GMP is to ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production.
MIVADO GP offers all the necessary support for complete conformity for your facilities, processes, and products concerning the regulations.
GMP requirements
Enabler for Quality Systems and Quality Management. Regulatory Agencies (WHO, FDA, Health Canada, EU GMP, TGA, etc…) ensure the quality of drug products by carefully monitoring drug manufacturers’ compliance with its Current Good Manufacturing Practice (CGMP) regulations. The GMP regulations for drugs contain minimum requirements for the methods, facilities, and controls used in manufacturing, processing, and packing of a drug product.
Mivado GlobalPerformance provides support and assistance in all GMP areas including Quality system implementation.
Some Areas covered in GMP
- Premises
- Equipment
- Personnel
- Sanitation
- Raw Material Testing
- Manufacturing Control
- Quality Control
- Packaging Material Testing
- Finished Product Testing
- Records
