SEEKPro for Pharma

SEEKPro helps pharmaceutical companies create a self-sustained culture of quality excellence, with a strong focus on Data Integrity. Backed by its parent company, Manford - with 24 years of research and experience under its belt - SEEK uses its state-of-the-art technology platform to align Processes, Systems and People, resulting in higher productivity and consistent quality excellence.

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SEEKPro Solutions

  • - SEEK provides lead indicators on compliance risk and thereby help taking proactive steps
  • - Keep the employees informed about the latest regulatory requirements and changes
  • - Help implement the latest regulatory practices
  • - Identify regulatory deficiencies
  • - Identify unintentional compliance issues
  • - Generates adaptive assessment as per employee’s role and responsibilities
  • - Skill Gap Analysis
  • - Customized content based on assessment scores
  • - Makes SOPs interactive and short
  • - Confidential platform that helps employees raise their concerns anonymously
  • - Identifies process implementation challenges
  • - Gets to the pulse of the organization by asking the right leading questions
  • - Identifies intentional compliance issues
  • - Provides insights on Employee Engagement & Attrition Risk
  • - Rewards and Recognizes top talent
  • - Highlights employee concerns

Technical Content - Snapshot

  • F & E
  • Production
  • QC
  • R & D
  • QA
  • Warehouse
  • GDP
  • GMP - Overview of 21 CFR-Part 210 & 212
  • Deviation Management
  • Management of Market Complaints
  • Process validation
  • Installation Qualification
  • Data Integrity
  • Operational Qualification
  • Personal protective equipment
  • Management of Standard Operating Procedure
  • And More
  • GDP
  • GMP- Overview of 21 CFR - Part 210 & 212
  • Control & monitoring of cross contamination
  • Management of Market Complaints
  • Change
    Management
  • Data Integrity
  • Deviation
    Management
  • Quality Risk
    Management
  • Product Quality
    Review
  • And More
  • Deviation-(planned and unplanned)
  • Change Control
  • Out of specification (OOS)
  • Calibration of instruments
  • Market recalls
  • Handling of non-conformance
  • Post release monitoring-complaints, recalls
  • Impurities (known and unknown) : ICH guideline
  • Deviations Planned and Unplanned
  • And More
  • Clinical research process
  • GMP- Overview of 21 CFR — Part 210 & 212
  • Pre-formulation and formulation development activities
  • Requirements for registration and approval
  • Technology transfer methods
  • Understanding on IND, NDA, ANDA/Dossiers
  • Analytical method development
  • Process/method/cleaning validation
  • Deviations Planned and Unplanned
  • And More
  • Pre- Audit preparation
  • cGMP compliance
  • Root cause analysis
  • Calibration, Equipment and Validation
  • Instrumentation required for QA
  • Quality Standards
  • Quality Documentation and
    Review Procedure
  • Good Manufacturing / Laboratory Practices and Audit
  • Regulatory Aspects of
    QC/QA
  • And More
  • Good Warehouse Practices
  • EHS Risk Assessment and Management
  • Adverse EHS events investigation and Reporting
  • Procedure for Stock Reconciliation (Physical Inventory)
  • Handling of Temperature sensitive drug substance & Drug products
  • And More

SEEKPro Reports

  • Compliance Risk Assessment Report
  • Skill Gap Report
  • Roadblocks to Quality Excellence
  • Employee Attitude Assessment Score
  • Employee Skill Index
  • App Usage Report
  • Attrition Risk
  • High Performing Talents

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