Clinical Trials Phase I to IV

Clinical Trials Phase I to IV Companies (33)

Clinical Trials Phase I to IV News

Clinical Trials Phase I to IV Products (41)

  • Product Clinical API Development

    CARBOGEN AMCIS has a DNA in API development, stretching back over 30 years. Our API development teams are selected for their passion for science and experience in the application of phase-appropriate efforts to solve challenging chemistry issues. From taking a promising molecule from our clients' medicinal...
  • Product Clinical Research Solutions

    We design and execute clinical trials so new therapies get to market in the quickest and safest way possible. Full-Service Solution: We manage and execute full-service clinical trials across major therapeutic areas within medical device, diagnostics, drug, and biologic. Functional Service Provisi...
  • Product Bioanalytical Services (GLP/GCP)

    Services for Bioanalysis (GLP/GCP): In our state-of-the-art facilities, we provide GLP/GCP method development, validation, method transfer, sample analysis and pharmacokinetic and toxicokinetic support, along with automated data collection and reporting systems. Over the past 20 years, we have supported...
  • Product Small Molecule - Phase 3 or Commercial Support

    Taking the molecule to market• Fate & purge studies
    • Impurities marker synthesis &qualification
    • Design of experiments
    • Critical process parameters studies
    • Preparation for, and execution ofprocess validation
    • Continuing CMC support during &after market launch
    • Technolog...
  • Product Clinical batch production

    XEDEV can support clinical batch manufacturing up to Phase IIb in our clean rooms after succesfull development.

  • Product CRO services - Clinical trials with probiotics and other food supplements

    Bioithas' main activity since its inception has been carrying out clinical studies in humans, both its own clinical trials and services to other companies in the pharmaceutical, biotechnology and nutritional industries.

    At Bioithas, we carry out all stages of the clinical project, from trial des...
  • Product Clinical Manufacturing

    .Integrated drug development service (CRO/CDMO) including clinical manufacturing and management.
    The range of activities offered by Bluepharma includes:
    - Clinical material cGMP manufacturing
    - Clinical supply management
    - clinical material
    - placebo
    - ...
  • Product Passionis

    Passionis is a unique product specially for women, which have been related to sexual appetite boost properties, containing Liboost, Maca, Vitamin B6 and Zinc.
  • Product Clinical Manufacturing

    KBI Biopharma offers a broad range of cGMP biologics manufacturing services to biopharmaceutical companies worldwide. Our capabilities include reliable manufacturing for preclinical and clinical supply.

    KBI’s experienced team produces high-quality therapeutics and vaccines thro...
  • Product Clinical Supply

    Recipharm have more than 20 years experience supplying clinical trial material to our clients. Our development facilities cater for a range of clinical trials from preclincal to smaller Phase III trials. We also offer commercial manufacturing for very large clinical batches.
  • Product GALENIC DEVELOPMENT

    TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing

    GALENIC DEVELOPMENT
    • Preformulation studies.
    • Design and galenic develop...
  • Product Clinical Pharmacology

    When you are looking for a partner who is dedicated to Phase I trials and early clinical development, rely on Quotient Sciences for the experience and expertise to seamlessly deliver your studies with the highest quality service and speed. We accelerate your molecule from first-in-human to proof-of-concept...
  • Product Antibody Drug Conjugates (ADC)

    hen selecting AbbVie Contract Manufacturing, you are partnering with a leading developer and manufacturer focused on accelerating and mitigating risks to program timelines and on efficiently fast-tracking your program to completion. AbbVie’s mAb and ADC state-of-the-art facility and expert scientific team ...
  • Product Biologic drug substance CDMO services

    From pre-clinical development to commercial supply, Patheon by Thermo Fisher Scientific is an industry leader in the development and manufacture of mammalian cell culture drug substances. Patheon offers biotech and pharmaceutical companies the ability to pursue opportunities around the globe with a fully i...
  • Product Drug Product Development

    Our Vetter Development Services help biopharma customers lay a foundation of scalability, quality, and sustainable value for drug product profiles. We support drug developers in navigating key steps, decisions, and transitions in the product development cycle. This includes primary packaging evaluation, pr...
  • Product Life Science Logistics

    Life Couriers provide trusted Life Science logistics support on a global scale.

