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MFI is a computational chemistry company specializing in drug discovery, quantum mechanics, molecular dynamics, cheminformatics, and artificial intelligence. Offering proprietary software, algorithms, and contract research services, MFI collaborates with organizations to accelerate preclinical drug discovery for small molecules, from biotech startups to established pharmaceutical companies.
We accelerate RNA-based therapy development. Nanofacile, a Montreal-based biotech startup, develops innovative RNA encapsulation solutions. Leveraging leading innovation hubs, the company aims to make RNA research and therapies more accessible and effective.
CRO services supporting grants, financial/budget structures, startup implementation, strategic planning, partnerships & alliances, annual reporting, regulatory affairs, preclinical/clinical studies – customized boutique services.
A multinational quality and compliance services group for life sciences companies, specializing in data integrity, digital governance, engineering and qualification, quality and compliance, regulatory affairs, lab excellence, pharmacovigilance, audits, and training.
CRO/CDMO providing development and bioproduction services for biological tools and raw materials required in cell therapy, gene therapy, immunotherapy programs, and other projects needing plasmid DNA, monoclonal antibodies, or recombinant proteins. RD-Biotech is a French biotech with over 20 years of expertise.
A pharmaceutical company providing CDMO, CMO, and bioanalytical services, including TK/PK reporting.
Seriant, a division of the Montreal Heart Institute, is a clinical research organization that provides comprehensive services to the pharmaceutical, medical device, and biotechnology industries, as well as to the academic community. Based in Montreal, Seriant operates internationally, supporting Phase I to IV clinical trials across a wide range of therapeutic areas. With our proven expertise in the development of innovative therapies, we help make a meaningful impact on people’s lives around the world.
Scimega is a Canadian clinical research organization specializing in oncology, conducting cutting-edge oncology trials for medium and small biotech companies globally. With expertise in collaboration with suppliers, Scimega ensures fast site start-up and optimal patient recruitment without compromising data quality. Its operational design is robust enough to adapt to evolving clinical trial environments.
We provide advanced services in GMP/GCP analyses, formulation R&D, clinical manufacturing, and clinical research for pharmaceutical, biopharmaceutical, and medical device sectors. Our solutions cover biologics and small molecules throughout the full lifecycle: development, testing, regulatory support, safety studies, clinical development, commercial QC, and post-market testing.
Sorintellis leverages explainable AI to optimize drug development, providing actionable insights for better, more confident decision-making. Sorintellis solutions target clinical trial risk management and pharmaceutical portfolio management, serving CROs, pharma/biotech companies, and life sciences investment funds.
PharmaLube develops LubriumMC, a high-performance lubricating biomaterial with potential applications in osteoarthritis treatment, dry eye, and other therapeutic, cosmetic, and industrial uses.
THEO Medical is an innovative player in pharmaceutical clinical research and the collection of blood products for research. We specialize in conducting clinical trials for pharmaceutical, biotechnology, and medical device companies.
MFI is a computational chemistry company specializing in drug discovery, quantum mechanics, molecular dynamics, cheminformatics, and artificial intelligence. Offering proprietary software, algorithms, and contract research services, MFI collaborates with organizations to accelerate preclinical drug discovery for small molecules, from biotech startups to established pharmaceutical companies.
Partnerships with NMX Research and Solutions (Quebec) and Oxeltis (France) to optimize research components related to drug design.
Computer-Aided Drug Design (CADD)
We accelerate RNA-based therapy development. Nanofacile, a Montreal-based biotech startup, develops innovative RNA encapsulation solutions. Leveraging leading innovation hubs, the company aims to make RNA research and therapies more accessible and effective.
Concordia University, McGill University
CRO services supporting grants, financial/budget structures, startup implementation, strategic planning, partnerships & alliances, annual reporting, regulatory affairs, preclinical/clinical studies – customized boutique services.
