This article summarizes some important considerations in the drug product formulation and process development of a new chemical entity and aims to serve as a guide to small biopharma companies in identifying desired qualities to look for when hiring a drug product development professional for their team. https://lnkd.in/eDVy8pMZ By Michelle Gischewski, KM Consulting-Pharma Intelligence
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Research could help drug developers improve the safety profiles of medications LINK: https://lnkd.in/eiAV2Qq5 Hashtags: #TodaysMedicalUpdate #Pharmaceutical #Medical #Research Please LIKE & REPOST
Research could help drug developers improve the safety profiles of medications
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🚀 **Excited to Share My Recent Experience!** 🚀 I recently had the opportunity to attend a two-day workshop on Drug Formulation and Development, hosted by BioSol. A huge thanks to Khalida Naveed for organizing and leading this insightful session. During the workshop, I gained invaluable hands-on experience with various critical databases: - **DrugRep**: Explored comprehensive drug reports and their applications. - **PDB (Protein Data Bank)**: Analyzed detailed 3D structures of proteins and nucleic acids. - **DrugChem**: Investigated chemical properties and synthesis methods of pharmaceutical compounds. - **PubChem**: Accessed extensive information on the biological activities of small molecules. This experience has significantly enhanced my skills and knowledge in drug development and formulation. Looking forward to applying these insights and continuing my journey in the pharmaceutical field! #DrugFormulation #DrugDevelopment #BioSol #ProfessionalDevelopment #Pharmaceuticals #HandsOnExperience
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"Highlighting the importance of method development and validation in our industry! As professionals in the pharmaceutical and biotechnology sectors, we understand the critical role that accurate and reliable testing methods play in ensuring the quality and safety of our products. Method development and validation are essential steps in this process, enabling us to: - Ensure accurate and precise results - Detect and quantify analytes with confidence - Comply with regulatory requirements - Advance research and development Let's continue to prioritize excellence in method development and validation, and let's keep pushing the boundaries of innovation in our field! #MethodDevelopment #Validation #Pharmaceuticals #Biotechnology #QualityMatters #Innovation"
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𝗣𝗠𝗖 𝗜𝘀𝗼𝗰𝗵𝗲𝗺 became a new 𝗔𝗙𝗦𝗦𝗜 𝗺𝗲𝗺𝗯𝗲𝗿 𝗶𝗻 𝗙𝗲𝗯𝗿𝘂𝗮𝗿𝘆 𝟮𝟬𝟮𝟰. AFSSI Sciences de la Vie is an Association dédicated to federating French service and technological innovation companies in the strategic field of Life Sciences. PMC Isochem manufactures products for the pharmaceutical and cosmetics industries. Its R&D department has a long history of developing chemical processes and analytical methods. In recent years, this activity has expanded to include research into new drugs, new excipients, new formulation solutions and protein engineering. #excipients #pharmaceutical #formulationdevelopment
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Transformational Leader in IT & Finance Program Management | 20+ Years of Experience | Driving Strategic Change at Accenture, IBM, and KPMG | Washington, DC-Based Executive Consultant
Research could help drug developers improve the safety profiles of medications LINK: https://lnkd.in/enKgwkrG Hashtags: #TodaysMedicalUpdate #Pharmaceutical #Medical #Research Please LIKE & REPOST
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Enzymes stand at the forefront of innovation within the pharmaceutical industry, offering invaluable contributions across various stages of drug development, production, and therapeutic application. These biocatalysts possess exceptional specificity and efficiency, enabling precise chemical transformations that are often challenging to achieve through traditional chemical methods. In pharmaceutical synthesis, enzymes play a pivotal role in the creation of complex molecules, enhancing both the yield and purity of pharmaceutical compounds while minimizing environmental impact. Their ability to catalyze reactions under mild conditions makes enzymatic processes not only effective but also sustainable, aligning with the industry's growing emphasis on green chemistry practices. Beyond synthesis, enzymes are integral to drug metabolism studies, aiding in the understanding of how drugs are processed within the body and informing strategies for optimizing drug efficacy and safety. This introductory role of enzymes underscores their fundamental importance in shaping the future of pharmaceutical research and development.
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🔬 Unifying Diverse Experimental Data: The Key to Enhanced Drug Development 💊 In the fast-paced pharmaceutical research world, comprehensive insights at every stage are crucial. 🌟 Data unification, especially in chemical research, plays a pivotal role in boosting drug development efficiency by seamlessly integrating diverse experimental data formats. 📊🔗 However, this is not without its challenges. Integrating varied data formats and ensuring data integrity under different conditions can be complex. 🧩🧬 But overcoming these hurdles can lead to groundbreaking advancements and more efficient drug discovery and development processes. 🚀✨ At Mangabey, we're at the forefront of tackling these challenges head-on, providing the expertise and solutions needed to unify and streamline experimental data. Together, we're paving the way for a more innovative and efficient future in pharma. 💡🔍 #Pharma #DataUnification #DrugDevelopment #ChemicalResearch #Innovation #DataIntegrity
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I am excited to share that our book, "Introduction to Quality by Design (QbD): From Theory to Practice," has just been published online, This book offers a comprehensive exploration of the Quality by Design (QbD) methodology, guiding readers from theory to practical application with accessible examples. It equips readers with both foundational and advanced knowledge, emphasizing the critical parameters necessary for designing pharmaceutical products that meet the highest quality standards. I would like to extend my special thanks to our editors, Dr. N. K. Jain and Dr. Neha Bajwa, as well as my colleagues, Ahmet Doğan Ergin Ayca Altay Benetti, PhD, Camillo Benetti , and Burcu Mesut. #Springer #QualitybyDesign #DesignofExperiment #QbD #DoE #PharmaceuticalTechnology #Pharmaceuticals Here is a link to access the book:
Introduction to Quality by Design (QbD)
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Validation of Analytical Procedures Q2 (R2)2023 #analyticalchemistry #analyticalinstruments #analysis #methoddevelopment #bioanalysis #bioanalytical #methods #pharmaceutical #laboratories #regulatorycompliance #regulatoryupdate #regulatoryaffairs #regulatorychallenges #analyticalscience #impurities #referencematerials #referencestandars #labelling #science
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Biotech and Bioinformatics Scientist |Cancer Biology, Aptamer & Virology| Helping Research Community| Founder
QSAR (Quantitative Structure-Activity Relationship)| QSAR for Drug Designing #bioinformatics #chemistry #pharmacy #pharma #pharmaceutical #bioit #biotech #biology #chemistry #biochemistry
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