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Quality Assurance Unit co-ordinates the Quality
Assurance System, which is developed by all Pharmaceutical Research Institute's staff. The main goal of the applied
Quality Policy is to gain and retain our customers' credit through
services and products of the highest quality.
Our services and products' quality is
continually improving as a result of the constant advancement of processes, application of new research techniques,
employing highly educated and well-trained staff, continuous training as well as regular monitoring of processes and
studies.
All Quality Assurance Unit's activities are
based on the Pharmaceutical Law as well as Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP)
recommendations. The applied Quality Assurance System leads to constant improvement of reliability and guarantees
the fulfilment of our customers' requirements.
Quality Assurance Unit's main tasks include:
- Initiation and co-ordination of activities in the field of the Quality Assurance System.
- Close co-operation with research and manufacturing departments of PRI.
- Development and approval of system documents.
- Review and approval of quality training proposals, drafting and updating training schedules.
- Co-ordination of external audits.
- Preparation and execution of internal audits.
- Preparation of Quality Assurance System reviews.
- Supervision of corrective actions.
- Supervision of qualification and validation activities.
Staff:
- Scientific staff - 4 persons
| Contact: |
Dorota Samson-Lazinska, M.Sc. |
| Phone: |
(+48 22) 456 38 91 |
| Fax: |
(+48 22) 456 38 38 |
| E-mail: |
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