We have over 200 pharmaceutical consultants covering the drug development life cycle - including drug discovery, preclinical drug development, clinical development, CMC, regulatory strategy and submissions, and commercialization.
Here are just a few examples of the kinds of requests CECON scientific consultants fulfill for pharmaceutical clients:
- I need help writing regulatory submission documents.
- I need a consultant to help prepare for a cGMC audit.
- I need input on a pricing strategy for a pharmaceutical product.
- I need someone experienced in interacting with FDA personnel on bio-statistical issues.
- I'm developing a biologic, and I need an expert to assist in the selection and qualification of a container and closure system.
Following are selected experts by area of specialty. You can find related experts in our proprietary data base. Scan the list, perform a key word search, or contact CECON. A member of our staff of PhDs will locate, vet, and introduce consultants to you based on your precise requirements.