    Our solutions provide dependable transportation for CROs, hospitals, labs, universities and research organizations around their world, the backbone for their vital work in clinical trials, cell and gene therapy, and ...
  • Product Comparator Drugs / Reference Samples / Formulation & Whitelableing

    NewLife Medicals is the preferred partner in strengthening supply chain for Innovation and R&D in Pharmaceuticals. As a dedicated pharma raw material supplier, we play a pivotal role in providing essential components for the advancement of pharmaceutical research. It is actively engaged in sourcing Ref...
  • Product Early Phase Clinical Study Expertise

    State-of-the-art phase I/ll unit supporting complex clinical trials • First in Human ( FIH) to Proof of Concept ( PoC) • Clinical pharmacology studies through all phases • In-house safety lab and bioanalytical services • Special patient populations (with a focus on respiratory) • Data m...
  • Product Bioequivalence studies

    Intertek offers wide range of pharmaceutical services which includes bioequivalence studies. It belongs to bioanalytical services for preclinical and clinical studies category. Contact us for more information.
  • Product EU/UK Qualified Person (QP) Services and MIA license

    Navigating both general and country-specific regulations and requirements to supply medicinal products to the European markets can be a complex challenge for Marketing Authorization Holders (MAH). ProPharma holds both EU and UK MIA licenses which allows us to help clients overcome the complexities of su...

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Recommended Products And News

  • Product Biologic drug substance CDMO services

    From pre-clinical development to commercial supply, Patheon by Thermo Fisher Scientific is an industry leader in the development and manufacture of mammalian cell culture drug substances. Patheon offers biotech and pharmaceutical companies the ability to pursue opportunities around the globe with a fully i...
  • Product Outsourcing

    Patheon by Thermo Fisher Scientific has a broad manufacturing platform for pharmaceutical and biologic products which provides sustainable solutions for mammalian cell-based and microbial-based manufacturing, green chemistry R&D and manufacturing technologies, and finished dosage production of biopharm...
  • Product Clinical Pharmacology

    When you are looking for a partner who is dedicated to Phase I trials and early clinical development, rely on Quotient Sciences for the experience and expertise to seamlessly deliver your studies with the highest quality service and speed. We accelerate your molecule from first-in-human to proof-of-concept...
  • Product Clinical API Development

    CARBOGEN AMCIS has a DNA in API development, stretching back over 30 years. Our API development teams are selected for their passion for science and experience in the application of phase-appropriate efforts to solve challenging chemistry issues. From taking a promising molecule from our clients' medicinal...
  • Product Clinical Trial Services

    Our experts will accomplish your clinical objectives by leading the way from recruitment strategies, site selection, and clinical logistics, all the way through the regulatory process. 

    We use our own eClinical suite to be more cost-efficient and keep you connected remotely acros...
  • Product PharmaLex

    PharmaLex is one of the largest providers of Development Consulting, Regulatory Affairs, Quality Management & Compliance and Pharmacovigilance worldwide. Our global teams of experts can take you through early strategic planning activities and nonclinical requirements to clinical deve...
  • Product Clinical Manufacturing

    KBI Biopharma offers a broad range of cGMP biologics manufacturing services to biopharmaceutical companies worldwide. Our capabilities include reliable manufacturing for preclinical and clinical supply.

    KBI’s experienced team produces high-quality therapeutics and vaccines thro...
  • Product BDD Scintigraphy

    Gamma scintigraphy is a powerful and versatile technology used to investigate the in-vivo performance of your drug or product. This non-invasive imaging technique allows us to follow the fate of the dosage form and administering it to a volunteer or patient. Not limited to just oral dosage forms, gamma sci...
  • Product ResearchMods-accellerate your clinical trial

    ResearchMods by M3E Solutions is a digital solution which accelerates clinical trials in hospitals through workflow optimzation, knowledge transfer and information chunking. Patient inclusion increases by up to 16%, error rates are reduced by up to 29% and workload reduces by up to 32%.
    Intelligent op...
  • Product TIM-2

    The TIM-2, as part of the SurroGUT™ platform, is the dynamic in vitro model of the large intestine. The lower GI model, with its anaerobic compartment containing highly metabolic active intestinal microbiota, precisely mimics the physiological conditions of the colon in vivo. TIM-2 can simulate the pr...
  • Product Clinical solutions: Trials

    Conscio's in-house clinical Unit has been operating since 2007, with more than 600 BA/BE/PK studies completed and proprietary of over 270 validated bioanalytical methods. Equipped with a 60-bed on-site clinical unit in Prague and a recently opened 36-bed unit in Ostrava, we provide comprehensive services w...
  • Product Certified toxicological studies

    Toxicological tests performed at the Lukasiewicz - IPO:
    -allow a toxicological evaluation of chemical substances contained in pharmaceutical products, veterinary medicinal products, plant protection products, food and feed additives, industrial chemical substances, etc.,

    -make it possi...
  • Product Cortellis Regulatory Intelligence™

    Navigate the regulatory landscape and efficiently drive strategic decisions with Cortellis Regulatory Intelligence. Get full and timely coverage of global health authority requirements on healthcare products such as drugs, biologics, medical devices and IVDs, and access exclusive expert reports for both in...
  • Product CDMO Biopharmaceutical Production

    With an extensive offering of development services, state-of-the-art manufacturing equipment, and project support, GBI is truly a full-service CDMO biologics partner. Our approach pairs our expert knowledge base with an open mind towards scientific discovery so that together we can develop an optimal way t...
  • Product Cell-based Neutralization Assays

    Experienced cell-based neutralizing antibody assay capabilities. Our experts, at our GLP/GCP compliant laboratory, evaluate each therapeutic, conduct tailored assay development and ensure that each assay is optimized to suitably determine the presence of NAb with maximum possible level of drug toleran...
  • Product GENETIC DIAGNOSIS - Pharmacogenetics

    TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing

    TECNALIA´s Genetic and Molecular Biology  Lab develops a strong activity in the field of Genetic Diagnosis, focused on three main areas:
    • Diagnosis...
  • Product CRO Services

    Clinical Development Program (Phase I to IV) Product Registration 
    Pharmacovigilance
    Regulatory Affairs
    Clinical Monitoring 
    Medical Monitoring
    Project Management 
    Medical Writing 
    Quality Assurance - GCP Audits 
    Logistics Coordination 
     
  • Product Clinical Supply Manufacturing

    NCEs • Phase I-III formulation process development and clinical supply manufacturing Generic drugs
    • BE sample manufacturing • Process Optimization
  • Product Drug Product Development

    We support our clients from early-stage research and preclinical phase to and beyond market approval by providing comprehensive development services, including 

    • Developability assessment • Pre-formulation screening • Formulation development • Lyophilization process development • Forced d...
  • Product Small Molecule - Phase 3 or Commercial Support

    Taking the molecule to market• Fate & purge studies
    • Impurities marker synthesis &qualification
    • Design of experiments
    • Critical process parameters studies
    • Preparation for, and execution ofprocess validation
    • Continuing CMC support during &after market launch
    • Technolog...
  • Product Clinical Research Solutions

    We design and execute clinical trials so new therapies get to market in the quickest and safest way possible. Full-Service Solution: We manage and execute full-service clinical trials across major therapeutic areas within medical device, diagnostics, drug, and biologic. Functional Service Provisi...
  • Product Antibody Drug Conjugates (ADC)

    hen selecting AbbVie Contract Manufacturing, you are partnering with a leading developer and manufacturer focused on accelerating and mitigating risks to program timelines and on efficiently fast-tracking your program to completion. AbbVie’s mAb and ADC state-of-the-art facility and expert scientific team ...
  • Product UNITYai.Lit

    Elevate your literature management with Unityai.Lit - the advanced software platform and the ultimate solution for efficient and validated ICSR processing and identification of publications for signaling and aggregate reports. Developed by Soterius, Inc., Unityai.Lit is not just a tool; it's a transformati...
  • Product PILOT BATCHES AND REGISTRATION BATCHES CONTRACT MANUFACTURING

    TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract ManufacturingPilot

    Batches and Registration Batches /
    • Manufacture in compliance with the principles and guidelines of GMP for medicinal products.
    • Transfer o...
  • Product BDD Swift - adaptive clinical studies

