Pharma
Chelab is provided with a GMP facility (about 1500 mq) dedicated to qualitiy control of medicinal products.
The structure has been authorized by AIFA and by the Italian Ministry of Health for chemical/physical, biological and microbiological controls on:
- Medicinal products for human use, also for experimental use
- Medicinal products for veterinary use
- Pharmacologically active raw materials for human and veterinary use
The facility is equipped with:
- Laboratories of analytical chemistry
- Laboratories of physical chemistry
- Stability chambers
- Laboratory of microbiology provided with the following utilities
- Clean room dedicated to stability tests
- Clean room dedicated to bioburden tests
- Rooms classified as Biosafety Level 2 for tests with pathogens
- Rooms classified as Biosafety Level 3 for assays on viral agents
- Rooms for other microbiological analysis
- Rooms for LAL test
- Laboratory of molecular biology
- Laboratory of cellular biology
Chelab is equipped with state-of-art instrumentation in compliance with GMP.
In this facility many services for pharmaceutical companies and producers of API are performed.
The pharmaceutical division presents itself to the pharmaceutical companies with the best requisites in terms of regulatory authorizations, utilities, analytical equipments and technical support, in order to become a reference laboratory for the outsourcing of analytical services.
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