knoell’s Post

🌟 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

🚀 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

Are you new to learning about GMP? Does your factory already have GMP? Do you know that any factory owner wishing to apply for Malaysia Halal certification needs to have GMP first? Let's watch this video to learn more about the importance of GMP for company owners and users.

The Five Ps of #GMP: Quality from every angle Good Manufacturing Practice (GMP) thrives on five pillars: Products, People, Processes, Procedures, and Premises. Each P is a cornerstone of quality in life sciences, ensuring compliance, efficiency, and safety at every step. Let’s spill the (quality-assured) tea on the Five Ps that make GMP tick: 🔬 Products: Quality starts with raw materials and ends with precision in every formula. 🪪 People: Well-trained individuals drive GMP success—training isn’t optional; it’s essential. 🔄 Processes: Meticulously documented processes ensure consistency and compliance. 📖 Procedures: Clear, current guidelines are the roadmap to success. 🏢 Premises: Spotless facilities and well-maintained equipment protect patients and products alike. Sounds simple? It’s not. Staying compliant while scaling excellence isn’t a one-person show—it’s a team sport powered by the right tools. That’s where an #eQMS steps in. In the complex landscape of Good Manufacturing Practices (GMP), companies are continually seeking strategies to streamline their processes and bolster #compliance. With an eQMS, managing GMP becomes second nature. From training reminders to seamless documentation, it’s your all-star teammate for automating, simplifying, and owning the Five Ps. Dive into our latest blog to see how it all connects >> https://bit.ly/3PUb9AC #QualityManagement #QualityCompliance

Good Manufacturing Practice (GMP). Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. #GMP #Good_Manufacturing_Practice #FoodـSafety

In a sector where safety is paramount, ISO 13485 is crucial for ensuring that medical devides are safe and effective.

Supplier quality can make or break your product's integrity. Discover strategies for managing supplier risks and ensuring GMP compliance in our comprehensive blog on Good Manufacturing Practice! #GMPCompliance #ManufacturingStandards

The speed limit is 25, 45, 75… We all know the law. Why then do we speed? Because for however long, it’s been standard that 5-7 mph over is ok. If GMP standards or other procedures are not being followed the first place to look is leadership. What is being allowed, are there procedures that contradict each other, or that have no consequences but are still expected to be enforced? #lawabiding #standards

GMPs are not merely a requirement; they are a FUNDAMENTAL VALUE for organizations manufacturing products for human consumption. These standards are essential across industries producing and commercializing goods for living beings, including raw materials, food, and pharmaceuticals. The key benefits include: 1️⃣ Consumer Safety: Ensuring products are consistently high-quality, free from contamination, and safe for human or animal use. 2️⃣ Regulatory Compliance: Meeting global standards to maintain market access and protect the company’s reputation. 3️⃣ Operational Excellence: Streamlining processes, reducing waste, and enhancing efficiency while fostering a culture of accountability and continuous improvement. How do the GMPs contribute to cost efficiency, risk mitigation, and long-term profitability? comments?

START the NEW YEAR by Ensuring Excellence with Good Manufacturing Practices (GMP)🔧 In manufacturing, quality isn’t just a goal - it’s a responsibility. Good Manufacturing Practices (GMP) serve as the cornerstone of consistent, safe, and high-quality production across industries, from pharmaceuticals to food and beyond. 🍽️💊 At their core, GMP is about fostering a culture of operational discipline, ensuring every process is well-documented, controlled, and aligned with regulatory standards. But it goes beyond compliance; GMP drives continuous improvement and customer trust 🤝. Here are three key aspects of GMP that I believe are pivotal for success: 1️⃣ 📚 Documentation is Key: If it isn’t documented, it didn’t happen. Proper record-keeping ensures traceability and accountability, critical for identifying and resolving issues quickly. 2️⃣ 👩🏭👨🏭Employee Training and Engagement: People are at the heart of manufacturing. Providing thorough training ensures everyone understands their role in maintaining quality, while fostering engagement creates a culture of ownership and pride in the work. 3️⃣ 🚀 Embracing Continuous Improvement: GMP is not a “set it and forget it” standard. Regular audits, feedback loops, and a commitment to improvement keep processes lean, efficient, and adaptable to change. At LEAN 6 QMS Consulting Services, we’ve helped organizations implement robust systems that not only meet GMP requirements but also enhance overall efficiency and scalability. 💡 How do you see GMP shaping the future of manufacturing in your field? I’d love to hear your thoughts! 🗣️ #GoodManufacturingPractices #LeanManufacturing #QualityManagement #ContinuousImprovement #ISO