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𝐃𝐞𝐥𝐩𝐡𝐚𝐫𝐦 𝐀𝐜𝐚𝐝𝐞𝐦𝐲 𝐬𝐚𝐭𝐢𝐬𝐟𝐢𝐞𝐬 𝐭𝐡𝐞 𝐆𝐫𝐨𝐮𝐩'𝐬 𝐞𝐦𝐩𝐥𝐨𝐲𝐞𝐞𝐬: "𝐀𝐧 𝐞𝐬𝐬𝐞𝐧𝐭𝐢𝐚𝐥 𝐩𝐫𝐨𝐜𝐞𝐬𝐬 𝐟𝐨𝐫 𝐃𝐞𝐥𝐩𝐡𝐚𝐫𝐦”
Since the beginning of 2024, Delpharm employees who had completed face-to-face training rated a global satisfaction rate of 4.7/5.
𝑊ℎ𝑎𝑡 𝑚𝑎𝑘𝑒𝑠 𝑡ℎ𝑒 𝐷𝑒𝑙𝑝ℎ𝑎𝑟𝑚 𝐴𝑐𝑎𝑑𝑒𝑚𝑦 𝑑𝑖𝑓𝑓𝑒𝑟𝑒𝑛𝑡?
During training sessions, participants have the opportunity to exchange and meet colleagues from other site and to follow training tailored to their needs.
#humanresources#Delpharm#pharmaceuticals
Hi Ashwini Deshpande, 𝗖𝗼𝗻𝗴𝗿𝗮𝘁𝘂𝗹𝗮𝘁𝗶𝗼𝗻𝘀, 𝗮𝗻𝗱 𝘄𝗲𝗹𝗹 𝗱𝗼𝗻𝗲 𝗼𝗻 𝘁𝗵𝗶𝘀. Ashwini covered the following areas on this programme:
- Introduction – to pharmaceutical, (bio)pharmaceutical manufacturing in a GMP (Good Manufacturing Practice) regulated environment, quality systems, regulation and validation
- Industry regulations and guidelines for GMPs – including, FDA GMPs for the United States, EMA GMPs for European Union, ICH, and PICs GMP regulation
- FDA medical device rules – medical device regulations & and guidelines
- GMPs vs ISO 9001:2015 – what’s the difference and why we use both
- Process validation and documentation – design and verification of manufacturing systems
- Key manufacturing technologies – such as organic chemical synthesis, biopharmaceutical manufacturing, tablet manufacturing and aseptic and sterile manufacturing
- Supporting technologies – such as purified water generation, storage and distribution, clean steam, water for injection, storage and distribution
- Introduction to Quality Risk Management (QRM) – and the importance of risk management and the basic steps involved in its application
- Working in a cleanroom environment – layout, classification, gowning and monitoring
- Professional Writing Skills Program – This will guide you through the assignment writing process and equip you with the written communication skills you need for working in the industry
For an end-of-module assignment, Ashwini completed a 1200-word report on the cGMPs that are required to consistently manufacture safe medicines, vaccines and medical devices for patients.
It included:
- The key requirements of a quality management system
- The cleaning validation sequence and how to determine cleanliness levels
- The documentation of a complete risk management process in terms of identifying risk, analyzing risk, evaluating risk and controlling risk.
- The typical equipment and process stages used in the manufacture of active pharmaceutical ingredients
- The generation, storage and distribution of pharmacopoeia grade Purified Water (PUW).
- The common cleanroom configuration and airflow direction that governs personnel and material flows in a biopharmaceutical manufacturing environment
Well done again.
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Learn more by checking out this course on the LearnGxP website, or book a demo with our experts: https://lnkd.in/e-2mXjuE#GMP#Pharmaceuticals#AnnualRefresherTraining#GxP 🚀
Pharm-D Student | Hamdard university |Dedicated Healthcare Professional | Hospital & Clinical Experience | Seeking Opportunities in pharmaceutical industry |
🎉 Excited to share that I've successfully completed the "Introduction to Good Manufacturing Practices (GMP)" course with Pharmuni ! 🏆 This achievement is a significant step in my journey towards ensuring the highest standards in the pharmaceutical industry. 💊
Staying updated with industry standards is crucial, and this certification is a testament to my dedication to quality and excellence. 🌟
I'm eager to apply these best practices in my work and contribute to the safety and efficacy of our products! 🚀
#ContinuousLearning#Pharmaceuticals#GMP#ProfessionalDevelopment
I am pleased to share that I have recently completed the Good Manufacturing Practice (GMP) in Pharmaceutical Industry course with PharmaState Academy. This certification has enriched my expertise in the stringent protocols and quality benchmarks that are the cornerstone of pharmaceutical integrity.This journey has been an illuminating exploration into the meticulous processes that ensure the safety, purity, and efficacy of the medicines we trust. As I continue to cultivate my knowledge, I am inspired to contribute meaningfully to the pharmaceutical landscape, guided by the principles of excellence and precision.
#PharmaState#GMPStandards
Aspiring Pharmaceutical Technologist || B.Pharm || Six Sigma White Belt || CRM ||Good Clinical Practices(GCP) || Campus Ambassadors || Aspire Leader by Harvard Business School || AI || Digital marketing ||
Pursuing B. Pharmacy at ICPR | Learning Medical Coding at HCV | Ex - Intern at BSES MG Hospital |
Ex - Drug Analyst Intern at FDA | Dedicated to Healthcare and Technology
I am thrilled to share that I have completed the comprehensive CDSCO course offered by PharmaState Academy. This program has equipped me with in-depth knowledge of the Central Drugs Standard Control Organization (CDSCO) and its regulatory framework, empowering me in the dynamic pharmaceutical landscape.
Throughout the course, I delved into critical aspects of drug regulation, compliance, and the latest updates in the pharmaceutical industry. The practical insights and real-world scenarios provided by PharmaState Academy have been invaluable, enhancing my understanding and proficiency in this critical field.
#CDSCO#PharmastateAcademy#Pharmaceuticals#RegulatoryCompliance
Pharma Compliance Rx is excited to announce our participation in CPhI Milan, the premier global event for the pharmaceutical industry. Meet us in Italy to explore our cutting-edge GxP audit and compliance solutions, tailored to help businesses navigate the complexities of regulatory requirements across North America, Europe, India, and China. Let’s discuss how we can support your company’s growth and compliance needs.
See you there!
#CPhIMilan#PharmaCompliance#GxPCompliance#RegulatorySolutions#PharmaceuticalIndustry#GlobalCompliance#Milan2024
🐼 Bravo aux équipes et aux élus du CSE qui ouvrent chaque jour pour les collaborateurs 👏🏽💡