[vc_row full_width=”stretch_row_content_no_spaces” equal_height=”yes” content_placement=”middle” css=”.vc_custom_1551448839631{background-color: #eaedf2 !important;}”][vc_column width=”1\/2″ css=”.vc_custom_1557840093074{background-image: url(https:\/\/fedegari.com\/wp-content\/uploads\/2019\/05\/Agalloco-training-FDA.jpg?id=2917) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” offset=”vc_hidden-xs”][\/vc_column][vc_column width=”1\/2″][vc_row_inner css=”.vc_custom_1551447616941{padding-right: 30px !important;padding-left: 30px !important;}”][vc_column_inner width=”1\/6″][\/vc_column_inner][vc_column_inner width=”2\/3″][vc_empty_space height=”60px”][vc_column_text]<\/p>\n
HOME<\/a> <\/i><\/b><\/span><\/span>\u00a0 NEWS<\/span><\/a><\/b><\/span><\/p>\n [\/vc_column_text][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\n [\/vc_column_text][vc_empty_space height=”45px”][vc_column_text css_animation=”fadeIn”]SEPTEMBER 23-27, 2019 – PRINCETON, NJ – USA<\/strong><\/p>\n Fedegari Group cooperates with Jim Agalloco<\/a> since years. This collaboration helped us in sharing experiences and knowledge with operators and players of phram industry not only in the US but worldwide.<\/p>\n For this reason, Fedegari is glad to introduce you the fall session of Agalloco & Associates training offerings.<\/p>\n The fall session is composed of two different courses::<\/p>\n People can take either course, but Fedegari suggests to attend both.<\/p>\n Who should attend?<\/strong><\/p>\n These courses are intended for individuals working with sterilization, aseptic processing or process validation. Experienced individuals will refine their knowledge through interaction with industry experts. Those without a strong background will learn the basics and develop an understanding of the more advanced considerations. The courses are appropriate for personnel working in QA\/QC, regulatory affairs, R&D, production, engineering, process development, validation and microbiology.[\/vc_column_text][vc_empty_space height=”15px”][vc_btn title=”FULL PROGRAM & REGISTRATION” style=”outline” shape=”square” color=”black” link=”url:https%3A%2F%2Ffedegari.com%2Fwp-content%2Fuploads%2F2019%2F05%2F2019-NJ-CourseTemplate.pdf||target:%20_blank|”][vc_empty_space height=”60px”][\/vc_column_inner][vc_column_inner width=”1\/6″][\/vc_column_inner][\/vc_row_inner][vc_empty_space height=”20px”][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” css=”.vc_custom_1551448777969{margin-top: 60px !important;margin-bottom: 60px !important;}”][vc_column width=”1\/2″][vc_column_text]<\/p>\n [\/vc_column_text][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\n September 23-25, 2019<\/strong><\/p>\n The sterilization course covers the entire range of sterilization process utilized in the pharmaceutical, biotechnology and medical device industry. Sterilization methods, validation practices and related subjects to be covered include: prerequisites for sterilization, microbiology of sterilization, use of BIs, steam sterilization for porous loads, terminal sterilization using steam, steam sterilization-in-place, dry heat sterilization and depyrogenation; gas, liquid and vapor sterilization (including isolator decontamination); radiation sterilization; filtration sterilization for liquids; compendial and regulatory considerations.[\/vc_column_text][vc_empty_space height=”15px”][vc_separator color=”black”][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\n September 26-27, 2019<\/strong><\/p>\n The aseptic course will provide comprehensive coverage of aseptic processing reviewing [\/vc_column_text][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\n Chauncey Conference Center<\/strong><\/p>\n 660 Rosedale Road, Princeton, NJ 08541<\/strong><\/p>\n Room reservation should be made directly with the hotel at 609-921-3600 or online at acc-chaunceyconferencecenter.com<\/a>[\/vc_column_text][vc_gmaps link=”#E-8_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”][vc_empty_space height=”15px”][\/vc_column][vc_column width=”1\/2″][vc_column_text]<\/p>\n [\/vc_column_text][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\n Jim is President of Agalloco&Associates<\/a>, which provides a range of technical services to the pharmaceutical and biotechnology industry. Since the formation of Agalloco&Associates in 1991, Jim has assisted