Forbes: Drug Truths
MAY 15, 2023
In the midst of the Covid-19 pandemic, when thousands of people were dying on a daily basis, the hopes of the world rested on the biopharmaceutical industry for rapidly finding vaccines, antibodies and therapeutants.
Drug Discovery World
JUNE 7, 2023
Compared with traditional mRNA vaccine delivery platforms, the RALA platform has the added advantage of ease of scalability and logistics, including stability at room temperature. pHion’s pipeline also includes differentiated therapeutic vaccines for the treatment of ovarian (PTX_V5) and prostate (PTX_V3) cancers.
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The Pharma Data
NOVEMBER 24, 2020
24, 2020 – At least thee new COVID-19 vaccine candidates are already in the pipeline, will a roll-out expected early in the new year. “These are immune responses, so if you feel something after vaccination, you should expect to feel that. Vaccines work to fight disease by producing an immune response within the body.
Agency IQ
MARCH 25, 2024
The testimony of witnesses and the Senators themselves largely agreed on the designation, but diverged on questions of liability exemptions. high cholesterol, changes in liver enzymes, decreased immune response to vaccination, thyroid disorders, and cancer). The hearing also featured questions from BEN CARDIN (D-Md.),
The Pharma Data
DECEMBER 11, 2020
Marshals to Protect COVID-19 Vaccines. COVID-19 vaccines will be protected by U.S. Food and Drug Administration is expected to quickly give emergency authorization to Pfizer’s COVID-19 vaccine, which would be followed by an undertaking to distribute 3 million doses of the vaccine nationwide, CBS News reported.
PPD
JULY 6, 2023
From oncology clinical research to vaccine development , successfully executing and overseeing the many moving parts of a clinical trial may become overwhelming for sponsors to handle alone. CROs should also be able to supply a list of client references or customer testimonials to demonstrate its ability to accelerate development.
Agency IQ
JUNE 17, 2024
Finally, many doctors offered testimony that, as a result of the 2021 Non-Enforcement Decision, more women will suffer serious adverse events,” the court wrote. Had they not, FDA’s authority to regulate would likely have been strained considerably.
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