Laboratory Business PartnerQuality · Validation · Compliance Contact

Independent · Netherlands & Belgium

Validation and data integrity for your lab systems — substantiated and kept current.

Periodic reviews, audit-trail sampling and change-impact assessments — performed and documented by LBP, submitted to your QA for approval.

Three principles

Traceable

Every review and sample is recorded so it can be traced.

Clear roles

LBP performs and documents; your QA approves and GxP release stays with you.

Practical expertise

We work risk-based according to GAMP 5 and CSA, within the framework of EU GMP, ISO/IEC 17025 and ISO 15189.

Who we serve

  • Pharmaceutical QC labs (GMP)
  • Hospital and clinical labs (ISO 15189)
  • Testing and calibration labs (ISO/IEC 17025)
  • MedTech and IVD (ISO 13485, IVDR)
  • Biotech
  • Contract labs

About Albert Bhoera

Albert founded LBP and has more than 25 years of experience in quality management. He led an ISO 17025-accredited site for 15 years. “Working smarter: eliminate waste and optimise processes.” More about Albert

Services

How we work

  1. Free intakeAn exploratory one-hour conversation.
  2. BaselineFixed price; credited if you start an improvement project within 3 months.
  3. Improvement projectAt a fixed price we work through the gaps together with you; your QA approves the solutions.
  4. Stay validatedMonthly maintenance of your validation status; each quarter your QA receives a report.
See all steps

Periodic system review checklist

Request the checklist by email; you will receive it within one working day.

Request checklist

Ready to talk?

Email us or call +31 6 40 90 78 31 — you will get a personal reply within two working days.