TetraScience’s Post

Unlocking the Power of Statistical Insights in Pharmaceutical Quality: Join us for the 3rd Edition of Statistics for Quality Control and Quality Assurance Practice led by renowned expert Dr. Joachim Ermer. Discover the latest advancements in analytical procedure development and gain essential skills to ensure compliance with regulatory standards. 📩 Limited seats available! Reach out now at [email protected] or call us at 1 657 452 8174. Registration link - https://lnkd.in/gb_g9G73 #PharmaceuticalQuality #StatisticalAnalysis #QualityAssurance #QualityControl #ICHGuidelines #AnalyticalProcedures

🔬 𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫 𝐏𝐫𝐨𝐜𝐞𝐬𝐬 𝐕𝐚𝐥𝐢𝐝𝐚𝐭𝐢𝐨𝐧 𝐢𝐧 𝐏𝐡𝐚𝐫𝐦𝐚 🔬 Ever wondered how we ensure every medicine is safe and effective? 🤔 Our latest blog makes it clear! It's all about process validation in pharmaceutical manufacturing. This crucial step guarantees every drug meets top quality and safety standards. 🌟 We break it down simply: what it is, why it matters, and how tech like AI helps. Perfect for both experts and beginners in the field! 👉 Check it out and learn something new today: [Process Validation for Pharmaceutical Manufacturers: Ensuring Quality and Compliance] https://lnkd.in/g2Pnsz4Y #PharmaQuality #SafetyFirst #HealthTech 🚀🧬

In this talk, an approach consisting of a digital loop is presented, leveraging ICH Q9(R1) and ICH Q13 regulatory packages, integrating process data acquisition (via Continued Process Verification plan, for example) and Quality Risk Management systems. This retrofitting digital loop, rooted within the company’s Pharmaceutical Quality System, will enable companies to dynamically refine process control strategies supported by process insights and data, which are then incorporated in a pre-defined formal structure; thus, enabling the expected formal flexibility and reducing subjectivity for quality decisions, both critical concepts for efficient CM processes and safety and efficacy of the final product. Maria Batalha Kevin Bittorf Matthew Mollan John Nadzam #INTERPHEX24

Missed our webinar with Charles River Laboratories on microbial identification technologies in the pharmaceutical industry? Not to worry! 💡This popular webinar is now available on demand! Catch up on all the action and discover the pivotal role of microbial identification in fortifying contamination control strategies within pharma. 🔬 Featuring industry expert Doug Botkin, PhD, this webinar focuses on the complexities of microbial identification technologies and their impact on ensuring product safety and quality. Watch the webinar now: https://bit.ly/441iXIh #pharmaindustry #microbialIdentification #contaminationcontrol #webinar #ondemand #CharlesRiver #qualityassurance #productsafety

🔍 Are you looking to streamline your SOP creation process in the pharmaceutical industry? 🚀 Discover the power of AI in crafting precise Standard Operating Procedures (SOPs) for the pharma industry! With AI's assistance, SOP preparation becomes faster, more accurate, and adaptable to evolving regulations. Embrace the future of pharma documentation. #SOP #AI #PharmaIndustry #Innovation 💡🔬 #PharmaInnovation #AIinPharma #SOPAutomation

Navigating the regulatory landscape for the mandatory Annual Product Quality Review (APQR) can be challenging for pharma companies. BIOVIA's Structured Document Authoring – APQR solution streamlines the complex process of document authoring by offering key advantages: ✅ optimizes regulatory compliance ✅ reduces costs associated with APQR generation ✅ expedites time-to-market for pharmaceutical products The unified platform connects stakeholders, enabling collaboration and proactive issue management. Learn how to enhance APQR compliance, download the datasheet: http://go.3ds.com/sH3.

Traditional pharmaceutical development pathways can be lengthy and expensive, with product performance not fully understood until late in the development cycle. BDD offers an alternative to the traditional model through BDD Swift - an adaptive clinical trial design that integrates formulation development, GMP manufacturing, and clinical testing into one streamlined service. This enables product performance optimization in real time using continuous, rapid feedback from real clinical results. Why have I attached a picture of a chameleon? Because, like BDD, it embodies the essence of adapting to change with agility and insight. Take inspiration from the natural world and embrace the innovative BDD approach! Stop by our booth at the Clinical Trials Innovation Programme (CTIP) on February 20-21 to learn more! #formulationdevelopment #adaptivetrials #manufacturing

I'll be contributing to the upcoming webinar on Pharmaceutical Quality System (PQS) - join us for a discussion. #qualitysystem #pharmaceuticals #regulations #bestpractices

The rapid and accurate identification of microbial contaminants is crucial for quality control in pharmaceutical processes and products. Using genotypic identification methods offer robust and high throughput with simplified testing.   Read on to learn more about how genotypic workflows can help accurately identify thousands of species of microbials as well as provide researchers with confidence in quality control.   https://lnkd.in/g5mktfaK   #bioprocessing #microbialID #microbialtesting #impuritytesting #qualitycontrol #regulatorycontrol #regulatorycompliance