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The Mitochondria-Targeted DrugDevelopment Digital Summit (April 27-29) is the only industry-led meeting focused on end-to-end mitochondria-targeting. Join your peers this spring to collaborate and share learnings, whilst evaluating your clinical development landscape.
By Sarah Wicks — On May 21, 2024, the EveryLife Foundation for Rare Diseases (ELF) will host a Scientific Workshop at the National Press Club in Washington, D.C. aimed at identifying and characterizing the challenges in developing therapies for ultra-rare diseases and conditions that affect exceedingly small populations.
The Non-Small Cell Lung Cancer (NSCLC) DrugDevelopment Summit is the definitive industry-led forum for drugdevelopment in the largest solid tumor indication. The post Non-Small Cell Lung Cancer DrugDevelopment Summit appeared first on. View the event guide now for more details!
Program partners with government hospitals to strengthen drugdevelopment in the country Roche Pharma India has announced the launch of its clinical trial excellence project in India with an objective to strengthen the capabilities of public health institutions to do clinical trials and drug research in the country.
Workshops: 29 April 2022. SMi’s 5th Annual Pharmaceutical Microbiology East Coast Conference is taking place in Boston on April 27-28, 2022, with interactive workshops on April 26, 2022. Workshop Leader: Fred Ohsiek, SME, Cleaning Validation, North America. Workshop B: USP Microbiology 2022 – Keeping Up with Standards.
Bauer, Senior Regulatory Drug Expert & James E. Valentine — Incorporating patient and caregiver experiences into every phase of drugdevelopment has become increasingly prioritized during both development and review ( see, e.g. , previous coverage here ). By Larry J.
These are exactly the types of things that were addressed at ELF Scientific Workshop in May 2024 which addressed challenges in developing therapies for ultra rare diseases (see our blog about this here , which includes a link to the recording).
Paradigm Shift in DrugDevelopment: Analytical Quality by Design and Analytical Procedure Life Cycle In today’s pharmaceutical manufacturing environment, companies face increasing pressure to respond to changing demands across the global medicines supply chain while still maintaining the quality of their drug products.
hosted a series of workshops with patients, patient organizations, industry, and other stakeholders to develop a document known as the ‘Patient Experience Dossier’ (PED). In addition, patient experience data has also been included as part of the 21 st Century Cures Act which would assist the U.S.
Pepa has 15 years of combined experience in Regulatory Affairs (CMC) and multiple aspects of drugdevelopment and research and has participated in the approval of 15 original and biosimilar biologic license applications, focusing on microbiology product quality and sterility assurance aspects. Workshop: October 30th, 2020.
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 –.
The inaugural Next Generation Kinase Inhibitors Summit is the only industry-focused meeting dedicated to applying novel kinase biology to drugdevelopment and innovating existing programs to produce the next wave of kinase inhibitor drugs that are able to show efficacious and durable clinical response in oncology and beyond.
Arora explains that pharma associations like the Indian Pharmaceutical Association (IPA) organise training and development programmes through sessions, workshops, and webinars focused on the latest trends and technologies in R&D.
Enhance capital efficiency to re-invest in drugdevelopment programs. Panel Discussions, Workshops and Case studies on how the industry is tackling the Covid-19 crisis and implement social distancing in the lab. 2 On-Demand Workshops to optimize your facility design, and implement digitalization & LIMS.
The 5th Annual Targeted Protein Degradation Summit returns to Boston as the most comprehensive, definitive event of the year, uniting 700+ large pharma, innovative biotech and world-renowned academics to discuss the full breadth of protein degrader drugdevelopment.
The inaugural LNP Formulation & Process Development Summit is the industry’s first forum dedicated to bringing together drugdevelopers within the LNP field to share the latest scientific breakthroughs on formulation and process development. Join 80+ of your peers and be part of this growing community.
In 2021, LifeArc held a workshop (PDF) to explore the opportunities and challenges of repurposing drugs, developing a toolkit with the Medical Research Council (MRC). billion after selling a portion of its royalty interest in Merck & Co’s blockbuster cancer drug Keytruda to a pension fund.
By the end of Q2 FY 2023, FDA will convene the first of a series of 5 public meetings or workshops with key stakeholders including patients, biopharmaceutical companies, DHT companies, and academia to gather input into issues related to the use of DHTs in regulatory decision-making.
Gunnar Esiason, Senior Director, Head of Patient Engagement and Patient-Centered Innovation, at Raven (RA Ventures) will discuss the critical importance of early patient engagement in drugdevelopment from an investors perspective, highlighting the need for patient voices.
and other countries to help guard against potential drug shortages and medicines supply chain disruptions. Implementing such innovation will take time, however, in part because of obstacles that some drugdevelopers and manufacturers can face when considering whether to adopt PCM.