more than 200 pharmaceutical, biotechnology, medical device, equipment manufacturers and bulk pharmaceutical firms in a range of validation, sterilization, aseptic processing and compliance areas. Jim has more than 45 years of industrial experience. He was previously employed at Bristol-Myers Squibb<\/a>, Pfizer<\/a> and Merck<\/a>. He has a BE and MS in Chemical Engineering and an MBA in Pharmaceutical Studies. Russell<\/a> is President of The Williamsburg Group<\/a>, engaged in pharmaceutical consulting in the areas of CGMP compliance and auditing, quality systems, design review, aseptic processing and sterilization technology, sterile filtration, due diligence evaluation, process validation, and regulatory liaison. Russel has over 45 years of experience in the pharmaceutical and related industries, including pharmaceutical manufacturing and quality control, medical devices, nutritional products, and consumer products. He has a B.S. and M.S. in Chemistry.<\/p>\n Prior to establishing TWG, Russ was employed by PDA<\/a>, Bristol-Myers Squibb<\/a>, Sterling Drug and Winthrop Laboratories. He is Vice-Chairman of ASTM Committee E55, a member of the USP Microbiology Expert Committee, Chairman of the USP Visual Inspection of Parenterals Expert Panel, a member of Pharmaceutical Technology\u2019s Editorial Advisory Board, and an Honorary Member of PDA. He has published more than fifty scientific papers, books and book chapters and is co-editor of \u201cContamination Control in Healthcare Product Manufacturing.\u201d[\/vc_column_text][\/vc_column][vc_column][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=”30px”][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” css=”.vc_custom_1551450117939{background-color: #eaedf2 !important;}”][vc_column][vc_row_inner css=”.vc_custom_1552902064695{background-color: #c4161c !important;}”][vc_column_inner][vc_empty_space height=”20px”][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":" Fedegari is glad to introduce you the fall session…<\/p>\n","protected":false},"author":7,"featured_media":2917,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[153],"tags":[154],"class_list":["post-2912","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news-en","tag-news-en"],"yoast_head":"\nAGALLOCO & ASSOCIATES 2019 TRAINING OFFERINGS<\/b><\/h1>\n
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Course Description<\/strong><\/h3>\n
Sterilization: Principles & Validation<\/strong><\/h4>\n
Aseptic Processing: Compliance & Technology<\/strong><\/h4>\n
\nbasic principles, technology choices, process design, environmental monitoring, and
\nprocess simulation. The course will includes sessions on aseptic processing risk
\nassessment, contemporary regulatory expectations and future technologies process. The
\ncourse materials and recommendations are wholly compatible with the regulatory
\nexpectations of FDA\u2019s 2004 Guideline on sterile drug products produced by aseptic
\nprocessing and EMA\u2019s \u2013 Annex 1 on Sterile Medicinal Products.[\/vc_column_text][vc_empty_space][vc_btn title=”FULL PROGRAM & REGISTRATION” style=”outline” shape=”square” color=”black” link=”url:https%3A%2F%2Ffedegari.com%2Fwp-content%2Fuploads%2F2019%2F05%2F2019-NJ-CourseTemplate.pdf||target:%20_blank|”][vc_empty_space][vc_separator color=”black”][vc_empty_space][vc_column_text]<\/p>\nCourse Location<\/strong><\/h3>\n
Princeton, NJ<\/strong><\/h4>\n
Your Instructors<\/strong><\/h3>\n
James Agalloco<\/strong><\/h4>\n
\nJim is a past President of the Parenteral Drug Association and served as an Officer or Director from 1982 to 1993. He is a current member of USP\u2019s Microbiology Expert Committee. He serves on the Editorial Advisory Boards of Pharmaceutical Technology and Pharmaceutical Manufacturing. Jim participates on the Scientific Advisory Boards of MEDInstill<\/a> and Eniware<\/a>.
\nHe has authored or co-authored more than 40 book chapters, over 140 papers and has lectured extensively on process validation, aseptic processing, and sterilization. He is coeditor of \u201cValidation of Pharmaceutical Processes\u201d, 3rd edition and \u201cAdvanced Aseptic
\nProcessing Technology.\u201d[\/vc_column_text][vc_empty_space height=”15px”][vc_separator color=”black”][vc_empty_space height=”15px”][vc_column_text css_animation=”fadeIn”]<\/p>\nRussell Madsen<\/strong><\/h4>\n