|
Full list of services
To discuss your requirements or to request further information or a quotation, please contact us for more info.
Auditing and evaluation
- Supplier audit (cGMP, ISO9001:2000, PS9100:2002)
- Service Supplier audit (cGMP, ISO9001:2000, PS9100:2002)
- Internal audit (cGMP, ISO9001:2000, PS9100:2002, internal QMS)
- Evaluation of contract testing laboratories
Training
- Stability Testing procedures
- GxP for pharmaceutical QC and Development Laboratories
- GMP for Pharmaceutical Excipient Manufacturers
Validation
- Preparation of Validation Master Plans and associated documentation
- Qualification of manufacturing and testing equipment
- System and process validation
- Analytical method transfer
- Process transfer
- Qualification and validation of stability testing facilities
Stability testing
- Preparation of stability testing protocols
- Review and evaluation of stability test results
- Advice on specific dosage form requirements
- Preparation of stability reports
Consultancy
- Review of validation programme
- GMP review of stability testing facilities and procedures
- Review of training programmes
- Preparation of technical reports
- Statistical analysis of technical and manufacturing data
|
|
|
