Pharmacokinetic advise:
Study design and protocol Phase I studies Metabolism Bioavailability Drug and food interaction

QA audits and management:
System audits for CRO's and Pharmaceutical Companies Specific study audits phase I – IV QA programs for companies

Regulatory advice:
Scientific advice with authorities Expert reports

Project management:
Phase I, PK/PD studies Clinical research Phase II-III studies Therapeutic equivalence studies Due Diligence Risk assessments

Medical writing and publications:
Protocols and study reports Bio-waivers

Special formulation advise:
Sustained release formulations Inhalers - Local application formulations

Training courses:
Bioavailability and equivalence Pharmacokinetics Quality assurance ICH/GCP Audits and company responsible GCP and GLP activities