World Compliance Seminars

Training on current Good Manufacturing practices is necessary to ensure that companies maintain their obligations to producing pure and safe drugs and medical devices. This training is intended to ensure that companies are aware of their obligations working in a field regulated by this guidelines training on current Good Manufacturing practices is necessary to ensure that companies maintain their obligations to producing pure and safe drugs and medical devices. This training is intended to ensure that companies are aware of their obligations working in a field regulated by these guidelines Why Should You Attend Current Good Manufacturing Practices (cGMP) are a series of guidelines that are intended to regulate the production of drugs and medical devices to ensure that they are produced in a safe manner. During this training, you will get an understanding of why they were developed, and how they shape the everyday procedures that oversee any given company’s work in this field. The or...

Documentation is a critical tool for ensuring GxP/GMP compliance and GMP Training In the regulated environment which must be GxP/GMP compliant, document control is the cornerstone of the quality system. It is so important that if an external audit identifies deficiencies in the document control system, the entire organization can be shut down. There are also GMP requirements for information technology. For a drug to be produced in a GxP/GMP compliant manner, some specific information technology practices must be followed. Computer systems involved in the development, manufacture, and sale of regulated product must meet certain requirements. Change control within quality management systems (QMS) and information technology (IT) systems is a formal process used to ensure that changes to a product or system are introduced in a controlled and coordinated manner. In the regulated industries, manufactures are required to use a change control procedure. In this webinar, the connection between ...