Pharmaceutical's Documentation
“In Pharmaceuticals industries its documentation is like a Nerve System & Quality Assurance department is like a Brain which control and runs it throughout the organization. Documentations impacts your quality, organization growth, regulatory compliance, Piracy & Healthy environment”
Project Documentation
Project charters/Report, design documents, tendor Documentaion, Technology Transfer Documentation Etc.
Equipments Validation
Machine, URS, (TBA)Technical Analysis Document, CBA, PO, DQ, FAT, SAT, IQ, OQ, PQ Etc.
Area Validation
Clean Rooms validation, HVAC Validation, Viable & Non-Viable Particle/Microorganism Monitoring & Controls.
Process Validations
Process Validation Batches Protocols, Reports & Trend generation . Cleaning Validation Protocol, reports & trend analysis.
Quality Method Validation
Analytical Methode validation (AMV), Validation of Microbiological Methods
Policies & Other Documentation
HR Policies, Vendor management Policies, Quality Policies, Safety Policies, Data Integrity policies, Etc.
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Pharmaceutical Process Awareness
Pharma Plants Process awareness, Best Equipment in the Markets, Product awareness, Different Compliance awareness, All world Market Regulation Awareness & Awareness about Many technical aspects.