What is GMP (Good Manufacturing Practice) Certification?
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process – every time a product is made. It is a voluntary standard therefore it automatically fulfils the expectations of the customers and stakeholders regarding product quality and basic food safety practices.
What are the 4 pillars of GMP?
Good Manufacturing Practices (GMP) is a comprehensive manufacturing system that ensures product consistency and quality by addressing 5 key components: products, people, processes, procedures, and premises.
What are Benefits of GMP Certification?
- Increased customer confidence
- Control & eliminate the risks that affects final product
- Ensure sustainable quality system to reduce the errors
- Ensure safe product use for humans
- Fulfill the regulatory requirements
- Prevent mislabeling & adulteration
- Enhance your brand image
- Helpful in attracting new customers
- Helpful to retain the confidence of existing customers
- Increase the company’s revenue, profitability by reducing cost.
What are the criteria of GMP Certification?
- Quality system
- Quality training
- Document controls
- Device master record
- Non confirming product
- Corrective and preventive action
- Internal quality audit
- Management review meeting
- Risk management
- Product testing
- Process control