List of Contract Research Companies in Canada - 27

Founded in 2017, 48Hour Discovery (48HD) has a powerful technology platform for peptide-based drug discovery. We are reducing the cost, time, and risk of developing new therapies with our innovative target screening strategy to quickly identify the best and most promising drug leads.

AbCellera is a technology company that searches, decodes, and analyzes natural immune systems to find antibodies that its partners can develop into drugs to prevent and treat disease. AbCellera partners with drug developers of all sizes, from large pharmaceutical to small biotechnology companies, empowering them to move quickly, reduce cost, and tackle the toughest problems in drug development. For more information, visit www.abcellera.com.

Acuitas is the premier LNP (lipid nanoparticle) technology provider, enabling our partners to advance new therapeutics to address unmet clinical needs. We have developed a broad IP portfolio focussed on the use of LNP technology for nucleic acid therapeutics. This portfolio primarily encompasses novel compositions of matter but also includes novel uses of nucleic acids therapeutics. Our mission is · To provide our partners with the best LNP delivery technology for nucleic acid therapeutics · To support our partners to rapidly advance new therapeutics to address unmet medical needs · To continually innovate to maintain and strengthen our LNP technological lead Acuitas partners locally and globally with companies, academic institutes and other organizations to improve human health.

AcuPharma is a Canadian based company that provides a wide range of services for pharmaceutical and biotech partners. Our aim is to assist our clients in reaching their goals by providing chemistry expertise, as well as contract research and custom synthesis.

Affinity Biologicals Inc. is a biotechnology company based in Ancaster, Ontario, Canada, specializing in hemostasis diagnostics and research. Founded in 1987, the company develops, manufactures, and markets over 250 high-quality reagents and kits used in coagulation and thrombosis studies. Their product offerings include coagulation-related antibodies, matched-pair antibody sets for ELISA, depleted/deficient plasmas, and a line of complete ELISA kits. The company also provides tailored services such as research and development, custom manufacturing, and contract services to support clients in the biotechnology and healthcare sectors. Affinity Biologicals maintains a strong commitment to quality, operating under an ISO 13485:2003 registered Quality System and holding licenses from regulatory authorities like the US FDA and Health Canada. With a dedicated team of around 30 employees, Affinity Biologicals serves a global market through a network of distributors.

Outsourcing made easy with a one-stop solution to early phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

We are a Canada Based Contract Research Organization with expertise in contract research, custom synthesis, analytical services, and drug development. We support all your research needs by reducing the project timeline and cost.

Welcome to Biomatik - Your Quality Source of Integrated Products & Services for Life Sciences and Drug Discovery! ​Biomatik has been proudly serving the life sciences and drug discovery industry since 2002. In the first 10 years, Biomatik had been primarily focusing on Biochemicals, Gene Synthesis, and Peptide Synthesis. In the past 5 years, Biomatik has largely outgrown the above product lines and is rapidly expanding its new product lines: ELISA Kits, Proteins, and Antibodies. Offered Products: 22,000+ ELISA Kits, 26,000+ Antibodies, 15,000+ Proteins, 300+ Biochemicals Offered Services: Gene Synthesis, Peptide Synthesis, Protein Expression and Antibody Production Services To date, in addition to our catalog products, Biomatik has delivered 52,000+ custom-made products to our researchers worldwide. You can count on the quality products and tech support from Biomatik for your research needs. Please​ view our customer testimonials and some of the well-respected publications citing our fine products at Google Scholar​. Biomatik works closely with its partners at the R&D and production levels, along with 35+ distributors all over the world. Our goal is to provide worldwide researchers with high-quality research products and customized solutions at highly competitive prices - to be a truly valuable partner in unveiling the mysteries of the life sciences. We sincerely invite you to join our list of satisfied customers worldwide.

Expertise in both microbial fermentation and chemical synthesis allows us to tackle today's development pipeline's increasingly complex molecules. In fact, we thrive on the vexing challenges few CDMOs would have either the expertise or desire to address. Bold vision, along with the passion and commitment to make that vision reality, is at the heart of our organization. We are a forward-thinking, North American CDMO Pharmaceutical company specializing in clinical-to-commercial scale production capabilities for: Synthetic small molecules Fermented small molecules Highly potent APIs Biologics Bioreagents Flexibility, creativity, and dedication to process optimization are at the heart of our method and process development as well as quality and compliance efforts. We assure the programs advance on time and with the highest quality outcomes under our project managers' leadership.

