Virtual Events Pharmacology

The industry is currently experiencing a resurgence in viral vector characterization, driven by biopharma investment and new regulatory frameworks. Advanced analytical technologies are crucial in dealing...

Join our live webinar to discover how Lokavant's Clinical Trial Intelligence Platform utilizes AI and machine learning to optimize study performance. Learn how real-time analytics can assess trial progress,...

Join us for a Midwest Chapter meeting and CE event with Dr Skoch. He will present on Buprenorphine, covering its history, pharmacology, pharmacokinetics, and considerations for pain and opioid use disorder....

Since the introduction of the new pharmacovigilance legislation in the EU, QMS and self-audits have become an increasingly important topic. Companies have been challenged by regulators to implement risk-based...

Healthcare professionals delivering geriatric care must be highly skilled clinicians. They need expertise in pharmacology updates, managing challenging geriatric behaviors, infectious diseases, dementia...

ICBB2023 aims to provide an innovative and comprehensive overview of BIOTECHNOLOGY and BIOENGINEERING, a focus will be given to major research advances including: 1. Microbiology, virology, cytology and...

The importance of drug and medical device safety is paramount and the regulations and requirements applicable to the discipline of pharmacovigilance are extensive and complex. This course has been designed...

Participate in our upcoming live webinar to gain comprehensive knowledge about our Master's programs at the second-ranked school of Pharmacy and Pharmacology globally.

Jo... discusses the challenges associated with using organoids in drug discovery, highlighting their increasing popularity due to their superior disease modeling capabilities compared to traditional...

In recent years, there has been a shift from traditional pen and paper methods to remote and digitized data capture in healthcare. Additionally, there has been a focus on incorporating the patient's perspective...

Earn Continuing Education Credits (CEs) and learn from renowned faculty members. Utilize best practices for clinical trials during outbreaks involving High Consequence Pathogens (HCPs) and prevent risks...

of patient-centricity and clinical trial enrollment, providing valuable insights and strategies for a more efficient and impactful recruitment process.

Pharmacovigilance regulations in Asia are dynamic and fast-changing. As the Asia-Pacific region becomes increasingly important for pharmaceutical companies, it's vital to ensure compliance and safety by...

The Latin America Regulatory compliance requirement training/webinar focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics, Biosimilars,...

There is a great desire to discover novel therapies for non-alcoholic steatohepatitis (NASH), now referred to as metabolic-associated steatohepatitis (MASH), due to the urgent need for effective treatment...

As somatic cell and gene therapy platforms advance, regulatory guidelines from the FDA and ICH also progress. Adhering to these guidelines is crucial to minimize delays in clinical trial development. Each...

This meeting focuses on using computational chemistry and synthetic methodology to explore chemical space and create new functional molecules for solving problems in organic chemistry, drug discovery,...

Attend this webinar to learn about recent advances in covalent drug discovery, including targeted covalent modulators that have been approved by the FDA or are in late-stage clinical trials. The speaker...

The Montgomery–Åsberg depression rating scale (MADRS) and the Hamilton depression rating scale (HDRS or HAM-D) are commonly used in mood disorder clinical trials. It is advised for raters to use the...

This summit will bring together senior leaders in the biopharma industry to share exclusive data on lipid nanoparticles, a non-viral delivery system with potential in various fields. Attendees will gain...

This intensive two-day course will look at the various topics and their practical application from the perspective of compliance with the requirements of the Regulatory Authorities. The course will include...

BioPharma Webinars provides high-quality webinars presented by respected individuals in the pharmaceutical, biopharmaceutical, biologics, and biotech industries to keep its global audience informed on...

During clinical development, new drug candidates undergo essential studies to determine optimal treatment doses, confirm efficacy, and complete the drug's filing dossier. These studies include drug labeling...

United Scientific Group (USG) invites scholars, scientists, dental practitioners, and other experts to the International Conference on Dental Science and Research in Paris. The event offers networking...

Learn how to achieve long-term success with decentralized clinical trials by starting small and focusing on early wins. Join this webinar to discover the positive results they are driving in the industry....

The conference program allows presenters enough time to cover their subject thoroughly and engage in meaningful discussions with the audience.

The transition from manual data entry to automatic data acquisition in clinical trials is now essential. Sponsors who embrace eSource gain advantages such as faster access to data, shorter trial timelines,...

Our pharmaceutical trainings provide a thorough understanding of regulatory elements. PK/PD modeling predicts drug effects and is a valuable tool in drug candidate selection and clinical study design....

The regulatory requirements for Biological drug products are complex, and pharmaceutical companies are continuously under pressure to ensure regulatory compliance from drug discovery to post-marketing...