Pharma Industries

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 destinations where finished products are exported. All our operations are subject to quality audits by our clients at least once a year. In addition, Philippines and Vietnam plants are certified by the Australian TGA.

What is the minimum manufacturing volume?

Dry products	200,000 tablets
Capsules	200,000 capsules
Liquids	1,000 liters
Cream & ointment	100 kg
Sterile	10 liters
Penicillin / Cephalosporin	200,000 tablets
Note: Start-up costs (US$ 5k - 30k) are incurred to cover stability, validation pilot batch procedures.

What information is made available to clients?

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
Korea
China (via HK)
Taiwan
Hong Kong
Thailand
Vietnam
Malaysia
Singapore
Philippines
Australia

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