Camargo

NOVEMBER 29, 2021

The development of biological products (or biologics) represents a major advancement in modern medicine, enabling the treatment of patients with many illnesses where no other therapeutics were previously available. Small molecules have known structures and are primarily chemically synthesized. ADME and Dosing Regimen.

Development 180

Development Protein Production Hormones 180

pharmaphorum

AUGUST 24, 2020

Lynne was previously employed at Roche Biomedical Laboratories, the University of Maryland at Baltimore’s School of Medicine, and earned her B.S. Key sessions include: • Evaluating the ongoing Complications of Personnel Derived Contaminations. SMi’s 3rd Annual Pharmaceutical Microbiology Conference will no longer take place in Boston.

Contamination 52

Contamination In-Vitro Production Containment 52

XTalks

NOVEMBER 7, 2022

Liquid biopsy tests in oncology involve isolating entities such as circulating tumor cells (CTC), circulating tumor DNA (ctDNA) and tumor-derived exosomes. These tumor-derived entities are used to derive genomic and proteomic data. The same webinar held a Q&A session with Dr. Bahassi and two other experts from Medpace, Dr. Lyon L.

Clinical Trials 98

Clinical Trials Clinical Trials Trials FDA Approval 98

Cloudbyz

AUGUST 19, 2024

Food and Drug Administration (FDA), the European Medicines Agency (EMA), and various other national and international organizations oversee the approval, monitoring, and post-market surveillance of medical devices. However, the benefits of these devices come with significant responsibilities to ensure they are safe, effective, and reliable.

Compliance 52

Compliance Manufacturing Regulation Marketing 52

The Pharma Data

MAY 4, 2021

Internal Medicine. Raises Full-Year 2021 Guidance (3) for Revenues to a Range of $70.5 Billion and Adjusted Diluted EPS (2) to a Range of $3.55 Now Anticipates Revenues of Approximately $26 Billion for BNT162b2, Reflecting 1.6 Billion Doses Expected to be Delivered in 2021 Under Signed Contracts as of Mid-April 2021. per share amounts).

Vaccination 40

Vaccination Vaccine Production Sales 40

XTalks

OCTOBER 8, 2024

The approval was awarded to Abbott’s Alinity m MPXV assay, the first mpox in vitro diagnostic (IVD) listed under the WHO’s Emergency Use Listing (EUL) procedure. It is intended for use by trained clinical laboratory professionals skilled in PCR techniques and IVD procedures. Mpox has led to at least 635 deaths in the DRC this year.

In-Vitro 98

In-Vitro DNA Contamination Manufacturing 98

XTalks

JANUARY 6, 2025

Whether its the integration of nanotechnology in medicine, the evolution of point-of-care (POC) diagnostics or the transformative impact of CRISPR and regenerative medicine, these biotech trends are pushing scientific boundaries and creating new opportunities for businesses and researchers alike.

Gene Therapy 111

Gene Therapy RNA Gene Editing Gene 111