Analytical Development & QC

Analytical Development & QC
Product Description

Based on an analytical continuum our testing experts provide solutions all along the value chain from early discovery to clinical trials including method development, validation, quality control, stability studies of the main physicochemical and microbiological testing for innovative and generic products.

Nuvisan GmbH

  • DE
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Contract Service

Nuvisan GmbH

  • DE
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Contract Service

More Products from Nuvisan GmbH (18)

  • Quality Management

    Product Quality Management

    Nuvisan GmbH provides wide range of pharmaceutical services which includes quality management. It provides and maintains a comprehensive quality management system to allow each department to manage their project based on processes that have been documented and validated by operations and management. Based ...
  • Regulatory Affairs

    Product Regulatory Affairs

    Nuvisan GmbH provides wide range of pharmaceutical services which includes regulatory affairs. Benefits: extensive experience with pharmaceutical start-ups, from contract research organisations to large pharmaceutical companies experienced with a wide range of product types including chemical drug substanc...
  • Training

    Product Training

    Nuvisan GmbH provides wide range of pharmaceutical services which includes training. Pharmaceutical expert with more than 18 years of comprehensive experience (cro and sponsor side) in the field of clinical research (clinical operations, training, coaching, mentoring, quality control, quality assurance) an...
  • Early Phase Clinical Study Expertise

    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...
  • Manufacturing, packaging & distribution service

    Product Manufacturing, packaging & distribution service

    With more than 40 years’ experience as a Clinical Trial Supplies service provider, NUVISAN offers the full range of services in the area of clinical drug supply including: • Regulatory consultancy, CMC support • Non-sterile manufacturing services, including matching placebos • Packaging and lab...
  • Chemical Development

    Product Chemical Development

    For the pharmaceutical, veterinary or cosmetic industry, our chemists have experience in route scouting and in developing scalable, innovative, sustainable, safe and robust processes up to GMP manufacturing for toxicological and clinical studies. We are also experienced at handling and manufacturing from t...
  • Clinical Trial Supply

    Product Clinical Trial Supply

    NUVISAN has over 40 years of experience providing clinical trial supplies services, offering a comprehensive range of solutions. These solutions include regulatory consultancy, manufacturing services, packaging and labeling, randomization list creation, analytical testing, just-in-time labeling and distrib...
  • Formulation Development

    Product Formulation Development

    The NUVISAN formulation group up has a proven heritage of effective product development with team members being responsible for the creation of topical formulas that supported several commercially successful products. These successes were underpinned by our focus on innovation and patient and health care p...
  • Bioanalytical Services

    Product Bioanalytical Services

    To effectively support your drug development project and maximize your R&D productivity, NUVISAN offers a wide array of bioanalytical solutions for small and large molecules. Starting at the discovery, all the way through phase IV, we offer expertise bioassays and high-sensitivity ligand-binding assays...
  • Formulation Development

    Product Formulation Development

    Nuvisan GmbH provides wide range of pharmaceutical services which includes formulation development. Service portfolio: formulation development / clinical manufacture; capsules; tablets; granulation / pellets; coating; opcs - powder in the bottle; impd generation: > 55 filings; clinical packaging; phase 1 c...
  • Immunology

    Product Immunology

    Nuvisan GmbH provides wide range of pharmaceutical services which includes immunology. The testing according to ema guidelines: assay development, validation and glp-compliant performance; screening assays; confirmatory assays assays for neutralizing antibodies; various elisa formats available: bridging, d...
  • Medical Affairs

    Product Medical Affairs

    Nuvisan GmbH provides wide range of pharmaceutical services which includes medical affairs. Study success is best achieved by a combination of operational excellence, technology and medical oversight. A team of medics, biostatisticians, pharmacovigilance staff and additional experts can cover the full rang...