The scientific community will gather to discuss the translational challenges hindering drugdevelopers working on different drug delivery approaches, and explore new approaches, such as gene therapy, to identify potential clinical success. 3-day Conference | June 28-30, 2021.
Championing formulation excellence Similar to Roquette’s other Innovation Centers, the new US facility is dedicated to furthering the field of pharma science through cross-industry collaboration, research-led product development and a drive to improve patients’ lives.
For example, in March 2023, FDA issued a Framework for the Use of Digital Health Technologies in Drug and Biological Product Development , which noted that FDA would publish guidance on the use of DHTs in both traditional and decentralized clinical trials.
Table 2: Applications of Virtual Technology in Pharmacy Education AR VR MR XR Metaverse Virtual Laboratories √ √ 3D Anatomy and Physiology Visualization √ √ √ √ √ Drug Information and Interaction Visualizations √ √ √ Medication Administration Training √ √ √ Pharmacy Workflow and Practice Simulations √ Disease Simulation √ Medication Labeling and Packaging (..)
Though practices outlined in the guide are not official USP quality standards and are not intended to be binding or considered to be the only acceptable approach, they may be useful in developing PCM processes and facilitating adoption of PCM. Who should use the guide?
If you look at companies like Amazon and Google, the big tech companies, whenever they’ve gone into drugdevelopment on that side, they’ve found it incredibly hard. On the second day, he will be running a workshop on patient centricity. It’s very risky; it’s very hard to do.
From discussions on branded drugdevelopments to sessions hosted by major players like Pfizer and Novartis , there’s always something to learn. Look for local meetups, industry workshops, and smaller conferences that offer discounted early-bird rates. Actionable Insight: Post relevant questions or comments during these events.
This could include workshops, webinars, and online resources that provide insights into cultural competence in research settings. To support these enhancements, the NHC recommends the development of a comprehensive training module for IRB members and ethics committees that covers the nuances of evaluating informed consent materials.
This will give you access to industry expert-led courses, scientific workshops, and mentoring opportunities. In these courses, new employees learn about various types of regulatory documents, in-house templates, style guides, the drugdevelopment process, and more. Also, let’s not forget about virtual communication.
Regular workshops can ensure alignment and make your digital integration smoother. The potential to dramatically accelerate drugdevelopment, enhance research accessibility, and generate more nuanced, real-world data is compelling leaders to reimagine how medical investigations are conducted.
Rutta Chief Executive Officer 1 National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Health Sciences Policy; Forum on Drug Discovery, Development, and Translation. Innovation in drug research and development for prevalent chronic diseases: proceedings of a workshop.
Drugdevelopment. Exploratory development. Interactive Workshop on Friday 6 May 2022 on… Molecular and Cellular Pathophysiology of Pain Resolution. Workshop Leaders: Luda Diatchenko, Canada Research Chair in Human Pain Genetics, Department of Anesthesia, Faculty of Medicine, McGill University.
We brought our A-game with a workshop led by our Head of Content Strategy and Enablement, Prasant Vijayakumar. Through a diverse array of panels, keynotes, and interactive workshops, participants immersed themselves in the forefront of technological advancement. “Unveiling the Future: The Quest for Complete Content Automation.”
However, countries around the globe are at various stages of development for their regulatory policies. It can be overwhelming to know where to start to address nitrosamine impurities in drug products. Before the COVID pandemic, industry issues like this were often dealt with in a silo.
The workshop, coordinated by Dr Jitendra Kumar, MD, BIRAC and Alokparna Sengupta, MD, HSI/India, brought together academia, industry, government, and regulatory bodies to strategise the driving innovation factors in the sector and attract investments.
These advances can potentially bring new drugs to the population sooner and that applies to treatments for arthritis, cancer, and cardiovascular disease. A crucial step in the drugdevelopment process is testing on in-vitro cell cultures, which traditionally involve growing cells on a flat surface, such as a microscope slide.
Informa Connect's Access USA March 18-20, 2025, Pre-Event Workshops on March 17 Drug Channels readers save 10%* on their registration with code 25AUSA10 Three events. Rare Disease Summit Download Agenda While the industry has seen heightened focus surrounding rare drugdevelopment, weve only scratched the surface.
CBERs approach here was to take FAQs from across sponsor interactions, public workshops, email requests, etc. However, as your high-school literature teacher warned youto ace the test, you need to read the book, ahem, source regulations, guidance, or other policy documents.
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