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© 2026 cohaga AG · All Rights Reserved · St. Gallen, Switzerland · Imprint745,110 companies indexed · Last updated: today
DirectoryBusiness & Technical ServicesManagement ConsultingRiehenPharmaKorell GmbH
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Verified· 3 sources

PharmaKorell GmbH

Summary

About the company

The core activity of PharmaKorell GmbH is the consulting and support of companies in the pharmaceutical industry, particularly in the areas of quality management (GMP, GDP, ISO 13485) and regulatory affairs. The company offers services such as audits, expert opinions, training and interim management to support companies in complying with quality standards and regulatory requirements.

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Products & services

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Quality management and GMP/GDP compliance consulting
Consulting in quality management, GMP and GDP compliance as well as ISO 13485; support for quality assurance, organisational structures and cost-effective implementation in the pharma environment.
Qualified Person (QP) / Responsible technical person (FvP) for batch release and certification
External Qualified Person in Germany and Technical Responsible Person in Switzerland; batch release and certification of medicinal products and active substances, including via own authorisations.
Audits and due-diligence assessments
Quality assurance audits, due-diligence audits and supplier qualification; on-site audits, questionnaire-based audits and evaluation of additional information for GMP, GDP, ISO 9001 and ISO 13485.
Support for regulatory inspections
Preparation for GMP regulatory inspections with pre-audit, preparation plan, staff training, accompaniment during the inspection and subsequent action planning.
Creation of GMP documents
Creation of site master files, master plans, policies, risk analyses, qualification and validation documents, SOPs, manufacturing and testing specifications, stability plans, forms and checklists.
Training sessions and workshops
In-house training sessions, public training sessions, conferences as well as presentations and workshops on GMP, risk management, validation, audits, inspections and regulatory topics.
Import into the European Union
Import of finished medicinal products and active substances into the EU, including own manufacturing authorisation, import authorisation, storage capacities and organisation of EU branches.
Development of new business areas and partnerships
Support for new business areas, regulatory authorisations, product development, extension of the value creation chain, partner search and regulatory pre-assessment.
Compatibility and stability studies
Planning, execution, evaluation and reporting of compatibility and stability studies together with GMP contract laboratories, including study design and audit of the conduct.
EU site and office service for pharmaceutical companies
Advice and support for setting up an EU site with office premises, virtual office, mailbox and reception service, GDP storage and medicinal product law authorisations.
Labelling of small batches for clinical trials
Labelling, initial and re-labelling of small batches of investigational medicinal products, including printing of simple labels and processing of delivered labels and booklets.
Primary packaging and storage under GMP/GDP conditions
Primary packaging and sampling of solid medicinal products and active substances in a cleanroom environment as well as GMP/GDP-compliant storage across different temperature ranges.
Reviews

Aggregated rating

Aggregated rating
5
of 5

Aggregated from 2 reviews across all connected sources

Sources
GGoogle52
★TrustpilotSoon
PProvenExpertSoon

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Location

Lörracherstrasse 60
4125 Riehen
Opening hours
Mon
08:30 - 16:30
Tue
08:30 - 16:30
Wed
08:30 - 16:30
Thu
08:30 - 16:30
Fri
08:30 - 16:30
Sat
Closed
Sun
Closed

At a glance

Legal form
Limited Liability Company
UID
CHE-170.939.319
Founded
2012 · 14 years
Last commercial register change
September 15, 2026
Employees
21 to 50

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