Vyridis AG in Switzerland offers Quality Management Services to help customer comply with international regulations, especially in the pharmaceutical sector.
This service includes QA, QP services through advisory, temporary or long term staffing, quality audits and training. It can be extended to QC testing via partner laboratories.
Quality Management Advisory/Operational Services
These services include quality management, quality control and quality assurance services. Professional advisory is provided on implementing good practice guidelines and ensuring compliance.
GxP Services
Pharmaceutical quality management system cover all aspects of a product’s life cycle, from development to patient use, where the Quality Assurance measures are implemented at each step of the cycle.
We develop a complete GxP quality management systems and provide advisory services on quality assurance, i.e. the support is provided to pharmaceutical companies and their QPs by integrating the required standards into their quality management systems, according to GxP guidelines, demonstrating compliance to regulatory agencies during audits & inspections.
Audits & Training
In order to contribute to the knowledge development of the customer staff, secure compliance and help upgrade QMS systems, Vyridis is offering Training and Professional Audits as indicated in the table below:
Qualified Person – QP Services
QP service provides pharmaceutical companies with an experienced partner to support them in their compliance duties. The service can be provided temporarily to bridge the gap related to staff transitions or on PTO/holiday leave. Alternatively, the service can be deployed on a longer term basis by taking “ownership” further down of the Quality Management Process related to the manufacturers of medicinal products and investigational medicinal products. Such QP (Qualified Person) services include:
- Batch release and/or EU import release
- Batch review
- Product Quality Review (PQR)
- Performing GMP audits
- Performing internal audits
- Preparing for and guidance during inspections by the competent authorities
- Licence applications
- Drawing up procedures and contracts
- Establishing or fine-tuning a quality management system
