have no critical/major findings post inspections/ audits The right people are employed and utilised in the controls Conduct regular internal and external audits Review and improve current documents (BMR/BPRs etc. during all production processes (reconcile, audit, queries resolved before QA review Responsible for compliance: Sign-on Completion Verification as per SOP Audit documents before QA review and final signoff/release requirements Training of pharmacists conducting internship and pharmacist manufacturing assistants Core
upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
upgrading their facility to be GMP compliant for SAHPRA audits. They would like to implement ISO standards too facility, to ensure the company will pass a SAHPRA audit. (They are licenced for certain products, but want
ISO standards Preparing batches and documents for audits You need at least one full year of pharmaceutical
ISO standards Preparing batches and documents for audits You need at least one full year of pharmaceutical
cleaning teams and the production teams Hygiene audits and inspections Emergency response planning Continuous cleaning teams and the production teams Hygiene audits and inspections Emergency response planning Continuous cleaning teams and the production teams Hygiene audits and inspections Emergency response planning Continuous
Safety: Ensure compliance and conduct safety audits.