Nuvisan GmbH resources (6)

  • Brochure Chemical Development Solution

    NUVISAN`s scientific team has extensive knowledge in the development of chemical processes up to GMP manufacturing for pre-clinical and clinical studies. We specialize in developing and manufacturing active pharmaceutical ingredients (APIs) and intermediates, offering support from early-stage R&D to commercialization.
  • Video Integrated Therapeutic Solutions: Dermatology

    At NUVISAN, our passion is creating safe and effective topical products to improve the lives of millions of patients worldwide. Our team of experts is dedicated to drug discovery, DMPK, chemical and formulation development, manufacturing, and clinical development. We create innovative, stable, and elegant topical formulas that have high potential for clinical and market success. With locations in Germany and France, as well as a network of depots worldwide, NUVISAN ensures efficient logistics and support for clinical trial sites globally.
  • Brochure ALS‘s Strategic Acquisition Drives Innovation and Science

    With ALS's extensive portfolio spanning from drug discovery to post-commercialization, this strategic acquisition offers specific opportunities for our clients
  • Brochure Analytical Development and QC Solutions

    our testing experts provide solutions all along the value chain from early discovery to post-commercialization.
  • Brochure Clinical Trial Supply Solutions

    With more than 40 years of experience, NUVISAN provides a comprehensive range of solutions in clinical drug supply including regulatory consultancy, packaging..
  • Brochure Dermatology And Topical Development Solutions

    The NUVISAN formulation group has a strong track record of developing effective topical formulas that have supported numerous commercially successful products.

Frequently Viewed Together

  • Product ADAPTEK® TECHNOLOGY

    ADAPTEK® TECHNOLOGY is the general name for our 4 international patents and expertise in nanotechnology and controlled release systems.This is a transversal technology that allows to develop customized biopolymeric nanohydrogels, allowing the load with different API (drugs, vitamins, growth factors, etc.)....
  • Product Pulmonary Delivery

    Where particle size and performance really matters, Upperton have the expertise.
    Drug delivery into the lung is one of the fastest growing, yet technically challenging areas of pharmaceutical development. Producing a successful pulmonary drug product requires expertise in formulation development, part...
  • Product Nitrosamine Analysis

    In response to nitrosamines present in pharmaceutical products, the European Medical Agency (EMA) and the US Food and Drug Administration (US FDA) have published requirements and limits related to nitrosamine contaminants. Therefore Brightlabs has developed and validated multiple methods to determine low l...
  • Product Development

    Synerlab provides wide range of services which includes development. Contact us for more information.
  • Product CMO/CDMO Services

    - State of the Art GMP approved Biotech and Sterile Drug Product Facilities

    - Pilot Scale Facility and Scale Up/Scale Down Model- QC Laboratory Capability and Lab Services- Available Capacity and customized CDMO/Solutions

    - On-Site Facilities Available for start-up Biotech/Pharma co...
  • Product Clinical Trial Material Manufacturing

    PMI Bio provides product development services and cGMP manufacturing for Phase I and Phase II clinical trials. Key capabilities include process development, non-sterile manufacturing and filling of liquids and creams, aseptic filling and finishing and the ability to provide microfluidization of liquids an...
  • Product Biotherapeutics

    To accelerate the development and marketing of your Biotherapeutics, Quality Assistance offers a complete analytical package to meet the EMA and FDA requirements, all on one site.

    Whether it is to extend your analytical capacities or to outsource parts or all of your analytical needs, ...
  • Product Analytical Services

    With a team of experienced scientists and a robust toolbox of analytical techniques and equipment, Experic can support the life cycle of your oral solid dose and/or inhalation pharmaceutical products. Our laboratory staff provides comprehensive analytical solutions to support the formulation, development, ...
  • 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 STABILITY STUDIES

    TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing
    We offer Stability Studies in short and long term,
    according to ICH standards.

    • Batchs of Registration.
    • Industrial batches of finished ...
  • Product Analytical Services & EU Batch Certification

    Method Development and validation
    Stability Studies
    European testing & batch certification

  • Product Analytical Development

    Recipharm offer analytical support for drug discovery, pharmaceutical development and manufacturing through our global development facilities.
  • Product Analytical Development

    With top expertise in protein analytics, KBI has successfully completed over 3300 analytical projects for more than 300 customers and more than 130 distinct molecules.


    Our experience includes antibodies (IgG1, IgG4, IgM, FAb, ADC, Fc fusion), enzymes, cytokines, growth factors, highly glycosylat...
  • Product Technical Project Management

    “You have an early development candidate – we take the responsibility to develop it and get it on the market”

    We use an integrated fast-track drug development approach to achieve this goal.

