GxP Consultancy

GxP Consultancy
Product Description

With over 5,000 projects delivered across pharmaceutical, biotech, and medical device organisations, our consultants bring the depth of experience that only comes from years embedded in the realities of GxP-regulated manufacturing and supply chains. We don't hand you a report and walk away. We work alongside your teams, assessing, planning, building, and validating, so that when the regulator arrives, you're not just ready, you're confident. Whether you're remediating a critical finding, preparing a site for inspection, or building a validation strategy from the ground up, we bring the technical authority and hands-on partnership to get it right. • Compliance Readiness Assessments & Gap Analysis • Remediation Planning & Implementation • Supplier & Internal Audits • Preparation for Regulatory Inspections • Validation Master Plans, Process & Cleaning Validation • Equipment Qualification • Training Services

Rephine Barcelona SLU

  • Country/Region:
    Spain
  • On CPHI since:
    2023
  • Employees:
    100 - 249
Company types
Consultancy

Rephine Barcelona SLU

  • Country/Region:
    Spain
  • On CPHI since:
    2023
  • Employees:
    100 - 249
Company types
Consultancy

More Products from Rephine Barcelona SLU (4)

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  • Training Services

    Product Training Services

    Integrated services. One quality partner. We combine specialised consultancy, digital innovation and world-class audit capabilities to help you solve your most complex quality challenges. GxP Consultancy With over 5,000 projects delivered across pharmaceutical, biotech, and medical device organisations, ...
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    Backed by over 10,000 audits across 1,200+ sites worldwide, our audit services set the benchmark that health authorities and client’s alike trust. From our industry-leading shared audit library to fully bespoke engagements, every report is built on a methodology that has been independently validated and re...
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    Product Regulatory

    Bringing a medical device to market, and keeping it there, demands precision at every stage, from classification and risk assessment through to post-market surveillance. Our specialists guide you through the regulatory and quality requirements of the device lifecycle, whether you're navigating MDR, buildin...