistic integrity. Topic sponsors are not involved in the creation of editorial content. 1273.214, a bivalent Omicron-targeting Covid-19 vaccine of the company.

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Court Rules FDA Must Divulge Internal Deliberations on Vanda’s Hetlioz sNDA

Pharma Leaders

Don’t waste your time on unending, unproductive online searches for news stories, reports and opinion; let DID’s experienced in-house editorial team do the work for you. Use your energy where it’s needed most — ensuring that your products are in compliance and getting to market as quickly as possible.

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FDA Considers Biomarker Data Supportive of Tofersen Approval

Pharma Leaders

Don’t waste your time on unending, unproductive online searches for news stories, reports and opinion; let DID’s experienced in-house editorial team do the work for you. Use your energy where it’s needed most — ensuring that your products are in compliance and getting to market as quickly as possible.

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CDER Flags Enforcement Successes for Fiscal 2022

Pharma Leaders

Don’t waste your time on unending, unproductive online searches for news stories, reports and opinion; let DID’s experienced in-house editorial team do the work for you. Use your energy where it’s needed most — ensuring that your products are in compliance and getting to market as quickly as possible.

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Candel and the University of Pennsylvania to assess solid tumour therapies

Pharmaceutical Technology

In September, Candel received a positive opinion from the European Medicines Agency (EMA) Committee for Orphan Medical Products (COMP) on the application seeking orphan drug designation for CAN-2409 for treating glioma patients. Editorial content is independently produced and follows the highest standards of journalistic integrity.