What we offer:
We have on our books a comprehensive capability of professional staff accustomed to working to the TGA, FDA and Medsafe requirements:
Chemists experienced in Laboratory Instrumentation, LIMS, Method Validation to the FDA and TGA regulatory requirements.
Technical Document Writers, experienced in the Pharmaceutical, Biotechnology and Medical Device industries and writing up validation protocols.
Engineers, experienced in the pharmaceutical and medical device environment in various engineering disciplines to perform your validation cost effectively.
Process Validation Technicians experienced in process validation.
We have a "can do" attitude and looking for variety and challenges beyond the daily grind, so if you have a tough problem we are confident to supply the right person at short notice. No assignment will be too short or too complex.
All this at very affordable rates.
How it works:
You simply phone or email us with your requirement and we will response with suitable staff within days.
Head quartered in Melbourne, Australia, we operate through Australia, New Zealand, South Africa and South East Asia.


Contracted Autoclave Validation