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We can manage or execute on your behalf :
Process improvement projects (including WCM, Lean Manufacturing, Quality)
Process validation (planning, design reviews and protocol drafting and execution)
Pharmaceutical equipment validation
GLP/cGMP Quality Management Systems or GAP audits and assessments
Approval processes for all international regulatory authorities (FDA, MHRA, EU, TGA, WHO), including Part 11 compliance
OutSourced, professional staff available at short notice for long or short duration assignments (Engineers, Validation professionals, GMP experts
Please contact us to discuss your needs.


Extensive list of pharmaceutical software options summarised for your convenience. LIMS, CAPA, Change Control, CMMS, Sarbanes-Oxley etc software options?