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Design

According to the principles of GEP
Based on good communication with the customer

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Qualification and validation

Efficiently, without unnecessary costs

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Consulting

Offer of solutions in accordance with GMP

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E-learning

Practical experience

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Personnel training

Practical examples and interactive workshops
Directly at the customer's site

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GMP audits

Preparation for the audit of state authority (SÚKL, FDA) or customer
implementation of audits

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Pharmaceutical quality system

Implementation and consulting
GAP analysis of set PQS

News

REGULATIONS MUST NOT BLOCK COMMON SENSE!!! company motto

About Pharm Partners

Pharm Partners is a modern design, engineering and consulting company focused on pharmacy and healthcare.

We come out of recent practical experience in the pharmaceutical industry and follow the methodology of GEP based on ISPE guidelines.

Our services meet the high demands of pharmaceutical production and GMP requirements (EU+US).

We are engaged in the activities from designing and delivery up to personnel training in GMP principles in a new functional and validated operation.

Pharm Partners is a limited liability company established in the year 2010 and based on the activities of persons originating from the former Pliva-Lachema (Barr) in Brno, who occupied various positions in manufacturing, engineering, maintenance, QA, QC, RA (e.g. managers, executives, specialists, process engineers, technologists and technicians). We continuously hire specialists - designers and top experts in pharmaceutical technologies. We have an expert for your particular problem and we will jointly find solutions to meet the current cGMP requirements (EU+US). We offer our experience in the manufacture of APIs, tablets, injection and infusion products manufactured aseptically or sterilized terminally. We have been improving our knowledge in foreign training courses and developing acquired skills in practice, when working with clients.

We would like to approach you with our offer of services that can meet the high demands of routine pharmaceutical production and the ever-increasing requirements for the implementation of new projects.

Selected references