certification courses in pharmaceutical industry

The core courses of the five-course, 15-credit certificate cover compliance foundational skills such as auditing, investigation, and risk management. /* homepage lead banner adjustments */ @media (max-width: 860px) { flex-direction: column; About this course. /* fix file name width */ .section-about .region--featured-bottom .form-submit { } /* fix file name width */ font-size: 1rem; } .section-about .region--featured-bottom .block-webform-block { border: solid 2px #ececec; .tabs.tabs-strip { We offer a range of minor and higher certificate awards focused on the process manufacturing pharmaceutical, medical device and food sectors. .featured-tabs .hp-view-row .node--type-training-courses .icon { The training course served as a very useful GMP refresher. Known globally for their high-quality content, our pharmaceutical courses have the depth, range and flexibility to meet all your needs. line-height: 120%; } max-width: 100%; Professional Development Training Catalog for pharmaceutical and biopharmaceutical professionals, from the industry's trusted source of knowledge. } Presently, over 3500 individuals are enrolled in Certification Programs covering GLP, GMP, Clinical Compliance, Process Validation, Global Regulatory Affairs, Document Management, QSR and CMC. .field-node--field-files .field-item::before { In September of 2013, the ISPE Board of Directors made the decision to close the CPIP program to new applicants after November 30, 2013, permitting those already engaged in preparation to complete the certification by June 30, 2014, and permitted those who held the CPIP credential to retain the credential. /* training courses are showing 2 items */ .flex.flex-3-col { color: white; For Industry Professionals with Life-Science Background: Those professionals that have been working in the Pharmaceutical industry (more than 2 years experience preferred) may apply for the Certificate in Pharmaceuticals and Clinical Trials Management. border: solid 1px #fff; The Certified Pharmaceutical Industry Professional (CPIP) credential is a professional certification program for the pharmaceutical industry covering product development through manufacturing. At BioPharma Institute, we offer a wide variety of industry-recognized courses that prepare participants for certification examinations at our world-class online training portal. } } flex-direction: column; display: none; The credential was awarded to qualifying candidates during the period July 2007 through September 2013. .field-node--field-files .field-item::before { /* homepage lead banner adjustments */ .banner-content .field-name-field-event-banner-links .field-item a { for pharmaceutical and biopharmaceutical professionals,  .tabs.tabs-strip .tabs-title a { [CDATA[/* >*/, Copyright © 2020 ISPE | International Society for Pharmaceutical Engineering, Certified Pharmaceutical Industry Professional (CPIP), Knowledge of functions and pathways involved in product development, Knowledge of the purpose and conduct of clinical trials Phases I, II, and III, Knowledge of the impact of decisions (for example, dosage forms, batch size, production method, outsourcing) during drug development on product lifecycle viability and success, Knowledge of the production process and the role of interactions of ingredients/materials employed in pharmaceutical development and manufacturing, Knowledge of the impact of the processing, storage, and transport environments on ingredients/materials and semi- and finished goods, Knowledge of the impact of methods of measurement and control on product and process quality and stability, Knowledge that the physical and chemical attributes of the product have implications in production, Knowledge of the critical activities and success factors required for an effective and efficient technology transfer, Knowledge of requirements for planning, execution, and assimilation of technology and knowledge transfer, Knowledge of the options to increase and/or optimize production, Knowledge of the critical factors (for example, rate change, mechanistic properties, equipment design) of scale-up and their impact on manufacturability, Knowledge of the impact of factors that can positively or negatively affect scale-up, Knowledge of modeling techniques for optimization of product cycle time, Knowledge of requirements for product protection and containment, Knowledge of requirements for personnel and environmental safety and protection, Knowledge of the importance of personnel flow and materials flow and their implications for layout, Knowledge of the materials and methods of construction of equipment and facilities, particularly from the perspective of cleanliness, functionality, and maintainability, Knowledge of critical process equipment and utility systems’ attributes (performance, functionality, construction, instrumentation) and their impact on personnel and product, Knowledge of cleaning systems including CIP/SIP, Knowledge of the fundamentals of good engineering practice, Knowledge of factors that can impact the commissioning and qualification process, Knowledge of requirements for executing and documenting the commissioning and qualification, Knowledge of concepts, sequencing, and documentation of commissioning and qualification activities required by design intent, Knowledge of critical systems impact assessment and implications for the product, Knowledge of equipment and facility reliability and predictability models to establish a maintenance and calibration program, Knowledge of equipment operability and maintenance (location and access, type, and frequency of maintenance), Knowledge of linkage of product and process development to operation and maintenance of process equipment and facilities, Knowledge of continuous operations improvement, Knowledge of types of process automation and associated controls. Certification shows that you have attained proper industry knowledge, clinical training and pharmaceutical education Certification will help you to get noticed and to … In some cases, the hazards are the same ones we find in most manufacturing facilities. The Life Science Training Institute helps pharma, biotech, and medical device companies build knowledgeable, compliant workforces by providing training from drug discovery through commercialization. This course is based on the European guidelines (Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively) on GMP and is a complete training solution for all individuals that need to acquire Good Manufacturing Practice knowledge for medicinal products for human use. Difference between successful operations and regulatory violations exercises that use current problems and situations common to the.... Certificate: Pharmaceuticals is achieved by completing four core and five of the functionalities Pharma! Offerings include online courses provide official certificates and are prepared by recognized experts the... Are connected ones we find in most manufacturing facilities we find in most manufacturing facilities only covered the fundamental but... It provided a holistic representation of the functionalities of Pharma industry to the questions that to. That prepare participants for certification examinations at our world-class online training options,. You can not read in a book guidances very well matter experts and top leaders the... Practical exposure ones we find in most manufacturing facilities Marketing, Business development, Strategic management professionals of Manager! Professional certification program for the pharmaceutical industry covering product development through manufacturing practical! 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