Be Clinic Ready! Corealis Pharma provides services on a contract basis in the areas of Formulation & Process Development as well as in small scale Clinical Trial Material (Phase I and II) Manufacturing and the packaging of solid dosage forms (tablets & capsules) to pharmaceutical and biotech companies. Our services include: API characterization; salt selection; pre-formulation; formulation & process development; analytical method development; stability storage & testing; technical transfer and scale-up; cGMP manufacturing & packaging of Phase I and II CTM; dossier support for American, European, and Canadian submissions. Our experts have access to modern well equipped R&D and cGMP manufacturing & packaging facilities that allow them to successfully complete the most challenging and complex mandates. The primary objective of Corealis and its staff is to make every one of their customers succeed. Corealis Pharma Inc. offers personalized and efficient services in the areas of Formulation Development and Clinical Supply Manufacturing of solid oral dosage forms.

Custom Biologics is a regulatory compliant large molecule bioanalytical CRO specializing in the potency assessment and clinical testing of biologic-based drugs, vaccine, and gene therapy products. Our scientists and quality assurance team provides exceptional, high quality, customized assays to measure the functional properties of cellular and biotherapeutic drug candidates. We are a Health Canada audited, GMP-compliant, global service provider for functional testing of biotherapeutics, biosimilars and antibody drug conjugates. For nearly 20 years, our scientists have been designing and validating sophisticated bioanalytical assays to characterize and measure the therapeutic potential of large and small molecule biotherapeutics. Our work supports regulatory drug submission applications from biopharmaceutical companies throughout North America, Europe and Asia. Great Science - It's at the heart of everything we do!

Dalton is a contract pharmaceutical manufacturer which provides integrated chemistry, development, and manufacturing to biotechnology and pharmaceutical clients around the world. In its 42,000 sq. ft. facility, Dalton operates - cGMP manufacturing of Active Pharmaceutical Ingredients (APIs), - sterile injectables, - finished drug products in vials or syringes - solid oral dosage forms. APIs can be produced in gram to kilogram quantities, including sterile APIs. Dalton contract capabilities can support you at any stage of the regulatory process (Phase I, II, III, or commercial). Development services include - chemistry and process development, - medicinal chemistry, - custom drug conjugation, - targeted drug delivery systems, - analytical method development and validation, - ICH stability testing, - formulation, and - polymorphism screening. Dalton also supports the industry's pharmaceutical research programs with a catalog of 2,500 reference standards, building blocks, metabolites, and impurities with its Dalton Research Molecules division.

Everest Clinical Research ("Everest"​) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Operating primarily in North America, with headquarters located in Markham, Ontario, Canada, with additional offices in Little Falls (Greater New York City Area), New Jersey, USA, and Shanghai, China. Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us…that's Everest! Important Information for job candidates: Please be aware of cyber-security due to some fraudulent job scams. Everest will follow our standard and thorough recruitment process which will include video panel interviews: https://www.ecrscorp.com/recruitment-process/ Everest email communication will come from an ecrscorp.com email address. Emails from other domains may not be from Everest. Everest will never ask for credit card information or charge fees at any time during the recruitment process. If something is portrayed as Everest but does not appear to be from Everest, please feel free to contact us at https://www.ecrscorp.com/contact/

At Eyam, our mission is to bring “Next Generation” vaccine and therapeutic technologies to market to solve today's health care needs.

Immuni T is a CRO company, specialises in services for biotherapeutics and immunomodulators at very competitive rates. It has expertise in customized cell-based assays, flow cytometry and ELISA assays in bioanalysis in GLP/GCLP regulated laboratories. We have developed an ex vivo method for assessing the immunogenic potential of new biotherapeutics and biosimilars, an assay performed in freshly-collected PBMC from a number of donors. This assay, for example, could assist you in the selection of the less immunogenic lead from a set of variants or to compare the immunogenic profile of a biosimilar to that of its originator. It is a rapid and cost-effective means for the evaluation of the immunogenic potential of a molecule in a human system. We perform the development and validation of immunogenicity methods and of ligand-binding assays for PK analysis for pre-clinical and clinical programs. We developed functional customized cell-based assays such as cytotoxicity assays (e.g. ADCC, CDC, in PBMC, sub-cell compartments or whole blood) and other assays such as Treg or NK functional assays. Overall, Immuni T performs cell-based assays, human ex-vivo immunogenicity prediction/comparison assays for new biotherapeutics as well as immunogenicity tests for biotherapeutics in clinical development; ligand-binding assays for the quantification/detection of peptides, proteins or nucleic acids; immuno assays based on flow cytometry analysis for determination of cell function and molecules quantification; multiplex analysis on Luminex as well as customization, development and validation of assays for pre-clinical (in GLP-compliant environment) and clinical studies.

