AGON

What do our #clients and #partners think of #Agon‘s #services and #trainings? Watch this #testimonial video to find out more! 👇

We are absolutely thrilled to announce and share photos from our collaboration with SAJA Pharmaceuticals Company, where we successfully launched our very first SFDA Qualified Person training programs! The program featured two essential sessions: "Data Integrity" and "Root Cause Analysis & Handling of Deviation" held at the esteemed Tamer Academy in Jeddah | KSA These sessions were a tremendous success, equipping pharmaceutical professionals with the critical skills and knowledge needed to excel in their fields and ensure compliance with SFDA regulations It was a fantastic opportunity for attendees to network, learn from industry experts, and enhance their professional credentials Stay tuned for more updates on our upcoming QP training sessions, exciting details, and additional resources that will help you stay at the forefront of the pharmaceutical industry!  Register Here:  https://lnkd.in/ePcyNWCr #PharmaceuticalTraining #DataIntegrity #RootCauseAnalysis #SFDAQualifiedPerson #TamerAcademy #Jeddah #KSA #ProfessionalDevelopment #PharmaExcellence #IndustryLeadership #ContinuousImprovement

عام هجري مبارك نسأل الله أن يجعله عام خير وبركة، مليء بالنجاحات والسعادة لكم ولأحبائكم 🤲 #عام_هجري_مبارك #السنة_الهجرية_الجديدة #تمنياتنا_بالخير

Reflecting on our experience at the 6th Arab Pharma Manufacturers’ Expo 2024! 🌍 It was an enriching event filled with insightful sessions, valuable networking, and cutting-edge innovations in pharmaceutical manufacturing ✨ 📅 Date: July 2-3, 2024 📍 Venue: Jordan International Exhibition Center (JIEC) Amman - Jordan #AgonPharma #ArabPharmaExpo #PharmaInnovation

Join us for a comprehensive 2-day training on the Basics of Analytical Testing & Basics of Analytical Method Validation! 🌟 📅 Date: August 6-7, 2024 📍 Location: Tamer Academy, Jeddah, KSA Don't miss this chance to enhance your skills and knowledge in analytical testing and method validation. Perfect for professionals seeking to stay ahead in the pharmaceutical industry! 🔗 Register now and secure your spot! https://lnkd.in/ecbFTYjh #Training #Pharma #AnalyticalTesting #MethodValidation #ProfessionalDevelopment #TamerAcademy #Jeddah #KSA

As part of our unwavering commitment to maintaining the highest standards in our pharmaceutical manufacturing processes, we would like to highlight some key challenges we face in cleaning validation and propose effective solutions to address them 🌟 Challenges and Solutions 🔧 Complex Equipment Design : ⚠️ Challenge: The intricate design of some manufacturing equipment can make thorough cleaning a daunting task. ✅ Solution: Implementing Clean-In-Place (CIP) systems can greatly simplify the cleaning process for complex equipment. CIP systems are designed to clean the interior surfaces of pipes, vessels, process equipment, and associated fittings without disassembly, ensuring consistent and efficient cleaning. 🔬 Analytical Method Development: ⚠️ Challenge: Detecting low levels of residues requires highly sensitive and specific analytical methods. ✅ Solution: It is imperative to invest in robust and advanced analytical methods. Techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC) can provide the necessary sensitivity and specificity to detect even trace amounts of residues, ensuring that our cleaning processes meet stringent quality standards. 📜 Regulatory Changes: ⚠️ Challenge: The regulatory landscape is constantly evolving, with new guidelines and requirements emerging regularly. ✅ Solution: To stay compliant, we must proactively keep abreast of regulatory updates and integrate them into our cleaning validation protocols. This involves regular review and updates to our standard operating procedures (SOPs) and continuous training for our staff on the latest regulatory requirements. By addressing these challenges head-on with effective solutions, we can enhance our cleaning validation processes, ensuring product safety and compliance with regulatory standards. For more info, contact us! 📩 [email protected] 📱 962 7 9153 3337 #KSA #iraq #challenges #cleaning #validation #ccs #cv

Key Elements of Contamination Control Strategy in the Pharmaceutical Industry  Facility Design and Layout: Cleanroom Classifications:  Design facilities with cleanrooms that adhere to specific classifications (ISO 14644-1) to control particulate contamination. Airflow Patterns: Utilize unidirectional airflow and high-efficiency particulate air (HEPA) filtration systems to prevent airborne contaminants. Segregation of Areas: Create dedicated areas for different stages of production (e.g., raw material handling, formulation, packaging) to minimize cross-contamination.  Personnel Hygiene and Training: Gowning Procedures: Enforce strict gowning procedures, including wearing appropriate protective clothing to reduce the risk of contamination. Training Programs: Conduct regular training on contamination control practices, including proper hand hygiene, gowning techniques, and behavior in cleanrooms.  Equipment and Material Controls: Sterilization and Disinfection: Perform regular sterilization of equipment and disinfection of surfaces to prevent microbial contamination. Material Handling: Use closed systems and barriers to protect materials from environmental contamination during transfer and storage.  Environmental Monitoring: Air Quality Monitoring: Continuously monitor airborne particulates and microorganisms in cleanrooms using air samplers and settle plates. Surface Monitoring: Routinely sample surfaces (e.g., workbenches, equipment) to detect and control microbial contamination. Personnel Monitoring: Regularly monitor personnel for contamination, including gown and glove sampling.  Process Controls: Aseptic Processing: Implement aseptic techniques during the manufacturing of sterile products to prevent contamination. Validated Cleaning Procedures: Use validated cleaning and sanitization procedures for equipment and facilities. Environmental Control Systems: Install HVAC systems to maintain controlled temperature, humidity, and pressure differentials.  Quality Control and Assurance: Good Manufacturing Practices (GMP): Adhere to GMP guidelines to ensure the consistent quality of pharmaceutical products. Risk Assessment: Conduct regular risk assessments to identify potential sources of contamination and implement corrective actions. Documentation and Record-Keeping: Maintain detailed records of all contamination control activities for traceability and regulatory compliance. Avoid Contamination! Contact us: [email protected]   962 7 9153 3337 #ccs #agon #control #Contamination #jordan #ksa #iraq #oman

Ensuring Trust Through Data Integrity 💻💡 At Agon, we understand that data integrity is crucial in maintaining the highest standards of quality and safety in the pharmaceutical industry 💊 Our comprehensive Data Integrity services are designed to help your company achieve and maintain regulatory compliance with FDA, EMA, and WHO standards🥇 🔍 What We Offer: ✅ Thorough data integrity assessments ✅ Robust documentation and record-keeping solutions ✅ Comprehensive training for your team ✅ Implementation of advanced access controls ✅ Detailed audit trails for complete transparency 📞 Contact us now to learn more about our services and how we can help you maintain the highest standards of data integrity. [email protected] 962 7 9153 3337 #Pharmaceuticals #DataIntegrity #Compliance #QualityAssurance #AgonConsulting #FDA #EMA #WHO #PharmaSafety #PharmaQuality #PharmaConsulting

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Eid Al Adha Mubarak 🌙 Eid Al Adha is a time for reflection, gratitude, and compassion, this year, our hearts are heavy with the ongoing conflict in Gaza and Sudan, and we stand in solidarity with all those affected. May this Eid bring strength and hope to all the beautiful souls are suffering 🕊️