SEN Pharma

✍ Sun Pharma: A Global Healthcare Leader Sun Pharmaceutical Industries Ltd (Sun Pharma), a leading multinational pharmaceutical company, is making headlines with a significant initiative: a tourism-related business trip to Vietnam for 4,500 employees. This move underscores Sun Pharma's commitment to employee well-being and its robust financial position in the global healthcare market. ✨ Founded in 1983 by billionaire Dilip Shanghvi, Sun Pharma has rapidly expanded its operations to over 100 countries and acquired prominent subsidiaries like Ranbaxy Laboratories. Renowned for its high-quality and affordable products in dermatology, oncology, and ophthalmology, Sun Pharma's success can be attributed to strategic acquisitions, global expansion, substantial investments in research and development, and a diverse product portfolio. 👉 For more interesting facts about this Company, please visit: https://lnkd.in/gm_WDQeM

✍ Who is the Person in charge of Ensuring the Quality, Safety, and Efficacy of Pharmaceutical Products when Releasing ? ❓ Have you ever wondered who is responsible for ensuring that the pharmaceutical products you and your family use are of the highest quality? ❓ As a professional in the pharmaceutical industry, have you ever heard of a Qualified Person (QP)? 💡 In the European pharmaceutical sector, a Qualified Person (QP) is a highly skilled individual with legal responsibility for the quality, safety, and efficacy of pharmaceutical products manufactured or imported into the European market. ⁉ Why are QPs important? ⚜ QPs act as the final safety net, ensuring that only safe and effective pharmaceutical products reach the market. Their presence safeguards public health and maintains the reputation of the pharmaceutical industry. In essence, a Qualified Person is a critical role in the European pharmaceutical industry, dedicated to ensuring the quality, safety, and efficacy of pharmaceutical products for the benefit of public health. 🔥 Want to learn more about Qualified Persons or the pharmaceutical industry? 🔥 Join our QA-07: Quality Control & GLP - Qualified Person course offered by SEN Pharma! 👉 For more details and to enroll, please visit the link:  https://lnkd.in/gGcsFmPR  

✍ Unveiling the Pharmaceutical Giants: Top 20 Companies of 2023 👀 Ever wondered who's leading the charge in the world of pharmaceuticals? Dive into the exciting world of the top 20 global pharmaceutical companies of 2023! Discover which giants dominate the industry, what drove their success, and what trends are shaping the future of medicine. 👉 Here is the overview of the top 20 global pharmaceutical companies based on their 2023 revenue. Key Findings: 🥇 The pharmaceutical industry experienced robust growth in 2023, with Johnson & Johnson leading the pack at $85 billion. 🥈 Companies like Merck & Co. and AbbVie showcased strong performances, while Pfizer saw a decline due to reduced COVID-19 product demand. 🥉 Strategic acquisitions and divestitures were prevalent, with companies focusing on expanding portfolios and optimizing operations. 🎖 Innovation in areas like oncology, diabetes, and specialty drugs remains a key focus for continued growth. 👉 Full details and company-specific insights can be found here: https://lnkd.in/g73Bumzk  

🔥 GLP: A Cornerstone of global - GMP Compliance 🔥 Adherence to Good Laboratory Practice (GLP) is a non-negotiable requirement for any pharmaceutical manufacturing facility aiming to achieve GMP certification. GLP ensures that quality testing and inspections are conducted accurately and transparently, providing the foundation for robust data integrity. ⁉ How can you ensure your Quality Control laboratory is consistently GLP-compliant? 💡 Join SEN Pharma's QA-07: Quality Control & GLP - Qualified Person course! This comprehensive program will delve into the significance of GLP, the specific requirements of GMP, and how to effectively establish and maintain a GLP system within your QC department. Under the guidance of Dr. Edward Balbirnie, a seasoned EU Qualified Person with over 30 years of international experience, you'll gain both theoretical knowledge and practical insights to implement GLP in your manufacturing processes, enhancing product quality and bolstering your company's reputation. 🔎 Don't miss this opportunity to: 📜 Update your knowledge on the latest GLP standards. 📝 Ensure your facility is ready to meet stringent international requirements. 🎁 Benefit from a 20% discount for the first 20 registrants. 👉 For more details and to register, please visit the link: https://lnkd.in/gGcsFmPR