    • Sourcing • Chemical Development / Biotechnological Development • Pharmaceutical Develo...
  • Product Formulation and Analytical Solutions

    GVK BIO offers a range of Formulation R&D solutions that include pre-formulation studies, formulation development, analytical R&D, reformulation and stability studies. We can also support clinical supplies and manufacturing of exhibit batches in collaboration with our partners and offer standalone ...
  • Product Biosafety Testing & Analytical Development Services

    Choosing the right partner for analytical and biosafety testing is critical in the race to approval. Our BioReliance® Contract Testing Services offer exceptional, risk-mitigating solutions with technical and regulatory expertise, to help bring life-changing drugs to market.
  • Product Process Development:

    •Evaluating multiple synthetic pathways to determine the most efficient, cost-effective, and scalable route. 

    •Assessing raw material availability and sustainability to ensure a reliable and cost-efficient supply chain. 


     •Developing innovative strategies to minimize h...
  • Product A CDMO PARTNER FOR LIFE

    FUJIFILM Diosynth Biotechnologies is an industry-leading cGMP Contract Development and Manufacturing Organization (CDMO) supporting the biopharmaceutical industry in the development and production of biologics, vaccines and cell and gene therapies. Our focus is to combine technical leadership in process d...
  • Product GMP and CMC Laboratory Services

    Laboratory services according to GMP and CMC: We provide regulatory-driven, phase-appropriate laboratory services, supporting CMC programs from preformulation to formulation to product release. Among our capabilities are centres of excellence for method development and validation, analysis, stability s...
  • Product Pharmaceutical Reference Standards

    All Pharmaceutical Reference Standards are supplied with Certified COA along with supporting analytical data like HPLC, Mass, NMR, CMR, UV, IR, TGA, ROI, CHNS.
  • Product Analytical Services

    Pharmaffiliates is providing all the Analytical Services (i.e. Method Development, Method Validation & Transfer, Stability Studies, Contract Analysis, etc)
  • Product KinetiSol Technology

    The KinetiSol Technology generates amorphous solid dispersions, dramatically improving the bioavailability of poorly soluble drugs. KinetiSol is a fusion-based, solvent-free process that utilizes frictional and shear energies, in a fraction of the time of other ASD technologies. With its significantly smal...
  • Product GMP Analytical Testing

    Singota solutions offers wide range of services which includes GMP analytical testing.
    Studies & Methodologies: • Material Identity • In Process • Product Release • Product Specific Assays • Compendial • Microbial (Endotoxin, Bioburden, Sterility) • CoA Generation • ICH Stability (All ICH...
  • Product ATMP Analytical Development Services

    Advanced therapy medicinal product (ATMP) analytical services & chemistry, manufacturing, and control (CMC) support including characterisation, stability and release testing. Our GLP / GCP / GMP laboratories have supported developers and manufacturers for over 20 years through the provision of adv...
  • Product Drug Development

    Service Overview Drug Development and Manufacturing • Development of solid, semi-solid and liquid formulations for oral, topical, nasal and parenteral application
    • API characterisation and quality screening • Small batch manufacturing §Clinical trial batch manufacturing and distributio...
  • Product Quality Control Testing Services

    QC testing of pharmaceutical raw materials to international pharmacopoeia specifications has become a specialty of Intertek. With our knowledge of analytical chemistry and our vast range of instrumental techniques, we can undertake the vast majority of the chemical tests listed within the international pha...
  • 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 ANALYTICAL DEVELOPMENT

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

    Manufacturing ANALYTICAL DEVELOPMENT
    • Monitoring of the first industrial manufacturing batches.
    • Characterization of raw materials according to Pharmacopoeia. q...
  • 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 Chemical Development

    For the pharmaceutical, veterinary or cosmetic industry, our chemists have experience in route scouting and in developing scalable, innovative, sustainable, safe and robust processes up to GMP manufacturing for toxicological and clinical studies. We are also experienced at handling and manufacturing from t...
  • Product ICH Stability Testing, Storage & Program Management

    Our extensive capabilities cover all ICH conditions (or custom conditions), including climate control walk-in chambers, cabinets, refrigerated and freezer storage that are fully monitored and controlled, with backup units at every location. We have 24-hour alarm systems at all sites with dedicated teams on...
  • Product PHARMACEUTICAL ANALYSIS DEPARTMENT

