Leveraging SeerPharma’s vast and extensive experience working in the industries to which we consult, our clients benefit from our ability to quickly understand their areas of concern and provide pragmatic and practical advice. With a thorough working knowledge of all relevant industry regulations and guidance, we help our clients implement effective and compliant business practices to improve their overall performance.

Contact us for advice and assistance with:

  • Products
    • Pharmaceuticals (all dosage forms, sterile and non-sterile)
    • Medical devices, medical software and mobile medical ‘apps’
    • Biologicals
    • Cellular, blood and tissue therapies
    • Software products (e.g. QMS, LMS, LIMS, ERP/MRP)
  • Areas
    • Good Manufacturing Practices (GMP)
    • Good Practices such as Clinical, Laboratory and Distribution/Wholesaling (GxP)
    • Facility design and licensing (including FDA and TGA)
    • Validation Master Plan (VMP) and execution
    • Quality Assurance (QA) and Quality Management Systems (QMS)
    • Internal and external audits and inspections
    • Risk assessment and risk management
    • Vendor assurance and supply chain management
    • Computer Systems Validation (CSV)
    • IT Project Management
    • Equipment qualification
    • Process validation
    • Analytical method validation
    • Contamination control
    • Product Quality Reviews (PQR)
    • Release for supply
    • Conformity assessment
    • Continuous improvement
    • Regulatory Affairs (RA)