GMP / GDP Consulting.

With our consulting package for operating procedures that comply with regulations, we make you fit for the future.


Produce your products in accordance with GMP.


Stand up to any audit.


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Case Study.

Implementation of EU GMP regulations for GMP analytical QC testing.

Analytical / bioanalytical quality control (QC) tests for medicinal products / biologics are a "manufacturing step" and require GMP certification. Expand the scope of analytical / bioanalytical testing to QC of drugs / biologics as a service for drug / biologics manufacturers. QMS certified according to GLP and ISO 17025, but EU GMP regulations cannot be met. Lack of adequate resources with required GMP knowledge as main problem in GMP implementation.
Insufficient prior and internal GMP knowledge necessitates re-creation and updating of existing quality documents to broaden the scope and adopt processes of existing standards to meet GMP compliance and ensure NCA inspection readiness.


  • Implementation of an overall GMP-compliant quality management system, processes and standards
  • Implementation of an adequate GMP-compliant device qualification process
  • Implementation of GMP-compliant method and process validations, efficiency measurements and control systems (in-process controls, IPCs)
  • Preparation of the documentation required by EUDRALEX Vol 4, such as the Site Master File (SMF, Part III).
  • Achieve EU GMP compliance and National Competent Authority (NCA) inspection readiness.
  • Establishment of a comprehensive communication control / communication loop leading to continuous improvements

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What is GMP?
Good Manufacturing Practice (GMP) refers to the minimum standard that pharmaceutical manufacturers must adhere to in their production processes. To comply with these standards, the European Medicines Agency (EMA) coordinates inspections to these standards and plays a key role in harmonising GMP activities at the European Union (EU) level. Manufacturers whose medicines are destined for the EU market must comply with GMP, regardless of where the medicines are manufactured. GMP requires that medicinal products:
  • are of consistently high quality;
  • are suitable for their intended use;
  • meet the requirements of the marketing authorisation or the clinical trial authorisation.

The principles of Good Laboratory Practice(GLP) define a set of rules and criteria for a quality assurance system that addresses the organisational process and conditions under which non-clinical health and environmental safety testing is planned, performed, monitored, recorded, reported and archived.