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 CMC documentation is critical to the success of your business?


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.