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DTSTART;TZID=Asia/Kolkata:20211025T130000
DTEND;TZID=Asia/Kolkata:20211029T170000
DTSTAMP:20211013T061300
UID:MEC-bf499a12e998d178afd964adf64a60cb@biiworld.com
CREATED:20211013
LAST-MODIFIED:20211013
PRIORITY:5
TRANSP:OPAQUE
SUMMARY:Chemistry, Manufacturing & Controls (CMC): Connecting the solid oral dosage forms.
DESCRIPTION:\nReal Time Online Delivery – Live Training Sessions\nVirtual Attendance for 5 Days Training \nGuided Learning Hours – 20 (4 Hrs x 5 Days)\nComprehensive Learning Kit \n\nCourse Overview\nThis 5 Day Online Course is designed for those involved in developing new or generic solid oral drug products as formulation, analytical, process, quality or regulatory professionals. It aims to show participants how to handle risk during product development and to acquire an understanding of the product and its manufacturing process.\nThe Daily Sessions of this course covers each aspect of the development of a solid oral dosage form, including designing the product, formulation/process development, registration batch manufacture and stability set-down.\nHighlight of the Modules: Active Pharmaceutical Ingredients, Excipients, Tableting, Capsules, Container Closure Systems and Stability Evaluations. It will be backed by real situations, interactive approach, group exercises and multiple case studies.\nTrainer’s Profile\nOur expert trainer has experience of 30+years in the pharmaceutical industry and a Fellow of the Royal Society of Chemistry (RSC) with over thirty years’ experience as an analytical chemist.\nAn expert in sampling and sample preparation, chromatography (liquid and gas), spectroscopy (atomic and molecular) and pharmaceutical dissolution testing. Ex Honorary Treasurer of the RSC’s Analytical Division and led a working group on continuing professional development until July 2016.\nA PhD in analytical chemistry, worked at a senior level in a number of industrial laboratories with responsibility for the development of analytical methods capable of quantifying very low levels of organic compounds in a wide range of different sample types. These included pharmaceutical raw materials, drinking water, industrial effluent and marine biota.\nOne of the respected specialists, helping operating companies to achieve changes and extend best practices & learning by conducting numerous global training courses.\nKey Takeaways\n\nLearn and explore the Solid Oral Dosage Forms from tablets & capsules to factors affecting solubility and permeability\nDevelop strategy for Excipients, Tableting, Capsules\nUnderstand the Container-Closure Systems and Stability Evaluation\nIdentify risks associated with API properties and Active Pharmaceutical Ingredients in link with polymorphism and salt form, chirality, particle size, impurity profile, stability, toxicity and mutagenic impurities\nUpgrade your skill with several workshops: drug-excipient interactions, interpreting tableting process development data, setting dissolution specifications and trending stability data\n\nWho Should Attend\nProfessional in CMC working in:\n\nDevelopment\nRegistration\nPost Approval Lifecycle\nRisk Analysis\nNew or Generic solid oral drug products\n\nFormulation\nAnalytical Representatives\nProcess Development\nQuality Assurance Specialists\nQuality Control\nDrug Development\n\n\nCMO’s\nAnalytical and stability laboratory managers (R&D through GMP)\n\n\nFor participation details contact\nSamuel Isaac\nsamuel.isaac@biiworld.com ( mailto:samuel.isaac@biiworld.com )\n+1 786 633 1223(Canada)\nFill the details below to request your Brochure\n\n \n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n×\n
URL:https://biiworld.com/trainings/chemistry-manufacturing-controls-cmc-connecting-the-solid-oral-dosage-forms/
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