Tumont can assist with:

• The production of all validation lifecycle documents, including plans, URS & design qualification reports; installation & operational protocols & reports; validation summary reports. We can provide complete document sets or “in-fills”.
• Authoring administrative & compliance related policies, SOPs & procedural controls.
• The review of suppliers’ documents for cGMP compliance.
• Gap analysis & remediation.
• Inventories
• In-house training of staff new to the GMP environment.