Best Pharmaceuticals QMS Services In India

·       Redesigning of SOP and other documents of Plant.

·       Qualification and Validation: Qualification and Validation are integral steps in building quality into any facility. ARS provides an efficient and effective documentation system that meets the requirements of International Regulatory authorities.

  • Validation Protocol Preparation & Execution.
  • Validation Master Plan.
  • Deign Protocols.
  • IQ protocols for all types of Equipment.
  • OQ Protocols.
  • PQ protocols.
  • Conducting Process Validation at your site.
  • Area Validation. (HVAC)
  • Purified Water Validation Protocol & Validation.

·       Manual Preparation.

  • Site Master File.
  • Validation Master Plan.
  • Quality Manual.
  • Safety Manual.
  • Training Manual.

·    Standard Operating Procedures (All department present in unit).

  • Quality Assurance Procedures.
  • Quality Control Procedures.
  • Warehouse/Store.
  • Engineering / Maintenance.
  • Production.
  • Human Resource.

·    Redesigning of Manufacturing batch records and Batch packing Record.

·    Redesigning of Specification and Method of analysis.

·    Redesigning of Master Formula Record.

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