GMP Pharmaceutical

GMP - Pharmaceutical 

 

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.

GMP Certification confirms the products identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given.

Benefits of GMP Certification

  • Enhances the food safety management system
  • Increases consumer confidence in your products
  • Helps to decrease operating costs due to rework and penalties due to non-compliance
  • Helps boost export opportunities.
  • Reduced duplication of inspections
  • Cost saving

 

 

Consultancy Services Road Map:

 

  • Gap Analyses
  • Designing, Documentation and Implementation (System Development)
  • Internal Auditing
  • Management Review
  • Certification Process Guidance