Documentation is fundamental to adequately demonstrating that GMP and GCP compliance was employed during product development and commercialization. Documentation needs to meet certain requirements to ensure data validity, product quality and product safety. If these records are poorly prepared or completed, then the clinical data obtained may not be adequately verified or relied upon by the regulatory agency to issue and approval and the manufacture or quality of a product can be negatively impacted. Therefore, it is imperative that Good Documentation Practices be followed throughout the process to ensure that regulatory requirements are met. The standard of documentation within a company can directly impact the level of success in achieving approval of drugs and manufacturing quality products that are safe.
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Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment
Recorded video session
Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility. She has helped to lead many Regulatory Health Inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who are faced with warning letters, consent decrees and those wishing to improve compliance establish more robust quality systems so that the company can succeed.