What is level of certification?
What is the minimum manufacturing volume?
What information is made available to clients?
How long does it take to change a manufacturing site?
Which countries are currently supplied by Pharma Industries?
What is level of certification?
The facilities operate in accordance with "cGMP" (current good manufacturing practice) and are certified by all FDA-equivalent local authorities in the destinations where finished products are exported. Our operation is subject to quality audits by our clients at least once a year.
What is the minimum manufacturing volume?
| |
Minimum batch |
Maximum batch |
| Dry products |
200,000 tablets |
2,000,000 tablets |
| Capsules |
200,000 capsules |
2,000,000 capsules |
| Liquids |
500 liters |
2,000 liters |
| Cream & ointment |
100 kg |
150 kg |
| Sterile |
25 liters |
200 liters |
| Note: Start-up costs (US$ 5k - 30k) are incurred to cover stability, validation pilot batch procedures. |
What information is made available to clients?
Currently www.zip-online.com provides the following information online:
- Batch status report
- Service level
- Inventory information
Other key reports include:
- Batch record
- Inventory movement
- QA summary report
- QA deviation report
How long does it take to change a manufacturing site?
| < 6 months |
Australia, New Zealand, Singapore |
| 6-12 months |
Malaysia, Hong Kong, Vietnam |
| 12-24 months |
Philippines, Thailand, Taiwan, Japan, Korea |
Which countries are currently supplied by Pharma Industries?
- Japan
- Hong Kong
- Thailand
- Vietnam
- Malaysia
- Myanmar
- Cambodia
- Singapore
Note:
If there is any other area of interest not covered by these questions or other sections of
this website, please send your query to
contact@pharmaindustries.com
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