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?

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