BIOLOGY_SERVICES.png

Services

Reduce the Risk of non-compliance

LMR Industrial Compliance offers a diverse portfolio of services across the regulated industries in the following areas:

• Regulatory Compliance
• Quality Plan & Quality Systems
• Quality Assurance & Quality Control
• FAT/SAT/Commissioning & Verification
• Qualification & Computer System Validation
• Process & Packaging Validation
• Cleaning Validation
• Food & Beverage Code & Safety
• Supplier Vendor Certification
• cGMP Audits and FDA Readiness Inspection
• GAP Analysis (as-is) & Remediation (to-be).

 

We can help.

Whether you need specific expertise and or are staff-limited, LMR Industrial Compliance can offer the professionals you need. Contact us, we are confident that we can support you to demonstrate compliance with innovative solutions.

Contact US ▸

 

Sustainable practices are Compliance.

icon2.png

Quality &
Regulatory

  • Quality Policies and Systems SOP’s

  • Quality Risk Management

  • Documents Control, Review & Approval

  • Supplier Certification & Inspection

  • Event Investigation and CAPA System

  • Customer Complaints Management

  • Annual & Periodic Product/ Data Reviews

  • Maintenance & Calibration Program

  • Food Hazard & Risks inspections & SOP’s

  • FDA enforcement action Remediation Plans

  • Training Program, curriculum and seminar

icon2.png

Qualification &
Validation

  • Commissioning and Validation Project Management

  • Development of execution strategies & SOP’s

  • Master Plan, Validation Plan, Qualification Plan

  • Commissioning, Qualifications (FAT, SAT, IOQ, PQ) & Validation:

    • Utilities, Facilities & Equipment

    • Laboratory Instrumentation

    • Method Validation

    • Cleaning Validation

    • Process Validation/ Product Transfer

    • Packaging Validation

icon1.png

Computer System
Validation (CSV)

CSV Master Plan & Validation Plan
• User Requirements & SPEC
• Traceability Matrix
• Commissioning & Qualification
PLC, SCADA, DeltaV, HMI, LIMS,
EMPOWER…
• Protocols & Plans Summary Reports
• 21 CFR Part 11 “Electronic Records & Electronic Signatures”
• CSV Vendor Audit Plan
• Serialization
• Data Integrity
• Laboratory Software