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Pharma Microbiology East Coast Conference – A Virtual Conference with Remote Access

pharmaphorum

SMi Reports: SMi Group have made the decision due to travel restrictions to open the conference and workshops to all microbiologists by transforming it into a virtual-remote online access event only on October 28 and 29 2020. Workshop B- Mycoplasma testing by anyone, anywhere and anytime! Workshops: October 30th, 2020.

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BioNTech, InstaDeep showcase early warning system for COVID variants

pharmaphorum

The algorithm looks at the structure of the SARS-CoV-2 spike protein used to gain entry to host cells, looking for changes that could enable the virus to evade immunity, as well as other features that could affect the ‘fitness’ of the virus – its ability to reproduce and transmit between people.

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TIGIT Therapies 2021

pharmaphorum

Plus 2 add on workshops: • Elucidating the anti-tumor immunity of other immune checkpoint inhibitors in oncology. Ensure your research team secures its place at the forefront of the immune checkpoint inhibitor space by putting this event on the calendar for 2021. . • Utilizing biomarkers to maximize the clinical effect.

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SMi’s 3D Cell Culture Conference 2021 – Speakers Announced

pharmaphorum

In addition to the agenda, there will be two pre-conference interactive workshops on: Workshop A – 08.30 – 12.30 on How to Develop Physiologically Relevant Immune Competent Models in MPS, led by Pelin Candarlioglu, Investigator – Bioengineer/Cell Biologist, GSK. Workshop B – 13.30 – 17.30 — ENDS –.

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3rd Cell Engager Summit

pharmaphorum

Modulate the immune system to drive efficacy via co-stimulatory targets to drive efficacy in solid tumors with Xencor, Harbour Biomed, Crescendo Biologics, Pieres, and Aptevo. Join our exclusive pre-conference workshop hosted by MacroGenics focused on ‘ Risk Mitigation in Translation & Clinical Development of Cell Engagers ’.

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What Do Patients Have to Say about Gene Therapy Trials? An Upcoming FDA Public Meeting to Hear from Patients and Caregivers

The FDA Law Blog

To further expand patient input into product development, the FDA’s Center for Biologics Evaluation and Research (CBER) Office of Therapeutic Products or “OTP” (formerly the Office of Tissues and Advanced Therapies, or “OTAT”) is holding a free public workshop titled, Clinical Trials: The Patient Experience.

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OPQ’s 2023 Annual Report: an Upbeat Review of CDER’s Quality Efforts

The FDA Law Blog

It also noted that last year, FDA hosted a two-day public workshop and published a white paper on the regulatory framework for Artificial Intelligence in drug manufacturing, in addition to other efforts. This strikes us as another signal that FDA sees the policies of cGMP as evergreen, and largely immune to even seismic technology shifts.

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