Commercialising Pharma & Medtech
Helping you navigate the regulatory landscape
We specialise in –
Solving regulatory & quality problems
for pharma & medtech.
Collectively our firm has over 80 years of experience supporting the commercialisation of pharma and medtech products.
Our Experts
Our reputable, talented team members are among the top in their respective fields.
We care about our clients and the broader healthcare community and will work tirelessly to achieve exceptional results for you.
Jeanette Lodge
BSc, Grad DipBiotech, MMedSc (Drug Development)
Director – Principal Consultant,
Founder of Mister Wolf Consulting
Anita Keith
BAppSc (Nutrition)
Senior Consultant
Greg Pearce
BPharm, Dip Hosp Pharm, PhD
Senior Consultant
Blog
Literature based registration submissions (LBS) an opportunity for your company?
Have you considered using a Literature Based submission (LBS) to extend the registration conditions …
Medical devices – it’s not always straightforward
It can be a little daunting, confusing, or even just time-consuming when your product doesn’t fit …
Designations and determinations
While planning a clinical program it is valuable to consider the designations and determinations …
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Schedule a no-cost consultation today!
Please contact Jeanette if you wish to discuss your upcoming project and how Mister Wolf Consulting might be able to assist.
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