Lehrman Biopharma consulting has accomplished the
following:
Past successes / Current partners
Enhanced the bioavailability and increased in vivo half-life by
modifying protein structure and small molecule salt form.  
Screened and selected formulations for proteins and small
molecule drug candidates.  Several of these modified
candidates and formulations are currently in clinical trials.
Developed robust analytical methods for final product
characterization and stability testing.  In some cases, these
methods have been transferred to contract laboratories.
Selected and managed contract organizations that have
manufactured cGMP compliant drug substance and drug
product.
Authored documents in support of regulatory filings.
AAPS Newsmagazine article on protein aggregation
Of special interest:
Protein aggregation is a critical concern to companies that
are developing biotechnology-derived drugs.  Russ has
significant experience and expertize in this area.  Check his
recent article on this topic: