Our comprehensible packages
We Focus on Your Efficiency
From consulting to multi-year clinical studies – we have the right package for everyone.
Customised Solutions for Your Clinical Challenges
Choose from four packages with different scopes of services and receive targeted support for every phase of your project. We accompany you from the initial analysis through to implementation – transparently, flexibly and practically.
Would you prefer a customised package with modular services? No problem – just contact us.
Large
you acquire the carefree package. Not only do we plan a clinical trial (both for market approvals and PMCF), we also carry out the trial, from biometrics and safety to communication with the authorities.
This is our core skill and our USP: thanks to our excellent network and our knowledgeable staff, multicenter, international clinical trials are what we do best. Our USP thanks to our
excellent network.
Medium
medical and/or IVD products who wish to make targeted use
of services to prepare for a clinical trial.
In contrast with the large package, however, we do not conduct studies within the medium-sized package, but provide you with comprehensive support in planning, strategy and the necessary preparations.
Small
of medical and/or IVD products. With the literature analysis (SOTA), we pave the way for a successful clinical or performance evaluation, for which we prepare both the plan and the report.
On request, we can supplement the package with a comprehensive literature search that brings together relevant scientific data and findings.
Intro
you need to collect clinical data? Whether you are a start-up,
an SME or a corporation, book our intro Package – we will provide clarity.
With our intro package, you receive our in-depth consulting, combined with a literature search, so you can make informed decisions based on a solid data foundation.
Your Contact for all Questions
I will be happy to support you and forward your request to the to the right experts.
Send me an e-mail or give me a call – I look forward to hearing from you.
Package request
Choose Your Package – we Take Care of the Rest
We make sure that all interfaces are defined and considered. With us, you will always be up to date.
FAQs
You can find more details in the package overview and a brief description. Are you still unsure? Contact us.
Our services cover a broad range – from in-depth consulting to multi-year, multicenter, international clinical studies. You can find an overview of our packages here.
Yes, our focus on the most efficient solution for you and your product.
We are ISO 13485 certified and cover both MDR 2017/745 and IVDR 2017/746. Nothing stands in the way of an application to the ethics committee and market approval.
Our services primarily address the EU market, but we also provide services for overseas markets. Just ask us!
While the intro package is completed within a few days, the large, most comprehensive package can take several years.
Do you have a specific question? Ask us, give us a few key points and we will estimate the scope for you.