Our Services
Drawing on our expertise and commitment to innovation, we provide you with a full range of services designed to ensure the success of your clinical trials.
Whether you need global support or targeted support at each stage of the process, we offer tailor-made solutions, always in accordance with the most demanding industry standards.
Our goal is to provide you with a quality service, optimized to guarantee reliable and efficient results.
Compliance
The CLIRE PHARM team understands that compliance with clinical trial standards is essential. As a CRO, here are a few key points we are committed to maintaining :
- ICH/CGP Certification : CLIRE PHARM adheres to internationally recognized Good Clinical Practice (ICH/GCP) standards to ensure the proper conduct of clinical trials – design, conduct, monitoring, and reporting – and patient safety.
- Ethical considerations : obtaining consent from trial subjects, protecting their rights and safety, and maintaining the highest standards of quality in the conduct of clinical research.
- Data integrity : CLIRE PHARM is an Algerian CRO that ensures that all clinical trial data is accurate, complete, and attributable. This includes secure data management and compliant storage of electronic records (21 CFR Part 11).
- Continuous improvement : we continuously improve by identifying areas for improvement in our processes, technologies, and staff skills, to ensure ongoing compliance and high-quality service delivery.
Training
To help you conduct your clinical trials in line with best clinical practice and international standards, our experts at CLIRE PHARM also offer skills development for staff involved in clinical research by transferring their know-how, including :
- Initial training : aimed at preparing professionals for their role in clinical research, CLIRE PHARM teaches the basic principles of good clinical practice (ICH/GCP), regulations, and criteria specific to clinical study protocols. Clinical Research Associates (CRAs) and Clinical Trial Coordinators (CTCs) receive the training they need to carry out their projects.
- Ongoing training : ongoing training is essential to ensure that staff are up to date with the latest industry standards, regulations, and technological advances. That’s why we offer regular training programs and updates to maintain the staff’s professional competence.
- ICH/GCP Training : CLIRE PHARM ensures compliance with ICH/GCP, protocol, data quality, and participant safety. ICH/GCP training is the key to ensuring that clinical trials are conducted in line with international standards.
CLIRE PHARM Algérie training courses include :
- Pharmaceutical industry principles and drug development processees.
- Basics of clinical trials.
- Study design.
- Essential Documents.
- Patient protection principles.
- Investigational product management.
- Transport and logistics.
- On-site storage and management.
- Return and disposal.
- Various monitoring visits.
- PSV (Pre-Study Visit).
- SIV (Site Initiation Visit).
- IMV (Site Initiation Visit).
- COV (Close-Out Visit).
- Medical and safety monitoring.
- Introduction.
- Assistance to sites and sponsors.
- AE/SAE (Adverse Events/Serious Adverse Events).
Support for the Pharmaceutical Industry and the Development of Innovative Treatments
CLIRE PHARM assists you in your production and biomedical research initiatives. We offer a wide range of services to help you achieve your goals :
- Market research : identifying opportunities for innovation is just as important as conducting clinical research projects – we carry out in-depth market research to understand the dynamics and needs of the healthcare market.
- Data collection : our team is dedicated to collecting, managing, and analyzing data for biomedical research. We ensure that data is collected ethically, legally, methodically, and in compliance with research protocols. Data integrity is preserved throughout the study.
- Marketing : implementation of marketing strategies, development of market access plans, and compliance with local and international regulations.
- Marketing Authorization (MA) : we can help you obtain marketing authorization for your medical products by assisting in the preparation of regulatory-compliant dossiers, interacting with regulatory authorities, and following up on applications until the necessary MA is obtained.
- Production : CLIRE PHARM iidentifies local pharmaceutical producers with the technical potential to meet your requirements and adapt to national and international market realities.
Phase I - IV Clinical Trials
In the complex field of biomedical research, excellence is not only a goal but a necessity.
CLIRE PHARM helps you to conduct your clinical studies rigorously through the various phases. We are committed to guaranteeing you the highest standards of service quality :
- Treatment durability : CLIRE PHARM works closely with its customers to ensure the long-term sustainability of their innovative drugs and molecules through the collection of accurate and meaningful data.
- Assistance through phases I – IV : from initiating studies to obtaining Marketing Authorization (MA), CLIRE PHARM is ready to help you manage clinical trials, submit data to regulatory authorities, and monitor key stages in the drug development process.
- Guaranteed efficiency : our priority is to prove that the drugs and treatments we support work. To do this, we set up robust studies. We collect accurate data and thoroughly analyze the results to ensure that treatments are effective.
- Ensuring safety : patient safety is a top priority. We implement rigorous safety monitoring processes throughout clinical studies to minimize risks and ensure the well-being of participants.
Contact Us
We are available to meet your needs. Contact us for personalized advice and tailored solutions.