Quality, Compliance & Validation

Proven Quality through an independently validated QMS.

AGR Automation Ltd are committed to supplying quality Products and Services, we achieve this by employing an effective and independently validated QMS (Quality Management System)
Inclusive of procedures covering Environmental and Health & Safety systems, AGR operate 70 separate audited procedures to ensure our products and services and operations meet or exceed our client’s expectations.

Independently audited and approved by BSI twice yearly AGR continue to meet or exceed all the standard requirements of ISO9001:2008
International Regulatory Compliance

All AGR Automation Machinery and equipment is supplied fully compliant to applicable EN Directives, utilising fully trained validation and compliance engineers, all systems are designed, assessed and validated to meet all applicable EN directives required to achieve compliance to the Machinery Directive 2006/42/EC. With an internal library of over 112 current EN Directives clients can be sure the equipment they receive meets all applicable and in most cases pending releases of EN directives. Machinery is often also supplied to meet additional requirements of UL and OSHA 29CFR standards applicable in the USA and Canada.
 
Validation of Automated Equipment & Machinery (cGMP and GAMP)

AGR Automation Ltd have a proven track record in the supply of fully validated machinery and systems to meet the exacting requirements of the FDA and other approving bodies. To achieve trouble free smooth approval AGR Automation Design, Build, Commission and Validate systems by adopting cGMP and GAMP guidelines. AGR Automation has a proven record of validation having supplied equipment to many Global leading Medical Device manufacturers
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