    •SWIFT accelerates evaluation and optimisation of product performance using in vivo clinical data to direct formulation design in real time.
    •SWIFT studies enable you to make decisions on formulation changes based on emerging clinical data. • This integration of formulation development, GMP manufactu...
  • Product Preclinical Functional Neuroimaging

    neuroPhINDr is our answer to the problem of low translational value of preclinical neuroimaging. With neuroPhINDr, we aim to shorten time-to-market, increase confidence in preclinical results and improve success rates in phase I trials. neuroPhINDr is a set of highly optimised and standardised protocols fo...
  • Product Clinical Research Services

    At ProRelix Research, our dedicated clinical trial project management team provides Phase 1, 2, 3, and 4 clinical research services in compliance with the principles of ICH & GCP, trustworthy clinical safety services, site selection based on their history of meeting enrollment targets, and consistent d...
  • Product Pre-Clinical Services

    Our 3 platforms available are: • Solubility • Solid Dispersion • Nanoparticles
  • Product Clinical Trial Reporting

    The Atlantia Clinical Research team provides a comprehensive study reporting service. Our statisticians adhere to ICH-GCP standards to produce a statistical study report, and if the client requests, a full clinical study report.Atlantia maintains no rights to Intellectual Property generated from this study...
  • Product R&D Services

    Our R&D Services are categorized into 8 streams: • Material Science Services

    • Metal and Organic Scavenging Screening Services

    • Organic Synthesis Services

    • Catalysis Services

    • Process Services

    • Chromatography and Purification Services

    • Method D...
  • Product Netpharmalab Consulting Services

    Contract Research Laboratory. Analytical Services (physicochemical analysis, microbiological analysis and stability studies) and EU Import Lab.
  • Product EU/UK Qualified Person (QP) Services and MIA license

    Navigating both general and country-specific regulations and requirements to supply medicinal products to the European markets can be a complex challenge for Marketing Authorization Holders (MAH). ProPharma holds both EU and UK MIA licenses which allows us to help clients overcome the complexities of su...
  • Product Translational Pharmaceutics - Integrated Programs

    Translational Pharmaceutics® accelerates drug development by integrating formulation development, real-time manufacturing and clinical testing. The platform is unique to Quotient Sciences and has been used over the last decade by global pharmaceutical and biotech companies across over 400 drug programs. qq...
  • Product tiny-TIMsg

    The tiny-TIMsg system, as part of the SurroGUT™ platform, precisely mimics the upper GI tract and all physiologically relevant processes; including the pressure, shear forces and phase specific gastric emptying. The tiny-TIMsg consists of an advanced gastric compartment (TIMagc) and small intestine co...
  • Product Drug Product Development

    Our Vetter Development Services help biopharma customers lay a foundation of scalability, quality, and sustainable value for drug product profiles. We support drug developers in navigating key steps, decisions, and transitions in the product development cycle. This includes primary packaging evaluation, pr...
  • Product Data Sciences

    You need data rapidly to make crucial decisions during a study. Faster data means we can provide our customers with earlier interim data and interim PK reports for on-study dosing and formulation decisions.
    We understand on-study changes to early phase study designs and d...
  • Product Small Molecule - Early Phase to Phase 2 Support

    Setting the stage for the commercial process:• Route or step rebuild
    • Process optimization &demonstration
    • Impurities assessment & synthesis
    • Full structure characterization &elucidation
    • Analytical method development &qualification
    • Stress studies & ICH st...
  • Product eClinical suite

    The Clinvigilant eClinical suite includes: EDC, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them with your existing software ecosystem.

    Clinvigilant is a global cost-effective eClinical tools provider for Pharma, Biot...
  • Product Custom Protein Synthesis

    We provide a Custom Protein Synthesis Service, using a chemical method that synthesises proteins amino acid by amino acid and making modifications on an atomic-scale. We work closely with our partners in designing, customising and optimising the proteins that is synthesized in an automa...
  • Product Cortellis Clinical Trials Intelligence™

    Confidently and efficiently plan and design clinical trials by reducing time spent compiling and analyzing protocols, sites, outcomes, endpoints and more. Avoid costly protocol amendments, recruitment delays and trial failure by tracking competitive trials, selecting experienced sites, defining the right e...