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This technical writing training program will offer attendees an understanding of how the reporting process supports products in research, development, and in the marketplace. This virtual session will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train attendees on effectively reviewing and revising documents and assessing your audience, in effect producing effective written correspondence. Why Should You Attend: This course will address how to write effective correspondence and reports in support of your company's activities. Attendees will learn how to organize and deliver information for the intended audience. They will also learn how to write clear and readable documents, and h…

This training will review the best practices establishing and conducting a cleaning validation for reusable medical devices. It will also address the requirements of ANSI/AAMI ST 98. Why Should You Attend: Reusable medical devices continue to receive scrutiny from regulatory agencies both in the United States and internationally. Since the advent of ANSI/AAMI ST 98 there has been more clarity in how to perform these validations but it is still important to know the regulatory expectations to reduce the likelihood that submissions will not be accepted and require additional testing or worst case that the testing needs to be repeated. This presentation will address the most current expectations for cleaning validations of reusable medical devices that are performed in support of th…
Propel Kinase Biology Understanding to Increase Selectivity, Overcome Resistance and Find the Optimal Combination Partner to Develop Best and First-in-Class Kinase Targeted Drugs The kinase drug discovery field is at a pivotal moment, with recent breakthroughs from industry leaders such as Biogen, A-Alpha Bio, and Proxygen paving the way for exciting new approaches in targeting kinases, particularly in targeted protein degradation. However, with ongoing challenges including selectivity and resistance in small molecule inhibitors, these hurdles limit the therapeutic applications and call for in-depth discussions focused on innovative future strategies for kinase targeted drugs. Join us at the 3rd Kinase Targeted Drug Discovery Summit; the premier, target-specific conference designed to prov…
3rd Kinase Targeted Drug Discovery Summit

This webinar will teach attendees best practices for conducting effective quality audits to ensure regulatory compliance. Learn how to avoid potential pitfalls during the audit process. Why Should You Attend: Auditing is a critical function within a pharmaceutical or medical device company. Properly performed audits help to ensure that audited parties are operating in accordance with regulatory requirements, procedures, supply/quality agreements, etc. Ultimately audits are a key contributor in ensuring product quality and regulatory compliance. This webinar will help attendees understand the fundamental audit steps and how to perform them properly. It will focus on audit planning, audit conduct, audit findings, and the audit report. The importance of interview techniques, cr…

It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement. This webinar will offer attendees a comprehensive understanding of the same while emphasizing the different types of sterilizing filtration available and their application to your particular system. For instance, the application of sterile filtration to use-point compressed air will be discussed in detail. Why Should You Attend: This course will offer a broad review of: Different filtration media with the construction characteristics and properties of each detailed A typical pharmaceutical sterile filtration system with its individual components Engineering schemat…
Accelerate collaboration and partnering across neurology and psychiatry pipelines and technologies, to reduce risk, validate technologies, and deliver better biodistribution of safe and efficacious molecules to the CNS URLs:Tickets: https://go.evvnt.com/2758081-0?pid=185Brochure: https://go.evvnt.com/2758081-2?pid=185 Time: 8:00 AM - 5:00 PM Speakers: Antony Mattesich, Chief Executive Officer, Amphista, Dan Elbaum Chief Scientific Officer QurAlis, David Donabedian Executive Partner Longwood Fund, Eliseo Salinas Head of Research and Development Delix, Jenny Laird Vice President, Search and Evaluation Neuroscience Eli Lilly, John Mayfield Senior Vice President, Business Development and Strategy Flagship Pioneering, Jonathan Levenson Chief Scientific Officer FireCyte Therapeutics, Laxminaraya…
Neuroscience Innovation Pharma Partnering Summit
Over the past 12 months, liquid biopsy testing has continued to revolutionize diagnostics and personalized medicine; from the integration of AI and automation to elevate liquid biopsy capabilities, to the approval of MRD as an endpoint in Multiple Myeloma. Cementing its position as the world's leading forum for liquid biopsy specialists, the 9th Liquid Biopsy for Precision Oncology Summit returns to San Diego in February - with a refreshed agenda providing crucial insights spanning biomarker discovery to commercialization, and each critical step in between. Whether you're new to the field or a seasoned expert, join over 250 of the industry's top decision-makers from AstraZeneca, Amgen, Eli Lilly, AbbVie, BLOODPAC, Boundless Bio, and more to ensure you and your team are equipped with the in…
9th Liquid Biopsy for Precision Oncology Summit | February 18-20, 2025 | San Diego, California

