Regulatory Services

We support you with strategies, procedures,  can help you with meeting key stakeholders and securing the success of your product.  Further Services in this field:

Clinical Services

We provide high-quality advice tailored to your product on its way to approval by connecting the necessities of clinical development with the regulatory requirements.

Due Diligence

We generate independent and high-quality due diligence reports thus providing a confidential, unbiased perspective.

 

Your decision-making and negotiation processes will benefit from our expertise in GCP and our broad experience in regulatory decision-making.

Why choose
Coneckt consulting?

Over 25 years, Dr. Eckhardt gained in-depth expertise and broad experience in clinical drug development and regulatory affairs in multiple positions in academia (IKP, Stuttgart), at regulatory agencies (BfArM, EMA), pharma (Schwarz Pharma) and biotech (UCB Biosciences).

Since 2005, Dr. Eckhardt is lecturing in the Clinical Module in the renowned Master’s degree program in Drug Regulatory Affairs (MDRA) at the University of Bonn / German Society of Regulatory Affairs (DGRA).

He is author of more than 20 peer-reviewed publications.

Find out more
contact-coneckt-consulting-medical-due-diligence-drug-development
medical-consulting-drug-development-eckhardt

Medical & Regulatory Consulting

With more than 25 years of experience, we are experts in all areas of medication approval and can help you to publish your drug worldwide, hasslefree.

Our services include:

Find out more about us

Request a call back
and talk to an expert!

Fill out the form.
We will call you back shortly: