Just released! Part one of a new ValSource Viewpoints safety-focused podcast series. This episode, led by ValSource Inc. Director of Learning James Vesper, features Senior Safety Consultant Arthur Limper, an industry leader known for his successful career enhancing safety protocols and promoting best practices across all aspects of pharmaceutical manufacturing and operations. From 2002-2021, Limper was responsible for the development and implementation of Merck Global Engineering Solutions' award-winning Health, Safety and Environment (HSE) program for employees and contractors, which produced year-to-year, continuous drops in recordable and Days Away, Restricted, or Transferred (DART) injuries. Limper has been a key contributor to ValSource Safety Solutions, a comprehensive program combining ValSource consulting services and resources with PIMSHQ’s innovative PIMS Safety software. Listen Now: https://lnkd.in/g6TpVxP3 #SafetySolutions #RiskManagement #NationalSafetyMonth #WorkplaceSafety #SafetySoftware
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Couldn't join the "𝗛𝗼𝘄 𝘁𝗼 𝗘𝗻𝘀𝘂𝗿𝗲 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲 𝘄𝗶𝘁𝗵 𝗔𝗻𝗻𝗲𝘅 𝟭" PharmaLex webinar? No problem - we recorded it for you! 🚀 Access this #webinar and learn about these challenges, based on our experiences within the industry, and how companies can have a structured approach helping them to make the assessment. 𝗦𝗽𝗲𝗮𝗸𝗲𝗿𝘀: 🎙️Patrick Nieuwenhuizen, Director Principal Consultant at Cencora PharmaLex 🎙️Londa R., Quality Director, Quality Management & Compliance at Cencora PharmaLex 𝗞𝗲𝘆 𝗹𝗲𝗮𝗿𝗻𝗶𝗻𝗴𝘀: ➡️ QRM; ➡️ CCS; ➡️ Case study examples of aging facilities; ➡️ Annex 1 Gap assessment and remediation plans – a step-by-step approach. Register and access the webinar recording here: 🔗 https://rebrand.ly/6yo6juf #CencoraPharmalex #Annex1
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Ups, we did it again!😉 Completed the Highwire Independent Safety Assessment Programme. The results provide a strong indicator of how we value safety and are a reliable predictor of future performance. Nevertheless, the achieved result places us all in the top tier globally, within the top 18% of companies and performers in the world in this category. Bravo, Cleangrad! #safety #cleanrooms #pharma #Cleangrad #riskassessment
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Couldn't join the "𝗛𝗼𝘄 𝘁𝗼 𝗘𝗻𝘀𝘂𝗿𝗲 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲 𝘄𝗶𝘁𝗵 𝗔𝗻𝗻𝗲𝘅 𝟭" Cencora PharmaLex webinar? No problem - we recorded it for you! 🚀 Access this #webinar and learn about these challenges, based on our experiences within the industry, and how companies can have a structured approach helping them to make the assessment. 𝗦𝗽𝗲𝗮𝗸𝗲𝗿𝘀: 🎙️Patrick Nieuwenhuizen, Director Principal Consultant at Cencora PharmaLex 🎙️Londa R., Quality Director, Quality Management & Compliance at Cencora PharmaLex 𝗞𝗲𝘆 𝗹𝗲𝗮𝗿𝗻𝗶𝗻𝗴𝘀: ➡️ QRM; ➡️ CCS; ➡️Case study examples of aging facilities; ➡️ Annex 1 Gap assessment and remediation plans – a step-by-step approach. Register and access the webinar recording here: 🔗 https://bit.ly/3t850ue #CencoraPharmalex #Annex1
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We're pleased to introduce the latest installment in our Q&A with Ardena Expert series, featuring Rob Abbenhuis, CHEM Division Manager at Ardena. Join us as we delve into the fascinating world of #HighlyPotentAPIs (HPAPIs) and their safe handling in drug development. In this Q&A with Ardena Experts, we'll explore: 🟠 The significance of #HPAPIs in drug development. Occupational Exposure Banding (#OEB) and its role in worker safety. 🟠 Ardena's state-of-the-art capabilities in handling Highly Potent materials. 🟠 Innovative measures in place to ensure #SafeHandling at our manufacturing facilities. Do you want to learn more about: - The principles of segregation and pressure cascading for worker protection? - The crucial role of process development in API manufacturing? - The concept of #DesignSpace and its impact on #Quality and #Safety? Read below the full Q&A where Rob Abbenhuis provides expert insights on these topics and more! #ArdenaQandA #ExpertInsights #DrugDevelopment #CDMO #OccupationalSafety #ManufacturingExcellence #InnovativeSolutions #QualityAndSafety #ProcessDevelopment
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📢We need your help! 🗣️A representative from our Annex 1 initiative at BioPhorum will use the knowledge shared within the workstream on 'quality considerations for single-use systems used in aseptic processes' to support EU GMP inspector training. 🌍The event will be hosted by the European Commission from 17-19 April 2024. 📄Do you have a case study to share capturing the challenges and benefits of implementing single-use systems (SUS)? Let us know in the comments below 👇 #BioPhorum #SUS #SingleUseSystems #CaseStudyrequest #Annex1
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Providing Contamination Control Strategy, & Cleaning Validation Solutions to the Pharma & Biotech Industry
