GOOD
MANUFACTURING
PRACTICES
PRESENTED BY ALAKORO RIDWAN BOLAJI
MATRIC NO:2110041088
Meaning And Intro To GMP
These are sets of guidelines and procedures that ensure the quality,
safety and consistency of pharmaceutical products during their
manufacturing, packaging and storage. It is shortly known as GMP.
The main objectives of GMP are to prevent contamination, mix-ups
and errors and to ensure that products are manufactured to meet the
required quality standards.
Examples are
• Regular cleaning and maintenance of equipments , machines ,and
facilities.
• Incoming raw materials are inspected for quality assurance.
COMPONENTS OF GMP
1. Primary Products :are the raw materials used to create a product.
2. Premises: Laboratory are the backbone of a pharmaceutical
company , and must be properly maintained and cleaned
3. People : these are the main agents of any business , so they must be
learned and experienced.
4. Procedures :All procedures taken during production must be safe
and standard.
5. Processes:
Principles Of GMP
• Create standard operating procedures (SOP)
• Enforce SOPs and work instructions
• Validate the effectiveness of SOPs
• Develop job competence of work
• Maintain system facilities and equipments.
Importance Of GMP
• To minimize risks involved in pharmaceutical products manufacturing
processes.
• It helps to reduce contamination of products.
• To ensure consistency in quality of products.
• It helps to avoid recalling of products.
• To maximize the benefits of technology.
GOOD LABORATORY PRACTICES (GLP)
PRESENTED By :ASOGBA SAMUEL.S
MATRIC NO:2110041031
These are sets of principles to assure the quality and integrity of non-
clinical laboratory studies.
RISKS ASSESSMENT
PRESENTED BY: AGOSU AYOMIDE SETON
MATRIC NO:2110041096
A risk assessment is the process of identifying what hazards exist, or
may appear in the workplace, how they may cause harm and to take
steps to minimise harm
IMPORTANCE OF RISKS ASSESSMENT
• To identify health and safety hazards and evaluate the risks presented
within the workplace
• To evaluate the effectiveness and suitability of existing control
measure
• To ensure additional controls (including procedural) are implemented
wherever the remaining risk is considered to be anything other than
low.
• To create awareness among employees and use as a training tool
• Save costs by being proactive instead of reactive
Risk assessment control measures
• Elimination control
• Substitution control
• Engineering control
• Administrative control
• Personal protection control