QVA and GMP COMPLIANCE
Pharmaplan was founded more than four decades ago by a pharmaceutical manufacturer – GMP is therefore in our blood and we are happy to share our many years of experience with our customers in the pharmaceutical industry so that they can meet the constantly growing international quality requirements.
Qualification and Validation
Through close interdisciplinary cooperation with our Pharmaplan experts from project planning, engineering, and GMP compliance, we can offer our customers seamless qualification and validation services.
We support our customers in planning, assist in the development of qualification and validation strategies, advise on the current legal guidelines of the various countries and provide a complete documentation package. Our highly qualified employees complete complex workflows in compliance with GMP, even within limited time frames. In this way, we prepare our customers for the start of GMP-compliant production or upcoming inspections by the authorities.
Our Pharmaplan qualification experts have extensive experience with the quality systems of well-known pharmaceutical manufacturers but are of course flexible enough to develop solutions tailored to individual customer needs. In addition, access to the defined Pharmaplan internal quality system, which follows the risk-based approach and the verification model according to ASTME2500, allows processes to be accelerated.
Our specialists in the QVA area are competent contact persons for these areas:
>Risk analyses, GAP analyses
>IQ / OQ / PQ
>Media systems (water systems, HVAC, clean rooms)
>Qualification and validation of process plants (cycle development, temperature distribution studies)
>Computer system validation
GMP Compliance Consulting
The global regulatory environment is changing rapidly. It is a challenge for many companies to meet the increasing GMP requirements.
With our knowledge of the current international GMP regulations and the relevant industry standards, we help our customers to successfully pass inspections and audits and also provide support for technology transfers.
To guarantee GMP compliance in all functions and phases, we offer our customers consulting services throughout the entire product life cycle.
When introducing or optimizing a Quality Management System (QMS), we place great emphasis on the balance between regulatory requirements and practical operational needs. We know how to tailor our consulting services to small and medium-sized companies – without compromising quality.
Within the scope of process validations, we provide support in the creation of concepts and the necessary documentation, including SOPs.