AI can transform regulatory decision-making by enhancing efficiency, compliance, and accuracy in GMP-regulated industries, including pharmaceuticals, biotechnology, and medical devices. It addresses core challenges like regulatory submissions, risk assessments, audits, clinical trial optimization, and post-market surveillance while minimizing human error. Learning Objectives:- Decode the psychology behind human error. Navigate regulatory requirements for error management. Apply Root Cause Analysis and the Root Cause Determination Tool effectively. Establish and track human error metrics. Monitor CAPA effectiveness with AI-enhanced KPIs. Integrate AI for predictive error prevention. Key Areas of Application:- Streamlining Regulatory Submissions: Automation: AI-driven NLP tools generate…

This webinar will discuss the main regulatory regimes for medical devices in US, Canada, Brazil, Japan and Australia, how they differ from EU CE mark regulations and how to address compliance though a Medical Device Single Audit Program (MDSAP) and ISO 13486:2016 approach Description: The webinar will discuss in detail how to address the gaps between US, Canada, Brazil, Japan, Australia and EU ISO 13485:2016 requirements for: Management responsibilities Device marketing authorization Facility registration Measurement, analysis & improvement Adverse events & vigilance reporting Design and development Manufacturing and service controls Purchasing activities Why Should You Attend: Companies conducting business in various geographical regions have to address numerous s…

66, JW Marriott Hotel Marina, Al Marsa Street, Dubai, United Arab Emirates

As healthcare systems evolve, Pharmacoeconomics will remain a key discipline for guiding decisions that optimize outcomes, resource allocation, and the overall sustainability of healthcare.The MEPDPS 2025: Middle East Pharmacoeconomics and Drug Policy Summit 2025 will take place on 21-22 February at JW Marriott Hotel Marina, Dubai, UAE and has been meticulously crafted to serve as a dynamic platform for thought leaders, policymakers, and key stakeholders to exchange insights, share experiences, in the areas focused on healthcare policy, the HEOR in healthcare decision making, economic evaluations, VBHC, the implications of HTA, responses to Real-World Evidence, collaboration, affordability, and equity in healthcare, that enhance patient outcomes, ensure accessibility to innovative therapie…
Middle East Pharmacoeconomics and Drug Policy Summit 2025

Dusit Thani Dubai, Sheikh Zayed Road, Dubai, United Arab Emirates

The 9th Annual Dubai International Pediatric Neurology Congress is the leading congress in the region that gathers top speakers and experts to highlight the latest developments and innovations in the Pediatric Neurology practice. The congress will be a ground for interaction for healthcare professionals, including but not limited to; pediatric neurologists, neurologists, genetic and metabolic consultants, pediatricians, and other healthcare professionals. his congress will be emphasizing on all topics related to this vital specialty, from diagnosis to treatment of many pediatric neurological disorders such as Paediatric Epilepsy, Paediatric Neurocritical care, Autoimmune and Genetic disorders, Neuro-immunology disorders, Neuromuscular disorders, and much more. Join the 9th Annual Dubai Int…
9th Annual Dubai International Pediatric Neurology Congress

Standard Operating Procedures (SOPs) are a vital component of ensuring compliance with regulatory agency requirements for pharmaceutical manufacturing. Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood how the writing of a procedure can have a positive or negative impact on training. In this course you will learn the vital connection between the documentation and training spheres, and how to maximize this connection to improve the quality of both SOPs and training. Why Should You Attend: To learn the parameters of an effective SOP To distinguish a well-written SOP from a poorly written one To define processes better by effecti…
The marcus evans 19th Edition Project Portfolio and Resource Management Excellence for Pharma and Biotech conference taking place on 24-26 February, 2025, in Morristown, New Jersey, will bring together key industry leaders to explore the latest strategies to optimize the success of the portfolio and organization. Attendees will review novel and leading planning strategies and execution outcomes within project and portfolio management from their peers in an intimate and end user driven environment of networking, hands on demonstrations, and workshop / masterclass discussions. Attending This Premier marcus evans Conference Will Enable You to: Structure and simplify processes to maximize portfolio growth Balance financial & scientific value to ensure project portfolio alignment with stra…
19th Edition Project Portfolio and Resource Management Excellence for Pharma and Biotech conference
The marcus evans 12th Edition R&D Controlling and Performance Management conference taking place on 24-26 February, 2025, in Morristown, New Jersey, will bring together key industry leaders to explore the latest strategies to optimise investments, streamline decision-making, and accelerate transformation in R&D. This event is your gateway to understanding how to drive efficiency, foster cross-functional collaboration, and refine R&D processes to stay ahead in an increasingly competitive landscape. Don't miss out on this opportunity to empower your R&D team with the tools and knowledge to thrive in a rapidly evolving market. Attending This Premier marcus evans Conference Will Enable You to: Achieve Operational Excellence in a Global R&D Organization Measure Objectives t…
12th Edition R&D Controlling and Performance Management conference