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Pharmaceutical Validation Services

Pharmaceutical Validation Services

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Pharmaceutical validation services
Cold Storage Validation
Steam Sterilization Validation
Instrument Validation
Oven Validation
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3 Qms Serivces

Thane, Maharashtra
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Product Description

Pharmaceutical validation services
Cold Storage Validation
Steam Sterilization Validation
Instrument Validation
Oven Validation
Pharmaceutical Validation
Centrifuge Validation
Freezer Validation
Validation Protocols
Lab Equipment Validation
FDA Compliance Validation
GxP, GMP, cGMP Compliance Validation
FSMA Compliance Validation
Temperature Mapping Validation
  • Manufacturing Process Validation (PV): Bio, Vaccines, Pharma, Med Devices, Consumer Products
  • Packaging Process Validation (Pkg V)
  • Cleaning Validation (CV)
  • New Approaches to Cleaning Validation
  • Analytical Methods Validation & Transfer
  • Software Validation and CSV 21 CFR Part 11
  • Network / IT Infrastructure Validation
  • Risk Based C&Q, Cleaning and Process Validation
  • Validation Master Plans
  • Maintenance of Validated Status: Verification vs. Validation? We apply QRM most recent approaches Revalidation
Warehouse Temperature Mapping
Cold Storage Validation
Steam Sterilization Validation
Instrument Validation
Oven Validation
Pharmaceutical Validation
Centrifuge Validation
Freezer Validation
Validation Protocols
Lab Equipment Validation
FDA Compliance Validation
GxP, GMP, cGMP Compliance Validation
FSMA Compliance Validation
Temperature Mapping Validation

    Manufacturing Process Validation (PV): Bio, Vaccines, Pharma, Med Devices, Consumer Products
    Packaging Process Validation (Pkg V)
    Cleaning Validation (CV)
    New Approaches to Cleaning Validation
    Analytical Methods Validation & Transfer
    Software Validation and CSV 21 CFR Part 11
    Network / IT Infrastructure Validation
    Risk Based C&Q, Cleaning and Process Validation
    Validation Master Plans
    Maintenance of Validated Status: Verification vs. Validation? We apply QRM most recent approaches Revalidation

    Green Building Commissioning
    Manufacturing and Packaging Equipment Qualification (IQ,OQ,PQ)
    Design Qualification (DQ)
    Maintenance System Qualification
    Utilities Qualification
    Facilities Qualification
    FAT / SAT
    Risk Assessment and Risk Management: Direct vs. Non-Direct Impact; Critical Vs. Non-Critical
    Commissioning and Enhanced Commissioning
    Decommissioning
    Integrated Validation Approach
    Suppliers / Materials







We can prepare SOPs related to CSV and other verticales of the Manufacturing and research services
GAMP 3,4,5, System categories & Validation methodologyVMP - Validation Master Plan -
GAP Assessment-
URS -User requirement specification-
Initial Risk Assessment-
Vendor Assessment-
21 cfr part 11 Assessment-
Validation Plan-
FCS - Functional configuration specification-
QRM -Quality Risk Management -
Risk Acceptance & Risk Management -
IQ- Installation Qualification-
OQ -Operational Qualification-
pq -Performance Qualification-
Discrepancy reports-
TM -Tracebility Matrix-
VSR-Validation Summary report-
System Retirement-
System Revalidation /Periodic review-
Test Plans/Test Protocols-
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Pharmaceutical Validation Services

Company Details


About the Company

Legal Status of FirmPartnership
Nature of BusinessService Provider
Number of EmployeesUpto 10 People
Annual TurnoverUpto Rs. 50 Lakh
IndiaMART Member SinceSep 2019
  1. Computer System Validation Services
  2. Software Validation Services
  3. Spreadsheet validation Services
  4. Cleaning Validation services
  5. Web application Validation services
  6. Data Integrity Services
  7. ,ALCOA+
  8. Medical Devices 510k services
  9. IT-Auditing (Internal/External)Calibration medical devices

  1. GAMP5,-System categories & Validation methodology
  2. End to End Life cycle CSV implementation
  3. GAP Assessment
  4. URS -User requirement specification
  5. Initial Risk Assessment
  6. Vendor Assessment
  7. 21 cfr part 11 Assessment
  8. Validation Plan
  9. FCS - Functional configuration specification
  10. QRM -Quality Risk Management
  11. Risk Acceptance & Risk Management
  12. IQ- Installation Qualification
  13. OQ -Operational Qualification
  14. pq -Performance Qualification
  15. Discrepancy reports
  16. TM -Tracebility Matrix
  17. VSR-Validation Summary report
  18. System Retirement
  19. System Revalidation /Periodic review
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Seller Contact Details

Sahi Kumar

Kumar Buildings
Thane - 400602, Maharashtra, India

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