A Queensland based consulting company
established in 2005 by Anne Jones, our principal
Quality and Regulatory Consultant and Director.
Acrapack is committed to supporting companies
in the medical, lifescience, biotechnology
and healthcare industriesand to maintaining
high consulting standards by providing complete
solutions for Quality, Regulatory and Compliance
challenges
We provide regulatory and quality assistance
on registration and compliance requirements
for Medical Devices, Invitro Diagnostics
(IVDs), Food, Cosmetics, and Medicines.
Anne is an experienced scientific and technical
affairs specialist, with 25 years management
experience and an exceptional track record
in delivering high level quality and regulatory
systems in the healthcare industry, with
a sound regulatory knowledge from development
to post market.
With knowledge of the critical aspects of
business which influence product quality
and compliance, Anne is particularly committed
to ensuring efficient development of processes
and quality designed productsto achieve
a balance between risk and commercial rewards
and ensure the Quality Management System
supports the business needs as well as meets
regulatory compliance.
Regulatory
Affairs and ISO 13485 expert
"Anne is a knowledgeable regulatory
affairs person who also is an expert
in ISO 13485. These two combine to make
her very desirable when it comes to
working with both Australian and overseas
manufacturers and distributors."
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