Academic institutions, health systems, research centers/institutes, biotechnology, medtech, biopharmaceutical, e-health, m-health
A multinational quality and compliance services group for life sciences companies, specializing in data integrity, digital governance, engineering and qualification, quality and compliance, regulatory affairs, lab excellence, pharmacovigilance, audits, and training.
International: QUINTIAN PHARMA, CQC (Glocal Quality Cannabis), Conceptio Provincial: BIOQuébec
ISO/IEC 27001:2022 Certified QMS ISO 9001
Commissioning, Qualification and Validation (CQV), Digital Governance, Audits
CRO/CDMO providing development and bioproduction services for biological tools and raw materials required in cell therapy, gene therapy, immunotherapy programs, and other projects needing plasmid DNA, monoclonal antibodies, or recombinant proteins. RD-Biotech is a French biotech with over 20 years of expertise.
ISO 9001
Engineering and production services for plasmid DNA (Research Grade to GMP), antibodies and recombinant proteins, raw materials within R&D programs up to clinical phases (DNA): RNA therapies, DNA therapies, viral vectors, CAR-T cells. Bioproduction, plasmid DNA, recombinant antibodies, CRO, CDMO
A pharmaceutical company providing CDMO, CMO, and bioanalytical services, including TK/PK reporting.
Support for drug discovery as well as preclinical and clinical development for over 50 biotechnology companies.
GLP, GCP, GMP SCC certified, FDA audited
Bioanalysis and TK/PK reports audited by the FDA and compliant with ICH M10 standards
Seriant, a division of the Montreal Heart Institute, is a clinical research organization that provides comprehensive services to the pharmaceutical, medical device, and biotechnology industries, as well as to the academic community. Based in Montreal, Seriant operates internationally, supporting Phase I to IV clinical trials across a wide range of therapeutic areas. With our proven expertise in the development of innovative therapies, we help make a meaningful impact on people’s lives around the world.
Several international partners.
Scimega is a Canadian clinical research organization specializing in oncology, conducting cutting-edge oncology trials for medium and small biotech companies globally. With expertise in collaboration with suppliers, Scimega ensures fast site start-up and optimal patient recruitment without compromising data quality. Its operational design is robust enough to adapt to evolving clinical trial environments.
The LEAN Six Sigma Company, McPeak Sirois, SPharm
Site selection and accelerated study start-up; provincial ethics approval strategy; Health Canada regulatory strategy; country monitoring; audit and GCP compliance consulting; full range of Scimega360 services
We provide advanced services in GMP/GCP analyses, formulation R&D, clinical manufacturing, and clinical research for pharmaceutical, biopharmaceutical, and medical device sectors. Our solutions cover biologics and small molecules throughout the full lifecycle: development, testing, regulatory support, safety studies, clinical development, commercial QC, and post-market testing.
PSD, LSO, BIOQuébec, PDA
GMP, GLP, ISO 17025
Sorintellis leverages explainable AI to optimize drug development, providing actionable insights for better, more confident decision-making. Sorintellis solutions target clinical trial risk management and pharmaceutical portfolio management, serving CROs, pharma/biotech companies, and life sciences investment funds.
The Sorintellis platform allows users to input various data and generate accurate forecasts on clinical trial success probability. A priori forecasting of trial performance can help sponsors avoid failures or delays due to preventable events. Additionally, explainable machine learning used by the platform anticipates future events and enables appropriate corrective actions to mitigate risks during clinical trial planning and execution. Our solutions are targeted to Contract Research Organizations (CROs), pharmaceutical and biotech companies, and life sciences investment funds.
PharmaLube develops LubriumMC, a high-performance lubricating biomaterial with potential applications in osteoarthritis treatment, dry eye, and other therapeutic, cosmetic, and industrial uses.
THEO Medical is an innovative player in pharmaceutical clinical research and the collection of blood products for research. We specialize in conducting clinical trials for pharmaceutical, biotechnology, and medical device companies.
Collection of blood products (blood, serum, plasma, cells)
Contact sponsors@clinicaltrialsquebec.com.
Follow the latest news from CATALIS and Clinical Trials Quebec
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