Innovotech is a pioneer in the field of biofilm product development, focused on providing innovative and practical solutions to medical, agricultural and industrial problems caused by microbial biofilms. Biofilms are organized communities of microorganisms that exist in virtually every natural environment and are responsible for a host of diseases in human health, animal health and agriculture. Innovotech has a broad range of products that address the issue of biofilms within a number of different industries, including commercially available products in three market segments; the MBEC Assay™, bioFILM PA™ and InnovoSCEPT veterinary kits. The MBEC Assay™ is a high throughput biofilm growth device that was recently approved as an ASTM International standard. bioFILM PA™ is the first diagnostic kit to assist physicians in the selection of the most effective combination antibiotic treatment of patients with biofilm-based chronic lung infections, while the InnovoSCEPT veterinary kits are designed to determine the most effective antibiotic treatment for infections in both large and small animals. Innovotech also has two products in advanced stages of development; Agress® is a unique, environmentally friendly seed treatment and plant spray designed to protect crops against both bacterial and fungal infections and Sani-Lux™ is a light-activated, natural hard surface sanitizer.

Transpharmation is a contract research organisation led by scientists. As the largest boutique Neuroscience-specialised small and large animal CRO, we can connect drug developers with world-leading technology platforms. Recognised by drug developers worldwide for researching and delivering life-changing medicines, science will always remain our passion. Our clients benefit from decades of experience in cross-species and cross-therapeutic area translational biology throughout our preclinical services. Success is measured by results and driven by a desire to make a difference. Our breadth of neuroscience expertise means clients are able to benchmark their compounds against clinical gold standards in well validated behavioural and molecular assays. Whether you are interested in pain models, sleep models or anything in between, please don't hesitate to contact us. We are committed to on-time data delivery and flexibility in deal structuring for your project. As such we will work alongside you in collaborative research, via contract work or in a full-time capacity, wherever you are around the globe. NEW! Transpharmation and InterVivo Solutions have united to form the largest boutique Neuroscience-specialised small and large animal CRO. Transpharmation's Facilities Management Company, Agenda Life Sciences, are one of only 14 establishments to hold the globally recognised AAALAC accreditation assuring clients of scientific validity and reliable, robust scientific outcomes.

ITR Canada provides preclinical testing services for the pharmaceutical and biotechnology industries. Since our founding in 1989 we have grown into a mid-sized Contract Research Organization (CRO). As a CRO with extensive experience, we provide you with valuable input and best practices, which ultimately help you maximize the value of your research investment. We deliver on time project reporting that meets your company's goals. ITR Canada offre des services d'essais précliniques pour les industries pharmaceutiques et de biotechnologie. Depuis notre création en 1989, nous nous sommes développée en une organisation de recherche contractuelle (CRO) de taille moyenne grandissante. En tant que CRO avec une vaste expérience, nous vous fournissons une contribution valable et les meilleures pratiques disponibles, qui vous aident finalement à optimiser la valeur de votre investissement en recherche. Nous vous livrons des rapports de projet en temps voulu et qui répondent aux objectifs de votre entreprise.

Since 1997, KGK Science has played a key role in the natural health product industry by providing our clients with high-quality clinical research and regulatory expertise to bring safe and effective products to global markets. As a full-service premium contract research organization (CRO) supporting the nutraceutical, cannabis and hemp industries, KGK is one of the most reliable resources for brands looking for an experienced, trustworthy team of scientific researchers, consultants, and regulatory specialists to develop customized claim substantiation and path-to-market strategies. From clinical study design to impactful product marketing, KGK has client success down to a science. At our state-of-the-art clinical research facilities, clinical staff, researchers, and regulatory experts quickly turn requests into results. We've guided hundreds of companies in taking their initial product concepts on to clinically proven claims and beyond, working to differentiate ideas and offer unique pathways through complex regulatory bodies including Health Canada, FDA, and FTC. Recognized globally as thought-leaders in cannabinoid science and regulation for the natural health product industry, KGK Science is proudly the first CRO in Canada to possess a Cannabis Research License, extending our 22 years of industry experience to include cannabis and hemp-derived products. As the leading CRO in the cannabis industry, KGK is focused on expertly conducting clinical trials and providing regulatory support to help bring innovative new health products to market, continuing to further global research and unlock the true value of the cannabis industry for clients and consumers.

Neurodyn utilizes a portfolio approach to identify, validate, and develop bioactives for neuroprotection and the early treatment of neurological diseases.

Norgen Biotek has been committed to customizing high-quality and innovative research tools to serve the scientific community for the past 25 years. Our mission is to provide the highest quality products and services to keep inspiring scientists to find new discoveries for the world. Subsequently, we focus on manufacturing sample collection, preservation, extraction, and detection products to enable our customers to achieve high throughput insights. We provide solutions to our customers in Life Sciences and Molecular Diagnostics. Furthermore, our products are distributed worldwide, and our technology has been featured thousands of times in peer-reviewed scientific publications by researchers from different institutions. Additionally, we have a team dedicated to providing Next Generation Sequencing Services with mastery in handling ultra-low concentration sample types, such as liquid biopsies and exosomes. At Norgen Biotek, we are #AlwaysReady to start long-lasting relationships and guarantee to meet customers' expectations. Working together, we can make the world better for all living beings. For more information, please visit norgebiotek.com.

