cGARD Functionality

File/Print

  • Current article, as word, plain text or PDF
  • Print all items checked, to focus on printing, as word, plain text or PDF
  • Print all items checked as an assessment, to provide template for assessment, as word, plain text or PDF

Regulations

  • Display regulations per country, and drill down to specific regulatory records

Topics

  • Provides 26 categorised searches to speed up focussed searches

Search

  • Enables searching of Regulations, Documents and GMP Manual
  • Enables searching of FDA Drugs database and warning letters database
  • Enables searching of the USA National Institute of Health Clinical Trial Government website

Tools

  • Details Pharmaceutical and Life Science Glossary
  • Contacts
  • Global Regulatory Website
  • Change Matrix, provide visibility to regulatory change history

Help/History

Details the date the database started and the history of additions to the database.

Documents

This section contains loaded, un-categorised documents, such as draft regulations, that are not yet in force, regulations and guidelines, that have been loaded as a PDF and not yet categorised, and any other documents such as Validation document templates.

GMP Manual

This is a partner Manual containing over Good Manufacturing Practice & Implementation. This GMP knowledge base is used in more than 65 countries by 10.000 professionals around the world. It has been written and is maintained and updated by GMP experts around the world. It is indispensable for pharmaceutical manufacturers, suppliers, consultants, engineering companies that need the current information readily available.



     
     

Customer References

  • I can certainly recommend Compliance Control as experts in this field and they will add value and deliver on your project. CFO, Major Pharma Company
  • Compliance Controls Consultants brought immediate expertise to our team as part of our drive into the European market. Vice President, Research & Development, Pharma Company
  • We wanted an organization with proven experience ensuring our organization can meet EU regulatory requirements. Business Development Manager, Phama Company
  • I would like to personally express my great appreciation for all your excellent work and great support with the validation of our IT infrastructure and software. Managing Director, Compounding Centre, UK
  • ComplianceControl Centre was selected because it is easy to use, quick to set up, and was a validated, cost effective solution for an organization of our size. We wanted a system that we could rapidly implement. Vice President, Research & Development, Pharma Company
  • Working with Compliance Control Consultants and their software products ComplianceControl Centre and cGARD helped us to understand the regulatory requirements of IT and business systems more clearly. IT Director, Pharma company
  • Using ComplianceControl Centre will help us to ensure that we are always inspection ready, by tracking our critical Quality and Compliance activities. Vice President, Research & Development, Pharma Company
  • It has been a pleasure working with you and your team and I am looking forward to co-operating with your company on similar projects in the future. Managing Director Compounding Centre UK
  • Based on your achievements and delivered results, we have started the process of building up our internal team for continuation of the work started by you. Managing Director, Pharma Company
  • cGARD has become the new rage here ! Sr. Manager, Documentation and Training, Major Pharma Company

 

 

    

 




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