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Built for Continuity.

Five Pillars of Continuity.

QP Pro Services delivers end-to-end pharmaceutical quality expertise — from batch release to regulatory accountability — across five interconnected disciplines.

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Pragmatic compliance. Real execution.

Service 01 QP / RP Services Icon

QP / RP Services

Certified QP/RP support for
EU GMP Annex 16, batch certification and regulatory accountability.

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Service 02 QP / RP Services Icon

Operations

Hands-on GMP operational support: qualification, validation, MS&T, CCS, and shopfloor execution.

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Service 03 QP / RP Services Icon

EU Importation

End-to-end EU importation
under our Manufacturing Importation Authorisation (MIA).

Explore EU importation support
Service 04 QP / RP Services Icon

Inspection

A structured inspection readiness approach that helps clients perform with confidence during EU GMP, US FDA, WHO, and other regulatory inspections.

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Service 05 QP / RP Services Icon

Transition

Ad interim leadership or subject matter expert to secure continuity during critical periods.

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Need a broader view?

We listen carefully, understand the operational context, and identify the underlying compliance problem before recommending the right service mix.

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When to call us

New product import EU Importation
MIA readiness needed EU Importation
Inspection announced Inspections
QP batch release needed QP / RP
Interim management Transitions
QA system review Operations
CAPA remediation Operations
Post-inspection response Inspections
// Our services

Which pharmaceutical consulting service fits your situation?

Market access, batch release, GDP oversight, remediation, and interim leadership often need to work together across the same project.

MAHs, importers, manufacturers, and biotech scale-ups often need a service mix that matches their immediate compliance risk and business objective.

For MAHs, importers, and market-entry teams

Choose this route when you need EU importation governance, QP certification support, or a practical path to compliant market entry under MIA, GDP, and GMP expectations.

Explore EU importation | Explore QP / RP support | Plan a consultation

For manufacturers and quality leaders

This combination is the strongest fit when your site needs inspection readiness, operational remediation, contamination control, or hands-on support to improve GMP performance.

Explore operations support | Explore inspection readiness | Read a technical article

For transitions, growth phases, and temporary gaps

A strong fit when you need interim quality leadership, senior decision support, or continuity in a regulated operation during a period of change.

Explore transition support | Meet Walid El Azab | Meet Philippe Bollen

Support areas frequently requested by clients

Clients often ask us to support external QP oversight, batch certification, RP GDP oversight, EU importation under MIA, inspection readiness, GMP remediation, interim QA leadership, and regulated manufacturing or distribution activities.

4.9

Trusted by life-science professionals and manufacturers

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// Our testimonials

What our customers say

4.9

Achieving success through over 90% customer satisfaction

"The founders of QP Pro Services have been trusted partners for several years. Their senior QP expertise, pragmatic mindset, and deep understanding of EU GMP expectations consistently bring clarity and confidence to complex situations."

tes
A long-term manufacturing partner
Director of Quality Operations, EU Pharmaceutical Site

"What truly sets QP Pro Services apart is their inspection readiness approach. They don’t just prepare documents. They prepare people, decisions, and systems. Their support was instrumental to our successful regulatory inspection."

tes
Regulatory Lead
Global Life Sciences Company

"QP Pro Services delivers tailored solutions, not generic consulting. Their ability to combine strategic thinking with hands-on operational support makes them a key contributor to business continuity in highly regulated environments."

tes
A senior industry partner
A senior industry partner