Feeling secure requires knowledge and experience
When you look for a Clinical Research Partner, do you consider if your partner understand your business and priorities correctly?
- Do you focus on quality and time to market?
- Does budget control and early warnings means that you feel a reliable relationship with your partner?
- Is it crucial to your business that your partner understands your positions in the market?
- Do you prefer a partner, who can accelerate based on effective processes without losing focus on quality?
- Do you look for a partner, who can be flexible in scope from full control over the studies to partial studies?
If you recognize your business and way of working in the above, we seem to understand business the same way.
We have more than 20 years of experience and we are known in the market for a professional and dedicated approach to all assignments. The long-term relationships to our existing clients in the market are, to us, the best testament of that. Yet, we constantly challenge our methods, guidance and skills to develop our business approach to the benefit of your business.
Despite these online ages, we prefer to get to know each other in person. Collaborating in bringing a product to market requires good relations and trust. Accordingly, please don't hesitate in setting up a meeting.
Clinical Operation requires expertise, accuracy, and speed as it is essential for the drug to get to market as fast as possible in order for the pharmaceutical company to receive a return on their initial investment and patients the availability of new drugs and treatments
The key to success, when it comes to well-managed and -conducted clinical trials, is the implementation and execution of Quality Assurance (QA) principles throughout the lifetime of a trial. High- quality SOPs, processes that are thoroughly prepared and GcP principles are the foundation of which clinical trials should be buildt.
Both Statisticians and Data Managers are key people in the processing of reliable high-quality data and both must be involved in the project from the early planning to the final closing.
CroxxMed senior regulatory staff are used to navigating within cross-functional teams during the application process. Our regulatory team has extensive experience in advising, compiling, writing, and submitting applications and amendments to Competent Authorities as well as Ethics Committees.
We base our project management upon 5 essential processes: initiating, planning, executing, monitoring/controlling and closing. Project Managers at CroxxMed strive to manage your project, customized to your needs and desires.
Patient safety is a key component and imperative in all clinical trials – whether it’s drugs or devices and no matter how innovative, it cannot be registered and get to market unless proven to be safe. For all medicines, there is a trade-off between the benefits and the potential for harm.
In our line of work with its urgent deadlines,
close and active collaboration is essential for a successful result.