Our range of services for your success
Specialist expertise is essential when it comes to the rapid and efficient realization of a research project in the field of respiratory tract infections. As an experienced Contract Research Organization (CRO), we offer you tailor-made support in the planning, implementation and evaluation of clinical studies on respiratory tract infections according to the highest quality standards and in compliance with all regulatory requirements.
Our proven expertise and experience in the field of respiratory diseases ensure that your products reach the market faster and more efficiently. In addition, our customized study designs, efficient patient recruitment and stringent study management. We utilize state-of-the-art technologies for accurate data management and provide professional reporting to ensure that all regulatory requirements are met.
Customized study design for respiratory diseases
Careful planning is crucial for the success of clinical trials on respiratory infections. Experts create precise study protocols taking into account the specific challenges of respiratory diseases.
This includes:
- Definition of suitable inclusion and exclusion criteria
- Selection of relevant endpoints such as lung function or symptom scores
- Determination of adequate treatment periods and follow-up periods
- Consideration of seasonal fluctuations in respiratory infections
Efficient subject recruitment
Efficient patient recruitment is essential for the success of clinical trials on respiratory tract infections. We develop targeted strategies:
- Analysis of the target population based on inclusion criteria
- Cooperation with specialists and general practitioners
- Targeted advertising campaigns during cold and flu seasons
- Use of patient registries for chronic respiratory diseases
- Educational materials on study objectives and potential benefits
Efficient project management
Conducting clinical studies on respiratory diseases on time and within budget. Experienced project managers coordinate all aspects of the study and act as a central point of contact. We ensure seamless integration of all sub-areas and offer:
- Structured planning and implementation of the study
- Transparent communication with the parties involved
- Flexible resource management
- Fast response to unforeseen events
Precise data management
State-of-the-art technologies for accurate recording and analysis of parameters.
Clinical monitoring in respiratory tract infection studies
Monitoring ensures the quality and integrity of the data collected in respiratory tract infection studies. We offer:
- On-site visits to check that lung function tests are being carried out correctly
- Remote monitoring for prompt review of symptom diaries
- Central monitoring to identify trends
- Training for investigators on the standardized recording of respiratory symptoms
Professional reporting
Evaluation of long-term use uOur experts create clear and meaningful documentation of your study results, specifically tailored to respiratory tract infections. We take into account all relevant parameters such as lung function values, symptom scores and microbiological data. Our reports not only fulfill regulatory requirements, but also provide valuable insights into the efficacy and safety of your therapy. We use state-of-the-art statistical methods to adequately account for seasonal effects and other characteristics of respiratory infections. We also ensure that all data is collected and presented in a GCP-compliant manner to ensure smooth submission to authorities.nd Safety requires specific approaches:
- Conducting long-term studies to record chronic effects
- Systematic recording and evaluation of undesirable effects
- Consideration of possible interactions with long-term use
Regulatory support taking into account specific requirements
Our team accompanies you through all regulatory procedures, from the initial application to the final approval of your therapy for respiratory infections. We are familiar with the specific regulatory requirements for studies on respiratory diseases and take these into account from the very beginning of study planning. This includes the selection of suitable endpoints, the definition of safety parameters and the consideration of potential interactions with other drugs. We support you in communicating with authorities and prepare you optimally for possible queries. Our aim is to make the approval process for your respiratory therapy as efficient as possible and to identify and address potential obstacles at an early stage.
Place your trust in our expertise
Benefit from our specialized experience in the field of respiratory infections. We know the challenges and special features of clinical trials for respiratory diseases and have already successfully completed numerous projects. Our expertise includes both viral and bacterial respiratory infections as well as chronic lung diseases such as COPD.
Locations
Maps
contact@mediconomics.com
+49 (0) 511 560 998-0
Call us
And what can we do for you?
Dr. (MD) Uwe Albrecht,
FIBMS, FFPM (Dis.), FICR, CSci
CEO
Headquarters
Hanover
FAQ – frequently asked questions
Yes, we have experience in conducting multinational studies and have an international network. We know the country-specific requirements and can coordinate your study efficiently across national borders.
We offer:
- In-depth specialist knowledge of respiratory diseases
- Experience with seasonal fluctuations in infectious diseases
- Optimized processes for conducting airway studies
- Access to a network of experts and test centers
- More efficient study processes thanks to specific expertise
Typical challenges are
- Seasonal fluctuations in the incidence of infections
- Rapid recruitment during acute waves of infection
- Consideration of comorbidities and pre-existing conditions
- Compliance with strict hygiene and infection protection measures