Welcome to

Paar Pharma Consulting

Individual and and comprehensive advice in the GxP-regulated drug and active ingredient area.

Welcome to

Paar Pharma Consulting

Individual and and comprehensive advice in the GxP-regulated drug and active ingredient area.

Consulting

Consulting, analyses, interim management, quality assurance and planning in the GxP-regulated area

Certification

Assistance in preparation and review of applications for permits

Auditing

Assistance in preparation, implementation and follow-up of audits

Training

Training in all GxP-relevant and process-specific topics

Your powerful partner in the pharmaceutical industry

We offer you individual and comprehensive advice as well Support in GxP-regulated drug and active ingredient area, including in the areas of quality management, auditing, training and regulatory issues.
Reliability, accuracy and trust are our most important principles.
We provide clear, concrete assistance and solutions without hesitation and support you in your projects so that you can achieve your goals even faster and more effectively.

Areas of expertise:
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Establishment, testing and optimization of quality management systems (GMP, GDP, GCP)

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GAP analysis of systems in the GxP area and ensuring inspection readiness

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providing education programs

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planing and implementation of audits

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accompaniment of official inspections

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acquisition of permits (MIA/BtM/WDA) and certifications (GMP/GDP)

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assumption of responsible positions (QP/VPwholesale/BTM-V)

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assistance with regulatory questions

Your Partner in the pharmaceutical industry

Our services

We provide clear, concrete assistance and solution approaches outright and support you in your projects so that you can achieve your goals even faster.

DEVELOPMENT, TESTING, AND OPTIMIZATION OF QM-SYSTEMS

We support you in the development or expansion and optimization of your QM-System which is based on a comprehensive GAP-analysis, in order to establish a system tailored to your company and needs, in accordance with a cost-benefit-risk assessment.

MANUFACTURING AND WHOLESALE LICENSES, AS WELL AS GMP/GDP CERTIFICATES

We support you in obtaining and maintaining manufacturing licenses, wholesale licenses ad narcotic licenses, as well as in their modification or expansion.

REGULATORY ISSUES

We support you in processing and answering regulatory issues and situations in the pharmaceutical environment.

AUDITING IN GXP-RELEVANT AREAS

We support you with our educated auditors, who have several years of professional experience in various GxP-relevant areas, in planning, conducting and follow-up of external and internal audits (self-inspections).

IN-HOUSE AND VIRTUAL TRAININGS

We support you in the initial qualification and continuous training of your employees through individual in-house or online training courses on general or specific topics tailored to your needs.
Up to

15%

time-saving by optimizing your process workflow

THE SOLOUTION FOR YOUR STAFF SHORTAGES

Due to a lack of resources, bottlenecks often arise in various GxP-regulated areas of pharmaceutical companies.
As an external partner, we are available to you flexibly and provide our support together with comprehensive expertise to your company.

Our customers

Customers and partner who trust us

Through our many years of experience and qualifications, we are a trusted partner in the pharmaceutical industry, providing consulting services in the GxP-regulated drug and active ingredient sector.

Process workflows and case studies can be found here:
 

Our support

Do you need support or have questions?

Our team is at your disposal and will be happy to advise you on topics related to quality management systems, analyses, certifications, and regulatory issues.

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Free initial consultation

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Analysis & planning

Implementation & Training

From planning to execution

How we work

Our processes are precisely coordinated with each other, ensuring a smooth implementation process. We will guide you step by step through all relevant topics and provide you with individual and comprehensive advice.

who we are

Our team

Michael Paar

Michael Paar

Owner / Principal Consultant

Nadin Stramka

Nadin Stramka

Senior Consultant

Headquarters of the company
Am Schönblick 8
86482 Aystetten

Augsburg branch
Annastr. 15
86150 Augsburg
Mobil: +49 (0)178 - 206 23 30

E-Mail: kontakt@paar-pharma-consulting.com

Use our contact form directly

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