Project Farma (PF)’s Post

I love to see these posts about our Professional MS graduates who are thriving in their careers after graduation! Davidson School of Chemical Engineering Professional Master's Program

Thermal runaway incidents continue to occur in batch production facilities in the chemical and pharmaceutical industries. Serious incidents can result in death, injury, capital loss, and business interruptions. Prior to scale-up, it is critical to have a clear understanding of the reactivity of all process chemicals as well as the energetics of both desired and undesired reactions, identify a worst-case scenario, characterize the resulting adverse reaction, and understand how to mitigate the process safety impact. #ProcessSafety #ChemicalIndustry #PharmaceuticalIndustry #SafetyManagement #RiskPrevention #SafetyCulture #IncidentPrevention #ReactivityAnalysis #SafetyStandards #RiskMitigation #HazardousMaterials

🔬Compliance Process Step 1: Document Submission 🔬 The journey to regulatory compliance starts here! At COSICHEM, we simplify the process for you. The first step is submitting the right documents. These documents form the foundation for our thorough chemical review, ensuring your product adheres to European safety and regulatory standards. For a list of required documents, please contact us. Once we receive everything, our team of experts gets to work, analyzing each component to ensure compliance. With COSICHEM, you can trust that every chemical detail is handled professionally. 🧪🔍 #ChemistryIndustry #ChemicalRegulations #SDS #DocumentSubmission #ChemicalCompliance #RegulatoryExperts #ProductSafety #EUCompliance #ComplianceProcess #ChemicalSafety

Our fire safety solutions are designed to enhance the safety across diverse industries like pharmaceutical, biomedical, and biotechnology. Uniqueness of these industries leads them to face unique fire risks in their chemical facilities, clean rooms, labs, warehouses, and electrical systems. Leveraging advanced technology, customized specifically for the industry, our innovative solutions swiftly and effectively detect and control fires, safeguarding lives, property and maintaining business continuity. Join our exclusive session on Fire Safety in Pharma Industry and learn about the latest codes and standards designed for the industry. Enhance your expertise in ensuring safety and operational resilience. Understanding Fire Safety at Pharmaceutical Facilities Considering the distinct characteristics of the pharmaceutical industry, it is crucial to safeguard essential areas within the facilities to ensure continuous fire safety. Honeywell's advanced fire safety systems offer pharmaceutical companies unmatched protection in their regulated environments, with adaptable, reliable and efficient solutions to ensure rapid response and minimal disruption during fire incidents. What’s in it for you? Ensure Compliance: Learn how to navigate the complex landscape of fire safety regulations. Stay Ahead: Keep up-to-date with the latest advancements and regulatory requirements. Enhanced Safety Protocols: Learn how to implement and maintain robust safety measures. Operational Integrity: Understand how to design and enforce fire safety plans for safe operations. #Mandar Sawant#Protyush Debnath#Ruchika Singh#U Rajesh Rao#Kamal Joshi#Nitin Singla#Sandeep Patil https://lnkd.in/gJNFuC64

From monitoring critical processes in the pharmaceutical industry to controlling and monitoring all IAQ parameters: Automated environmental monitoring saves resources and offers clear benefits for sensitive sectors such as hospitals, laboratories, the food industry and in the manufacture and storage of chemicals. Many companies still use manual recording methods or mobile data loggers, which takes up to 20% of employees' working time and involves security issues. In contrast, automated monitoring ensures continuous quality assurance and increases reliability both internally and for end customers. ️🌡️🔍 Testo places great value on comprehensive customer support from start to finish, including project planning, commissioning, maintenance and calibration as well as qualification and validation. One outstanding example of this is the internationally active laboratory supplies specialist Carl Roth. The company has been using the innovative environmental monitoring system since 2020: Here, the system is primarily used for temperature monitoring in the production and storage areas. Find out more here: https://lnkd.in/dajYNMfH  This advanced technology not only enables efficient resource savings, but also facilitates audits, resulting in optimized overall performance and higher customer satisfaction. #environmentalmonitoring #temperaturemonitoring #temperaturemeasurement #besure

🚨 Product failed a compliance check? Don’t panic! In this reel, we walk you through the step-by-step actions you should take if your product doesn't meet regulatory standards. From reviewing the safety report to correcting labels, there are ways to fix issues and get your product back on track for market approval. ✔️ At COSICHEM, we help identify the problem areas and offer expert solutions to ensure your product passes the next round of checks. 📞 Need help? Contact our experts today! #ComplianceCheck #ProductCompliance #COSICHEM #FailedCompliance #RegulatorySupport #FixComplianceIssues #MarketReady #CosmeticCompliance #GetBackOnTrack #ExpertSolutions

SOLWEYA Engineering Quality and compliance, guaranteed. Trust our validation experts! #PharmaValidation #ProductExcellence #IndustryStandards #BioPharmaValidation #QualityAssurance #ValidationExperts #GMPCompliance #PharmaQuality #ExceedExpectations #ValidationSolutions

VALIDATION AND QUALIFICATION OF WATER PURIFICATION,STORAGE,AND DISTRIBUTION SYSTEMS Establishing the dependability of pharmaceutical water purification,storage,and distribution systems requires an appropriate period of monitoring and observation.Ordinarily,few problems are encountered in maintaining the chemical purity of Purified Water and Water for Injection.However,it is more difficult to meet established microbiological quality criteria consistently.Atypical program involves intensive daily sampling and testing of major process points for at least one month after operational criteria have been established for each sampling point. Validation is the procedure for acquiring and documenting substantiation to a high level of assurance that a specific process will consistently produce a product conforming to an established set of quality attributes.The validation defines the critical process parameters and their operating ranges.Avalidation program qualifies the design,installation,operation,and performance of equipment.It begins when the system is defined and moves through several stages:qualification of the installation (IQ),operational qualification (OQ),and performance qualification (PQ).Agraphical representation of a typical water system validation life cycle is shown in Fig.1. Fig.1.Water System Validation Life Cycle #WaterValidation 💧 #WaterQuality 🌊 #WaterTesting 🔬 #WaterSafety 🚰 #CleanWater 💦 #WaterStandards 📏 #WaterAnalysis 🧪 #EnvironmentalMonitoring 🌍 #WaterTreatment 🛠️ #WaterConservation 🌱 #WaterIntegrity 🛡️ #SafeDrinkingWater 🥤 #WaterResearch 🔍 #WaterScience 🔬 #WaterQualityTesting 📊 #USP1231

ENVIRONMENT MONITORING PROCEDURE IN PHARMA Environmental monitoring (EM) is a critical process in the pharmaceutical industry that ensures the quality of controlled environments For Detail Click Below: https://lnkd.in/gsB-cyS5

Our latest edition of the Tried & Blue blog is here! Dive into the detailed process of building a top-notch cGMP environment with insights from our Program Development Manager. Want to learn how we navigate the intricacies of constructing these types of facilities? Check out the full blog post now! #BuildingsStandWithErland