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Coronavirus: Health workers' army to be trained to deliver Covid vaccine

The Pharma Data

The Department of Health and Social Care (DHSC) said this could include training a wider range of existing NHS staff, as well as student doctors and nurses. A rapidly-developed vaccine for H1N1 swine flu in 2009, Pandemrix, was linked to a small number of people developing chronic sleep disorder narcolepsy. Source link.

Vaccine 52
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Genomics/Biobanks/Cohort Studies

Broad Institute

Known to be a regulator of metabolism, we have found that in addition it has profound behavioral effects in animals and humans, even evident in population-level economic behavior. in Physics from Massachusetts Institute of Technology in 2009. With this proposal, we will add a measure of thyroid hormone, T3, to the assessment battery.

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Meet the Patient Advocate Panelists in Our Upcoming Webinar: Rare Disease Day 2023 Wrapped, What You Need to Take Away

Conversations in Drug Development Trends

I joined the FARA staff in 2009, and our team built a nationwide series of bike rides called rideATAXIA to raise funds for research. At Canary Advisors , we concentrate on patient-focused drug development, making sure sponsors, regulators, and other key stakeholders can better align with what’s most meaningful to patients.

Disease 52
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How Lume Whole Body Deodorant Was Inspired by a Genetic Disease

PLOS: DNA Science

Among the barrage of drug ads for cancer, diabetes, weight loss and more are those for Lume , a “doctor-developed whole body deodorant.” The earliest patent I found was issued in late 2009, for “Products and Methods for Reducing Malodor from the Pudendum.” ” For everyone. .” ” Lady parts.

Disease 76
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Women in STEM: An Inspiring Journey with Dr Jo Brewer

Drug Target Review

It set a precedent with regulators as to what is expected in some instances. Success in the haematology space has really been driving this from the beginning, which is not surprising as haem doctors understand stem cell transplants; they’re used to working with a lot of the sort of toxicities that can come with cell therapies.

Therapies 115
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Time for FDA’s OPDP to Fill the Gaps on Digital and Social Media

Eye on FDA

Then as part of the agency’s effort at putting together a regulatory stance regarding the unique questions posed by the huge migration into digital and social communications, FDA later that year posed a series of five questions to inform the regulation of this burgeoning environment during a public meeting held that same year.

FDA 52
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Raising Welfare for Lab Rodents

Codon

This is due, in part, to perceptions of public safety, and by extension, regulation. So, whereas a gene-edited feeder mouse or agricultural animal might take years to clear FDA regulations, an animal that has been bred for higher welfare would not. Another reason to favor breeding has to do with attitudes toward gene editing.

Research 113