ALTIORA is a peoples business
• is a mid-sized Contract Research Organisation (CRO), driven by successful organic growth.
• has been developing its expertise for almost 20 years, working on local and large international projects in the EU countries.
• has a team comprised of trained and experienced professionals, focused on providing high quality services, without the high fixed costs of a conventional large full service CRO.
• provides a comprehensive array of clinical trial management services. Our expertise includes the following services:
- Medical Writing
- Medical Affairs
- Clinical Operations
- Regulatory Affairs
- Quality Assurance & Training
- Data Management
- Central ECG & Respiratory reading
- Central Lab
- Pre-clinical Research Modelling, Chemistry, Bio-analysis and Toxicology
HOW WE DO IT!
What we want to accomplish?
Our vision is to help and assist our clients moving through the clinical research phase all the way to registration the same way as they would do by using their own R&D, with ultimate vision to bring satisfaction to patients and healthcare professionals, which leads to overall benefit to public health.
How to reach our goal?
provide tailor made clinical research services to biotech and pharma companies in order to move their product through research phase.
share and complement biotech and pharma companies with the knowledge, experience and resources.
provide biotech and pharma companies with efficient, straightforward and quality service, information or advice.
be flexible and adapt quickly to clients’ needs.
What we value?
teamwork and collaboration, respect, commitment and passion.
knowledge sharing culture.
easy and practical management and administration.
open and straightforward communication.
HOW WE DO IT!
Altiora has the capability to take complete management of global clinical development programs.
Over the course of many successful international projects, Altiora has developed a set of best practices that ensure increased management efficiency.
Quality assurance and training
The Quality Assurance Department is an independent department of Altiora, and is responsible for maintaining and monitoring the quality of all our work.
As a part of our clinical trial services, we provide independent reviews and audits of clinical trial investigator sites, research groups and sponsor clinical operations, to ensure compliance with Good Clinical Practice (ICH-GCP), as well as EU and local regulatory standards.
Our Business Development unit provides access to Altiora staff and consultants with expertise in business development and negotiating contracts, to ensure that all budgets and contracts are negotiated and executed in line with best practice.
Altiora’s internal Clinical Science Group is strengthened using external experts, to enable us to provide our clients with expertise and support in protocol design, medical writing and medical monitoring.
Altiora has extensive experience in studies across multiple therapeutic areas. Our experience covers many different indications and studies of varying sizes - from the perspective of both number of sites and number of patients.
The pie chart illustrates our experience across various therapeutic areas.
What do we want to accomplish?
Altiora’s goal is to help and assist our clients moving through the clinical research phase, all the way to registration. We aim to mirror the way in which our clients use their own R&D, with the ultimate vision of bringing satisfaction to patients and healthcare professionals alike, leading to an overall public health benefit.
How to reach that goal?
Provide tailor-made clinical research services to biotech and pharma companies in order to move product(s) quickly through research phases.
Share and complement biotech and pharma companies' knowledge, experience and resources.
Provide biotech and pharma companies with efficient, straightforward and quality service, information and advice.
Be flexible and adapt quickly to clients’ needs.
What do we value?
Teamwork and collaboration, respect, commitment and passion.
Knowledge sharing culture.
Easy and practical management and administration.
Open and straightforward communication.