💎 💎 💎 Are you a pharmaceutical company seeking to introduce your innovative drugs to the European market? EU drug registration can be a complex process, demanding strict adherence to quality and safety standards set by the European Medicines Agency (EMA). This comprehensive overview helps you to delve into the essential stages of the drug registration process, providing valuable insights for pharmaceutical companies seeking to introduce their products into the European market. 🔥 Ready to Launch Your Drugs in Europe, but still unsure where to start ? 👉 SEN Pharma can offer trusted guidance throughout your EU drug registration journey. 👉 Read full article here: https://lnkd.in/gqBVmTBF

🤔 💢 Are you tired of dealing with OOS and OOT? Out of Specification (OOS) and Out of Trend (OOT) results can be a major headache in pharmaceutical manufacturing. These findings not only disrupt production but also put product quality and patient safety at risk. 🔥 When faced with OOS/OOT, how do you proceed? 🔥 How can you quickly identify root causes? 🔥 What tools can help you investigate effectively? 🔥 And how do you implement corrective actions and preventive action? 💡 Don't worry! All your questions will be answered in our QA-07 course- Module 5: Quality Control & GLP - Qualified Person, led by Dr. Edward Balbirnie, a seasoned quality expert with over 30 years of international experience. You'll gain the essential skills to effectively handle and prevent OOS and OOT. 🔎 Register now and take control of your quality processes. 👉 Find more information here: https://lnkd.in/gGcsFmPR 👉 Link to registration: https://lnkd.in/g6TS7vds

👀 How can an EU-GMP certified facility register a drug in Europe? Obtaining EU drug approval is a rigorous process that demands meticulous adherence to the EMA's or national regulatory authorities' regulations. ⁉ Have you get the clear roadmap for EU drug registration yet ? 🔥 This process can be intricate, but with the right guidance, your EU-GMP certified facility can navigate it successfully. ✍ Key Steps for EU Drug Registration: 1.    Data Preparation: including preclinical & clinical data, CMC (chemistry, manufacturing and controls) data 2.    Choosing the Registration Pathway: There are four main procedures for drug registration in the EU following EU-GMP standards 👉 For a more detailed information and explanation of each registration procedure, please refer to the full article here: https://lnkd.in/gp7YC7yS

🤝 Communication is a cornerstone of success, both in work and life. 👀 But how do we handle the inevitable bumps in the road, like negative feedback? 🎖 SEN Pharma belives that by mastering key strategies to navigate criticism, you can transform negative feedback into a catalyst for personal and professional development. Ready to unlock your full potential? Read SEN Pharma's article and discover the power of transforming negative feedback into fuel for your success! 👉 Click here to get started: https://lnkd.in/enevYw7y

✨ INTRODUCING OF IN-DEPTH TRAINING COURSE "QA-07 - MODULE 5: Quality Control & GLP – Qualified Person (QP)” ✨ 🎁 Special 20% discount for the first 20 registered students (Individual registration) 🎁 Do you want to master the knowledge of quality control and good laboratory practice (GLP) complying with international standards? Do you want to become a Qualified Person (QP) with internationally recognized knowledge and skills? 🎗 Join the course “QA-07– Module 5: Quality Control & GLP - Qualified Person (QP)” with SEN Pharma! 🎗 Learn from Dr. Edward Balbirnie, a renowned EU Qualified Person with over 30 years of international experience, participants will be equipped with core knowledge and sharp thinking in quality control. 👉 Let's explore the detailed information of the course with SEN Pharma in the article: https://lnkd.in/gGcsFmPR Hurry up and register to become one of the first 20 participants to receive a special offer! Don't miss the opportunity to improve your professional skills and expand your career! 👉 Register now at https://lnkd.in/geUEMRmM 🔥 SEN Pharma - Accompanying you on the journey to improve your quality system. 🔥

✍ Unlocking the Power of Computerized Systems: CSV Solutions In today's fast-paced pharmaceutical landscape, computerized systems are essential for streamlining operations and ensuring product quality. However, implementing Computerized System Validation (CSV) can be a daunting task, especially for companies facing: ⚡ Legacy system upgrades: Migrating to modern systems while maintaining compliance. ⚡ Integration challenges: Integrating diverse software solutions seamlessly. ⚡ Technical expertise gaps: Addressing the lack of in-house knowledge. ⚡ Resource constraints: Balancing CSV efforts with other operational demands. ⁉ What SEN Pharma can help ? At SEN Pharma, we understand the unique challenges you face and offer tailored CSV solutions to help you overcome them. Our partnership with FactoryTalk, a global leader in CSV, provides access to a team of seasoned experts with over 18 years of experience. 💪 Ready to Take Control of Your Computerized Systems? Contact SEN Pharma today for a consultation. 👉 Read full article to know more about our comprehensive services: https://lnkd.in/giCk749J