Please download one of these browsers:
Keep your browser version up-to-date for a fast, secure, web experience.
This course will provide you with an overview of what matters in validation of computerised systems (including CSA) to help your company meet regulatory requirements and mitigate risks to product quality and patient safety.
This course introduces Supplier QA concepts and practices within a Quality Management Systems (QMS) so you understand why Supplier QA is important, and how suppliers are classified and controlled based on risk.
This course provides an introduction to Quality, Quality Management Systems, International Standards Organisation (ISO), ISO 9001, ISO 13485 and CAPA.
This course provides a solid introduction to Good Manufacturing Practice (GMP) for pharmaceutical products through control and management of manufacturing and quality.
This course provides an overview of how GMP applies to the warehouse with respect to receipt, storage, issue and distribution.
This course addresses the importance of implementing and complying with cleaning and sanitising procedures and why the responsibilities apply to all GMP staff (not just cleaners).
This course looks at the role of GMP documentation in providing a history of manufacturing from supplier to customer, including the requirements of master instructions, Standard Operating Procedures (SOPs), batch records, quality control records and how to complete GMP records.
This course provides an introduction to the types, sources, risks and control measures of contamination in relation the manufacturing of pharmaceutical products.
This course looks at the controls for starting materials, dispensing and processing, then it addresses what actions to take when confronted with a deviation and how to calculate yield and reconciliation.
.png?lmsauth=6e99c488c4293c9c01f31dc24f514d67339eb26d)