📢 All BioCleaning Consulting followers, we will have our event tomorrow on "Developing Comprehensive Cleaning Protocol" at 10:00 AM, AEST 😛 Secure your spot and let's have a high-level discussion with our Quality Expert, Luis Rojas LEVEL UP your Cleaning Validation approach and earn BONUSES with us 🎁 register here 👉 https://lu.ma/75cng9bj 👈 ******************************* WHY DO I WANT TO JOIN? 😅 We are aware that the devil is in the details, therefore during this webinar, we will cover every aspect of developing a rigorous cleaning protocol. In order to achieve excellence in Cleaning Validation, we want to provide you with the information and skills you need to successfully negotiate the constantly changing regulatory environment. Here you will learn: -Defining the scope and objectives of the cleaning process -Identifying the appropriate cleaning procedures -Establishing acceptance criteria for the cleaning process -Practical examples of cleaning processes in real-world settings JOIN US NOW! #webinar #online #cleaningvalidation #gmp #cleanroom #fda #rootcauseanalysis
📢 All BioCleaning Consulting followers, we will have our event tomorrow on "Developing Comprehensive Cleaning Protocol" at 10:00 AM, AEST 😛 Secure your spot and let's have a high-level discussion with our Quality Expert, Luis Rojas LEVEL UP your Cleaning Validation approach and earn BONUSES with us 🎁 register here 👉 https://lu.ma/75cng9bj 👈 ******************************* WHY DO I WANT TO JOIN? 😅 We are aware that the devil is in the details, therefore during this webinar, we will cover every aspect of developing a rigorous cleaning protocol. In order to achieve excellence in Cleaning Validation, we want to provide you with the information and skills you need to successfully negotiate the constantly changing regulatory environment. Here you will learn: -Defining the scope and objectives of the cleaning process -Identifying the appropriate cleaning procedures -Establishing acceptance criteria for the cleaning process -Practical examples of cleaning processes in real-world settings JOIN US NOW! #webinar #online #cleaningvalidation #gmp #cleanroom #fda #rootcauseanalysis
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A common question asked: Do mushrooms (or shrooms) show up on a drug test? Although the Department of Transportation (DOT) 5-panel tests for marijuana, cocaine, PCP, opioids, and amphetamines, other substances, such as mushrooms, pose a safety concern and supervisors and managers must remain aware. Employers with workers in safety-sensitive positions have responsibilities to ensure the safety of their employees and the public. Supervisors need to be prepared on how to look for signs and symptoms of impairment of any substance, and what to do next. View ASAP’s Supervisory Trainings here: https://ow.ly/VrN850QAcqQ
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All my contacts that use single-use systems (#SUS) in fill-finish, if you have any case studies that highlight the challenges and benefits of implementing SUS, especially considering the updates to #annex1 let me know.
📢We need your help! 🗣️A representative from our Annex 1 initiative at BioPhorum will use the knowledge shared within the workstream on 'quality considerations for single-use systems used in aseptic processes' to support EU GMP inspector training. 🌍The event will be hosted by the European Commission from 17-19 April 2024. 📄Do you have a case study to share capturing the challenges and benefits of implementing single-use systems (SUS)? Let us know in the comments below 👇 #BioPhorum #SUS #SingleUseSystems #CaseStudyrequest #Annex1
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The Voice of Compliance*Founder of The Compliance Podcast Network*Evangelizing for and Serving the Compliance Community
🔍 Elevate your compliance game with the latest insights from Data-Driven Compliance! In our newest episode, I sit down with James Dawson, Chief Compliance Officer at Qordata, for a deep dive into "Data-Driven Compliance in the Pharmaceutical Arena." Jim Dawson, a compliance expert, discusses the power of data in enhancing compliance programs, highlighting its role in identifying patterns, preventing risks, and promoting transparency. Tune in now to the Data-Driven Compliance podcast with me and Jim Dawson! 🎧 https://bit.ly/46VhQti #DataDrivenCompliance #PodcastAlert
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QA Webinar with case study example of aging manufacturing facility and how to put in compliance measures
Couldn't join the "𝗛𝗼𝘄 𝘁𝗼 𝗘𝗻𝘀𝘂𝗿𝗲 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲 𝘄𝗶𝘁𝗵 #𝗔𝗻𝗻𝗲𝘅𝟭" PharmaLex webinar? No problem - we recorded it for you! 🚀 Access this #webinar and learn about these challenges, based on our experiences within the industry, and how companies can have a structured approach helping them to make the assessment. 𝗦𝗽𝗲𝗮𝗸𝗲𝗿𝘀: 🎙️Patrick Nieuwenhuizen, Director Principal Consultant 🎙️Londa R., Quality Director, Quality Management & Compliance Register and access the webinar recording here: 🔗 https://lnkd.in/dBctjAia
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