Symmetric Training

Exciting News! 🎥 We’re thrilled to share an invitation from our trainer, James Drinkwater, for the upcoming online training course: Aseptic Fill & Finish of Biologics! 🚀 In this video, James highlights the key topics and insights you’ll gain from the course. Whether you’re looking to sharpen your skills or stay ahead of industry trends, this course is designed for you—don’t miss out! #AsepticProcessing #FillAndFinish #OnlineTraining #SymmetricTraining

Ongoing Training: Bioassay Development Today marks the final day of our bioassay development training! After mastering key guidance and best practices, participants have explored study design concepts, learnt about the principles of DoE, built robustness into assays, and analysed a bioassay validation case study. Today, we’ll delve into various statistical analysis methods, exploring when to apply each, with more case studies and an engaging group exercise. #drugdevelopment #analyticalmethods #bioassays #bioassaydevelopment #onlinetraining

Mastering Risk Management in Medical Device Development: Why It’s Vital 💡 In the fast-paced world of medical devices, ensuring patient safety and regulatory compliance is non-negotiable. Effective risk management is key to achieving these goals. Our latest blog explores the critical strategies and systems needed to manage risks throughout the development process. Whether you're working with ISO 14971 or seeking to enhance product safety, this is a must-read! 📊 If you're in medtech, quality assurance, or regulatory affairs, don’t miss out! Read the full article here 👇 #MedicalDevices #Pharma #ISO14971 #OnlineCourses #SymmetricTraining

Upcoming Online Training Courses – Starting Soon! 🎯 Elevate your expertise with our industry-leading online training courses designed for professionals in pharma & biotech! Here’s what’s coming up: 1️⃣ Paediatric Drug Development and Clinical Trials  This 2-day course covers medical, regulatory, ethical, organizational, and practical aspects of designing and conducting paediatric clinical trials. 2️⃣ Aseptic Processing in Manufacture of Sterile Products & ATMPs This 3-day online training covers GMP regulations and expectations for aseptic manufacturing of sterile medicinal products and ATMPs. 3️⃣ Lipid-Based Formulations The course covers lipid-based formulation principles, modified and targeted release mechanisms, and compares this drug delivery platform with others. Don’t miss out! Secure your spot today via the link in the comments. 📩 #ClinicalTrials #SterileManufacturing #OnlineCourses #SymmetricTraining

Ongoing Training: Process Scale-up, Validation & Tech Transfer for Biologics This week, our online training on ‘Process Scale-up, Validation, and Technology Transfer for Biologics’ is live! Participants are gaining insights into overcoming regulatory and technological challenges in biologics development. After a strong start with QbD principles and process development on day one, today's focus is on scale-up principles and an in-depth exploration of tech transfer. Stay tuned for more updates! #drugdevelopment #scaleup #technologytransfer #biologicsdevelopment #onlinetraining

Exclusive Sneak Peek of Our Upcoming CMC Statistics Presentation 👇 In this 3-day course, you'll see examples of statistical methods commonly used in CMC submissions to define sampling and acceptance criteria, inform process control, manage patient risk, and ensure ongoing product quality. In this presentation, you'll find insights on: 🔹 DOE for Design Space: Evaluate multiple responses and factor influences. 🔹 Equivalence Margins: Learn how to establish process compatibility. 🔹 Variance Component Analysis: Understand the impact of variability on processes. 🔹 Data Visualization: Discover how to analyze dissolution variability with visual tools. 🔹 Shelf Life Modeling: Learn advanced methods to estimate product shelf life. And so much more! To find out everything, visit the link in the comment section. #CMC #statistics #pharma #biotech #OnlineCourses #SymmetricTraining

Are you ready for the latest regulatory updates in medical devices❓ Stay ahead with our upcoming training courses focused on drug-device combination products and inhalation drug products. These courses are essential for professionals in the medical device and pharmaceutical industries looking to sharpen their regulatory expertise. Drug-Device Combination Products: Quality & Regulatory Requirements 📅 Date: 10 - 12 December 2024 📍 Venue: Live Online Training CMC and Regulatory Requirements for Inhalation Drug Products 📅 Date: 11 - 13 February 2024 📍 Venue: Live Online Training #CombinationProducts #Pharma #OnlineCourses #SymmetricTraining

Drug development is one of the most challenging paths in pharma. Despite years of research and promising preclinical results, only about 1 in 10 drug candidates make it through the rigorous clinical trial process to approval. ⚠️ Safety concerns often arise during Phase I or II trials, when drugs are first tested in humans, revealing side effects that weren’t evident in earlier stages. 💊 Lack of efficacy in real-world patients is another leading reason many drugs fail, especially in Phase II and III trials, where proving effectiveness is crucial. 🏛️ Regulatory hurdles are another challenge. Even if a drug is safe and effective, navigating the complex approval process requires extensive data and time. 💸 Finally, the high financial costs of clinical trials often force companies to halt drug development if the ROI isn’t clear. This high failure rate highlights the need for innovation! 💡 AI, precision medicine, and advanced trial designs are helping to improve success rates, streamline processes, and bring new treatments to patients faster than ever. 🚀 #ClinicalTrials #market #regulations #OnlineCourses #SymmetricTraining

Advance Your Expertise in Inhalation Drug Product Development Explore the complexities of developing inhalation drug products in our upcoming online training. Master the latest regulatory guidance and overcome the challenges of characterising various product types (pMDI, DPI, nebulizers). Learn specific methods for APIs and excipients, and receive expert advice on validation and control strategies. Visit our website for full details, check out the LinkedIn event, and register today!

Master the Regulatory Requirements for Drug/Device Combination Products Join our online training to explore the regulatory requirements and navigate the challenges to achieving market authorisation for drug/device combination products. Deepen your understanding of risk and quality management systems, all grounded in the key standards and regulations that shape this field.