Do you need help with the regulatory processing of your clinical research project? Geistek Pharmaceuticals is your solution!

We have a highly specialized team with extensive experience in the regulatory processing of clinical research projects. Our goal is to help you obtain all the necessary authorizations to carry out your project quickly and efficiently, minimizing any delay or inconvenience.

In addition, we offer a completely personalized service tailored to your company’s needs. We will work closely with you to ensure that your project meets all the regulatory requirements and standards necessary for approval.

Please do not hesitate to contact us for more information on how we can help you to efficiently and successfully process your clinical research project. Geistek Pharmaceuticals is committed to supporting you at all stages of your research project!


The regulatory processing of clinical research projects involves several important steps, including:

1. Obtaining ethics clearance

It is necessary to obtain ethics clearance from the appropriate ethics committee to conduct the clinical research project. This includes review and approval of the study protocol and informed consent information.

2. Obtain regulatory approval

Depending on the country in which the study is being conducted, we will take the necessary actions to obtain regulatory approval from the appropriate health authorities to conduct the project.

3. Registering the study

We will register the study in the relevant databases, such as in the United States or EudraCT in the European Union.

4. Obtaining the necessary permissions

We will obtain special permissions to carry out the clinical research project, such as research permits or data access permits.

5. Supervision and follow-up of the study

Once all the necessary authorizations have been obtained, we carry out an adequate monitoring and follow-up of the study to guarantee compliance with the protocols and regulatory standards.

It is important to bear in mind that the regulatory processing of clinical research projects is a complex process and requires a great deal of planning and attention to detail. Therefore, it is advisable to have the support and advice of experts in the field to ensure the success of the project.