SeerPharma’s Post

Excited to share that I have successfully completed the course on 'Introduction to Good Manufacturing Practices (GMP)'! This course provided valuable insights into the standards and regulations that ensure the quality and safety of products in manufacturing. I'm eager to apply these principles in my future work and contribute to maintaining high industry standards. #GMP #ContinuousLearning #QualityControl #ProfessionalGrowth

🖥 Very Happy to share that QbD-Expert™ successfully completed “Quality by Design (#QbD)” Hands-On Online Practical Training Workshop Worldwide during Q3:Q4 2023-24 ! ➕️⌨️ #Feedback from all the participants was #EXCELLENT as "genuinely this was the best DoE | QbD | SPC Practical Training Workshop We've attended ever. Dr. Shivang has simplified entire complex subjects of #DoE #QbD #SPC into directly easy to apply systematic methodology through his creative presentation skills along with Practical #Case_Studies & entire relevant #Course_Materials (Master Guides - Manuals - Templates - Worksheets - Calculators) on almost all the types of Pharma Products & its Mfg Processes". ➕️🖱 #Participation of each participant in all the basic technical modules of QbD/DoE/SPC was #COMMENDABLE which could be felt & observed by their very active dedicated involvement in all the advanced practical case studies during entire practical workshop. 🔝QbD-Expert™ is wholeheartedly thankful to all the participants worldwide across 13+ countries for their very actice participation. QbD-Expert™ ensures that we will be your lifetime partner towards EXCELLENCE !🎖

Proud to share that I’ve completed the Introduction to Good Manufacturing Practices (GMP) course! This experience has strengthened my understanding of quality, compliance, and safety in manufacturing processes. Excited to apply these principles to ensure product safety and efficacy throughout my career! #GMP #ProfessionalGrowth #QualityFirst

We have a lot of really insightful and engaging courses coming up! There is always something new to learn in this industry, so this is a great way to stay on top of things. #Education #Regulatory #Courses

#QualityPioneer William Edwards Deming (October 14, 1900 – December 20, 1993) Edwards Deming was an American engineer, statistician, professor, author, lecturer, and #managementconsultant. Educated initially as an electrical engineer and later specializing in mathematical physics, he helped develop the sampling techniques still used by the U.S. Department of the Census and the Bureau of Labour Statistics. Edwards Deming is considered by many to be the #father of the #total  #quality #management movement. Edwards Deming's theories are based  on the simple concept that continual improvement can help increase  quality while decreasing costs, or what we can call total quality management. Deming’s #14 #Points on Quality Management, or the Deming Model of  Quality Management, a core concept on implementing total quality  management (#TQM), is a set of management practices to help  companies increase their quality and productivity. Deming's #14 #Points for Total Quality Management: I. Create constancy of purpose for improving products and services. II. Adopt the new philosophy. III. Cease dependence on inspection to achieve quality. IV. End the practice of awarding business on price alone; instead, minimize total cost by  working with a single supplier. V. Improve constantly and forever every process for planning, production and service. VI. Institute training on the job. VII. Adopt and institute leadership. VIII. Drive out fear. IX. Break down barriers between staff areas. X. Eliminate slogans, exhortations and targets for the workforce. XI. Eliminate numerical quotas for the workforce and numerical goals for management. XII. Remove barriers that rob people of pride of workmanship and eliminate the annual  rating or merit system. XIII. Institute a vigorous program of education and self-improvement for everyone. XIV. Put everybody in the company to work accomplishing the transformation. #Qualityguru #QualityPioneer #TQM #continuousimprovement  #training #kaizen  #projectmanagement #productivity  #turnkey #greenField #pharmaproject #gmpservices #TQM #QbD #Currentapproach #Pharmaceuticals #GMP #GxP  #pharma #Nutra #pharmaindustry  #regulatorycompliance #regulatoryaffairs  #FDA #WHO #regulation  #gapassessment #siteaudit #GMPAuditors  #drugdevelopment #drugsafety  #APIs #formulations #manufacturingplant #consultants #pharmaconsultant #qxp #qxpgroup

I struggled academically in junior secondary school, particularly with reading comprehension. Reading and comprehending proved to be a difficult course for me, but with brilliant supportive friends surrounding me I began to walk rather than crawl. I recall in JSS 2, out of my friend group, I had a particular friend who took out time to help me prepare for an exam. From this friend, I improved my reading skills and learned valuable techniques like using acronyms to recall important information. This skill has stuck with me, and I'm now a confident reader. In the pharmaceutical industry, acronyms like the 5Ps of Good Manufacturing Practices (GMP) are used from time to time. These 5Ps are crucial for ensuring product quality and consistency. GMP is a comprehensive system that guarantees quality standards throughout a product's lifecycle. The 5Ps stand for: ✍🏼 People: The foundation of a successful GMP implementation. Employees are expected to adhere strictly to the regulations and all production processes. This is ensured by regular GMP training to increase the understanding of their roles, responsibilities, and the importance of their contributions to product quality and safety. Productivity, efficacy and competency can be aided by regular performance assessment. ✍🏼 Products: Clearly defined specifications for all primary materials including raw materials, other components, intermediate and finished products must be available at every production phase. It is essential to adhere to standard methods for manufacturing and packing, testing, sampling, status control, stability studies and records. ✍🏼 Processes: Simple, consistent and properly documented processes should be accessible to all employees. Regular evaluations should be conducted to ensure compliance with the current process and quality standards. ✍🏼 Procedures: A set of guidelines covering all critical processes play a pivotal role in achieving consistent results. Immediate reporting and thorough investigation is done in the occurrence of a deviation from standard procedures. ✍🏼 Premises: It is essential to enhance cleanliness to prevent cross-contamination, accidents or other fatalities. Equipment placement, proper storage, validation and regular calibration are required to ensure their optimal performance thereby producing reliable and consistent results and preventing failure. These components ensure stringent quality control in the pharmaceutical industry. #quality #gmp #5Ps #procedure

Excited to have attended the insightful webinar titled "The Latest Updates in GMP" arranged by IPI Academy Academy. A big thank you to the speaker, Mustafa Edik, for sharing his extensive knowledge and providing us with the latest advancements in Good Manufacturing Practices. The session was incredibly informative and will undoubtedly enhance my understanding and application of GMP standards in my professional journey. Looking forward to more such enriching learning experiences! #GMP #ProfessionalDevelopment #IPIacademy #Webinar #ContinuousLearning

🚀 Boost Your Manufacturing Skills with our Manufacturing course! Learn the fundamentals of Lean principles and Good Manufacturing Practice (GMP) to streamline processes, reduce waste, and improve quality. Perfect for anyone looking to level up in the manufacturing industry! 🔧 🔹 Understand Lean techniques for efficiency 🔹 Master GMP 🔹 Applicable to all industries Sign up today! https://lnkd.in/eiSuu3h3 #LeanManufacturing #GMP #ManufacturingExcellence #SkillsDevelopment #ContinuousImprovement

🌟 Join Our Web-Seminar: Declaration of Compliance (DoC) and Good Manufacturing Practice (GMP) for Food Contact Materials (FCM) 🌟 📅 Date: November 12, 2024 🕑 Time: 14:00 - 17:00 CET 💻 Language: English 👨🏫 Facilitator: Dr. Ioan Paraschiv, Knoell NL B.V. 💰 Fee: €350.00 plus legal VAT Are you a Regulatory Affairs Manager or a Product Stewardship Specialist in the food contact supply chain? Enhance your expertise with our comprehensive 3-hour web-seminar focused on GMP and DoC for FCMs. 📚 What You'll Learn: ✔️The GMP Regulations and requirements applicable to all industry sectors and all stages of manufacture, processing and distribution of FCMs in markets such as the EU, Switzerland, US, Canada, China, Mercosur countries and Japan ✔️The steps to be considered in implementing a quality assurance system and policies for FCMs ✔️How to implement a hygiene policy, where applicable ✔️The steps with respect to documentation, labelling, document retention and traceability of FCMs ✔️How to address the key aspects of the FCM production process, including: raw material specifications, contamination prevention, management of change, storage packaging, warehousing and transportation ✔️How to carry out quality control and check specifications for FCMs ✔️How to outsource work under GMP for FCMs ✔️How to handle a compliance complaint, a product recall, and incident management for FCMs ✔️How to perform regular internal and supplier (external) audits for FCMs 🔍 Who Should Attend: This seminar is tailored for professionals involved in regulatory compliance and product stewardship within the food contact materials sector. Don’t miss this opportunity to deepen your understanding and stay compliant in a rapidly evolving regulatory landscape. 👉 Find out more and register here: https://ow.ly/Gj0H50TqXbB #GMP #FoodContactMaterials #RegulatoryAffairs #WebSeminar #QualityAssurance #Compliance #FCM #FoodSafety #ProfessionalDevelopment

Come join me and my Yordas colleagues who are passionate about helping you understand the complex #regulatory obligations you may face