Experience

The ClinPharmCologne team can look back on almost 20 years of experience in performing clinical trials. We are highly experienced in their

• Planning
• Execution and
  
• Evaluation

Our clinical pharmacologists have amassed a great deal of knowledge through many years of project management in both national and international research and development teams. You now stand to benefit from this experience.

We provide support in the following areas:

• in the pre-clinical phase (evaluation of pre-clinical results)
• throughout the entire spectrum of Phase I studies
• in Phase II (proof of principle) trials
• during the approval phase (preparation of clinico-pharmacological dossiers)

We also specialise in scientific research, as well as in the fostering and further development of a wide range of clinico-pharmacological methods and surrogates.

We also provide the following services:

• Monitoring
• Auditing
• Procurement of study nurses
• Medical writing
• Drawing up of development plans
• Evaluation of licensed products
• Biometric planning and evaluation (in cooperation with reliable, audited partners)

Benefit from our experience. We will be delighted to help you carry out your trials or research.


Examples of our experience in detail

Types of trial:

• ADME trials
• Bioavailability studies
• Bioequivalence studies
• Interaction studies
• Food-effect
• First-in-man trials
• Pharmacodynamic trials
• Studies in specific populations:

• the elderly
• sterilised women
• post-menopausal women
• smokers / non-smokers

• Patient studies, e. g. on erectile dysfunction
• “POC” studies

Studies involving different pharmaceutical preparations:

• Oral pharmaceutical products
• Ointments
• Patches
• Parenterals

Indications:

• Cardiovascular medicine
• Hemostaseology
• CNS
• Infection
• Pulmonology
• Endocrinology
• Urology
• Studies involving anaesthetics