Quality Systems Development

Quality Systems are integral and vital to the successful operation of a pharmaceutical manufacturing site. We can assist in the evaluation, modification, and transfer of quality systems from the parent operations (if this applies), and in the development and implementation of new systems. We can facilitate the system design discussions that will be of benefit in ensuring that the direction of the work is the best possible to ensure that the business and regulatory needs are met. When a new operation is considered it is always a chance to develop the best systems based on experience and ensuring that the changing business and regulatory environment are taken in to account.


Regulatory Compliance and Quality Auditing

The Regulatory framework is constantly changing and it is important to get current information and a view on the emerging trends. GPN experts keep themselves up to date on these changes and issues through participation in seminars, notifications, etc. It is useful to have an independent view on a company’s operations on a regular basis to ensure compliance and to highlight areas for improvement.

The advantage of choosing the GPN auditing group to do this is that:

  • GPN see many more companies operations and you get can benefit from this experience

  • GPN have professional auditors with industry experience and know where to look for issues

  • GPN can assist in identification of improvement ideas

  • GPN can implement improvement ideas also

  • GPN experts have views on the industry trends

  • GPN are not constrained by internal company constraints


© Global Pharma Networks & Integrated Supply Chains Ltd. 2012