Are
you a
manager in the pharmaceutical industry with responsibilities for GMP
auditing, CMC documentation or stability testing, but limited resources
to meet the
timelines?
Are you faced
with challenges due to variability in your development pipeline, and need to
decide whether to build up internal capacity or to manage the peaks and troughs
by means of external cooperation and outsourcing?
Do
you require assistance with the GMP auditing of CMOs and CROs or API,
raw material, excipient, packaging or medical device suppliers for
Human Pharma or Veterinary products?
Do you need help writing stability reports and compiling CMC documentation for worldwide submission?
Are you
uncertain whether to outsource this work because the quality of the
Would your
‘ideal consultant’ be someone who understands the pharmaceutical business, from
the inside, with significant experience working in the pharmaceutical industry?
If the answer to
any of
these questions is ‘yes’, then please take a look at the services
we offer.
For more information, or
to discuss your particular requirements, please contact
us by phone
or email.
