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Arivis offers solid solutions for contract manufacturing. Pharmaceutical manufacturers contract out any quality control testing, will need a licensed laboratory, certified as a GMP or GLP. With a biomedion you are committed to integrity with contract testing laboratories. Microscopes have enabled researchers to conduct in-depth academic and exploratory research.

The biomedical research and engineering sector is driving innovation by microscopy techniques to produce better and more informative images of cellular functions, including internal images of cells. Achieve process adherence by post-implementation training. Organizing logistics and resources Scheduling learning Handling instructor-led training administration — Virtual or Classroom based registration confirmations, reminder emails,… Advanced Monitoring process adherence, effectiveness, user experience, forecasting systems performance,… Creating reports and business intelligence Managing upgrades and post implementation ramp-on phases Creating learning resources with arivis5D Upload content Deliver courses online Onboarding process User Enrollment, Learning plans Ramp-up new users Tracking and assessing learner performance.

To summarize, here is a visual that illustrates the post-implementation training process steps with audience: The post-implementation training methodology facilitates changes effectively and increases system-related process adherence within an organization.

Related Processes. Read More. Audit Management The increasing complexity and continuous changes in the regulatory environment push organizations to seek a more holistic and highly integrated approach to their audit management processes. CAPA Management To understand how to achieve quality in a regulated industry, you need to know that corrective and preventative actions CAPA are essential elements of quality management in GxP environments. Change Control Change management is specifically designed to evaluate, redesign, and implement new business processes, where processes are defined in standard operating procedures SOPs.

High Content Screening High-content screening HCS , also known as high-content analysis HCA or cellomics , is a method that is used in early development stages and drug discovery to typically identify substances such as small molecules, peptides, or relevant RNAi that can lead into development candidates for future medicines. Image Annotation With the development of diagnostic imaging devices, large amounts of digital high-res and 3D images are generated every day. CRO Collaboration The last few years have seen tremendous consolidation in both the pharmaceutical and contract research industries.

Remote Image Analysis Imaging data in diagnostics and research is growing at an unprecedented rate, coming from all kinds of sources. Inspection Management Regulatory agencies conduct routine inspections during active studies. Training Management Post implementation training services relate often to process changes.

The TMF allows independent auditors and regulatory authorities to monitor and evaluate the quality of the data produced by a clinical study. Raw Data How to manage huge amounts of Laboratory data. Raw Data How to improve internal audit and regulatory inspection readiness. Raw Data How to improve internal audit and regulatory inspection readiness How an OS in life sciences can drastically decrease inspection preparation time Zeitverschwendung ist die leichteste aller Verschwendungen.

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