Nutrasource is a full-service contract research organization (CRO) that helps health companies bring products to market with strong science and regulatory confidence - from concept to claim. Through our vertically-integrated service platform, Nutrasource is your one-stop shop for international regulatory, clinical, and product testing solutions for dietary supplements, pharmaceuticals, and everything in between. As your virtual R&D department, we will help you tackle your toughest scientific problems so you can sell safe, effective, high-quality products to improve healthcare globally. Originally established as a diagnostic test provider nearly two decades ago, Nutrasource has since grown from a single desk to a global CRO employing over 100 staff across four sites in North America. By focusing first and foremost on the needs of our customers, we are proud to have helped hundreds of clients develop, launch, and market health products across the globe.

Pharma Inventor Inc. is a Canadian Chemistry R&D and Analytical Services company established to serve the needs of pharmaceutical, biotech and agrochemical industries as well as research institutes/academic research groups in North America to support their innovative R&D/Analytical testing activities. Reach out to us for Custom Organic Synthesis / Medicinal Chemistry / Analytical Services / Process Chemistry Works / IP Consultation.

Pharma Medica Research is a full service early phase contract research organization. We offer an innovative approach to the design and implementation of clinical trials in support of pharmaceutical and biotechnology companies'​ drug development projects around the globe. * 360 bed phase I clinical capacity * Bioanalytical lab * Onsite organic synthesis lab * Biorepository services * Clinical data management * Medical writing * PK / Biostatistics * Clinical trial monitoring In addition to FIH, BA/BE, and PK/DDI studies, we have specialized skills in respiratory, transdermal delivery systems (including SIS studies), and patient PK studies. Our reputation is built upon principles of on-time performance, responsiveness to the industry we serve, and delivery of uncompromising quality at reasonable costs. Our client-focused approach truly differentiates us from other contract research organizations. Pharma Medica Research has developed processes that put the needs of our clients first. These include flexible study scheduling, rapid preliminary results turnaround and prompt final report delivery. Outsourcing should not be complicated. We are there to make your project implementation as simple as possible.

StarFish Medical provides award-winning design, development, and flexible manufacturing outsourcing services —100% dedicated to the medical device and life science marketplace. StarFish partners with innovative companies to create and manufacture breakthrough products for a full range of medical specialty areas including: Cardiovascular, Digital Health, IVD, Ophthalmology, Optics, Ultrasound, POC Assay Diagnostic Technologies, and Microfluidics. StarFish expertise includes electronics, mechanical, human factors and software systems engineering. Our proprietary Pathfinder™ process for medical device product definition saves clients time and resources throughout the technology and product development phases to commercialization. Prototype and low volume complex electro-mechanical production are delivered in ISO 13485 certified facilities with cleanroom capabilities in Toronto and Victoria Regulatory and quality system (QMS) consultants at StarFish provide technical regulatory assistance for FDA and Health Canada submissions, including IEC 60601 and ISO13485. Innovative Design and Development  Electronic / software / mechanical engineering  Industrial design / human factors engineering  PathfinderTM product definition process  Technology optimization  Verification / validation / testing  ISO 13485 certified QMS Integrated Manufacturing  Seamless ramp from clinical trials to full production  Deep engineering involvement & oversight  Electro-mechanical / software expertise  Customized cart specialists  Optical instrument build and test  Dedicated program manager Flexible Manufacturing  New product introductions  Supply-chain management  North America facilities  Depot repair & field service  Sustaining / value engineering  Class 100,000 cleanroom

Valence Labs is a biotechnology company that specializes in AI-driven drug discovery. It operates as a semi-autonomous research and productization engine within Recursion Pharmaceuticals. The company focuses on leveraging deep learning applications to enhance drug development, particularly for complex diseases. Valence Labs develops software tools that accelerate therapeutic research, including novel target identification and molecular design. In addition to its AI-driven initiatives, Valence Labs is associated with a separate entity that specializes in active pharmaceutical ingredient (API) synthesis. This division offers custom API manufacturing services, including process development and GMP-compliant commercial-scale production. Valence Labs collaborates with biotech partners to provide AI solutions, emphasizing complex chemistry and preclinical optimization.

Veristat is a Massachusetts-based CRO that provides services such as regulatory consulting, medical writing, and monitoring for the pharmaceutical industry.