True: The Medicines Act 1968 sets out the legal framework for the manufacture, supply, and sale of medicines in the UK., The Human Medicines Regulations 2012 updated and consolidated the requirements of the Medicines Act 1968., The General Pharmaceutical Council (GPhC) regulates pharmacy professionals and ensures pharmacies meet legal standards., MHRA (Medicines and Healthcare products Regulatory Agency) monitors the safety of medicines and medical devices in the UK., Good Manufacturing Practice (GMP) ensures that products are consistently produced to quality standards., Cleanliness, correct labelling, and controlled environments are essential parts of safe manufacturing., All equipment must be calibrated and maintained to prevent errors in manufacturing., Staff training and competency checks are part of maintaining safe manufacturing practices., Standard Operating Procedures (SOPs) provide step-by-step instructions to ensure consistent and safe practice., Any errors in manufacturing or dispensing must be recorded and investigated., Effective incident management includes reporting, investigation, corrective action, and learning to prevent recurrence., False: Following legislation is optional if a pharmacy believes its own procedures are safe., Risk assessments are not required if the product being manufactured is commonly used., Deviations from SOPs should always be ignored if they seem minor., Near misses do not need reporting because no actual harm occurred.,

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