    Spark-Lab Pharmaceutical Analysis Department performs routine analyses with a special emphasis on determination of excipients, such as:

    • Quantitative determination of sorbitol, glycerol, maltitol, mannitol in liquid forms based on our own method; • Quantitative determination of glucos...
  • Product Elemental Impurities

    Brightlabs has in-house validated methods for the analysis of elemental impurities in accordance to ICH-Q3D. Brightlabs has a unique approach for ICHQ3D, which guarantees quick turnaround times at reduced cost
  • Product Inhalation Drug Product Development Services

    Services for the development of inhalation drugs: Our team have over 30 years of experience supporting our clients' product development for orally inhaled or nasal drug products (OINDP). This includes formulation, stability, testing, product performance testing, in vitro bioequivalence studies, CMC...
  • Product Inhalation Test Services

    We are the world’s leading provider of orally inhaled and nasal drug product design and development services. We enable the seamless translation of pre-clinical development through to clinical manufacture of OINDPs. We do this through our unique processing technologies and formulation development tools....
  • Product Analytical method development

    MJR PharmJet uses its long gained experience on nano and microparticle formulations to meet your method development needs. We are specialized on the method development of particulate formulations for solid, semi solid and liquid formulations.
  • Product Analytical Development and expertise

    Our analytical experienced team support the pharmaceutical development during every phase of the development process. Analytical development transfer and validation, characterization capabilities, stability analysis, ICH Q3D (residuals solvent risk assesment), ICHQ3C (elemental impurities risk assesment...
  • Product Solid-State Characterization

    At Particle Analytical, our solid-state characterization services offer comprehensive analysis of polymorphism, crystallinity, and amorphous content, ensuring that every compound meets the highest standards of quality and performance. Utilizing advanced techniques such as X-ray powder diffraction ...
  • Product Analytical chemistry&Physico-chemical properties

    Determination of physical, chemical and technical properties of substances and chemical products

  • Product Kemwell Biopharma

    SERVICES Kemwell provides integrated development and manufacturing services for companies that require one-stop solution for mammalian cell-culture based protein therapeutics The team is experienced to undertake end-to-end activities right from cell line development till cGMP clinical and commercial manufa...
  • Product Analytical Development

    BioDuro-Sundia’s Analytical Testing team offers high quality analytical services including method development and validation, qualification of reference standards, testing and release studies, stability studies, and CMC dossier preparation services. ...
  • Product Analytical services - OEL: 50 ng/m3

    • Control of pharma samples solid state : Identification and quantification of solid state, method development and validation, routine QC. • Analytical techniques available : XRPD, DSC, TGA, DVS, Laser PSD, FTIR, IDR. • All analyses are applicable to toxic samples down to : 50 n...
  • Product Analytical Services

    Solvias provides cGMP-compliant contract analytical services to help you ultimately provide safer products to consumers. We provide a comprehensive range of analytical services to the pharmaceutical, biotech, medical devices and cosmetics industry with similar regulatory requirements for raw materia...
  • Product X-ray powder diffraction (GLP & GMP) for pharmaceuticals

    Intertek offers wide range of pharmaceutical services which includes x-ray powder diffraction (glp & gmp) for pharmaceuticals. It belongs to pharmaceutical analysis services category. It includes gmp services, stability and pharmaceutical testing, physical characterization techniques for pharmaceutical...
  • Product Method Development

    We are specialist in the method development of analytical methods for analysis of API, Final Drug Products or low level impurities. Usually followed by full validation in accordance to ICH guidelines.
  • Product Drug Stability Testing and ICH Storage Outsourcing

    Testing of pharmaceutical stability and ICH storage outsourcing: Our extensive capabilities cover all ICH conditions (or custom conditions), including climate control walk-in chambers, cabinets, refrigerated and freezer storage that are fully monitored and controlled, with backup units at every locatio...
  • Product Herbal Drugs Analysis

    Since 2018 Brightlabs possesses an opium exemption from the BMC (Bureau for Medicinal Cannabis), for the analysis of cannabis and related products. The combination of this opium exemption, combined with our GMP accreditation, makes Brightlabs an important partner for the analysis of cannabis and related ma...
  • Product R&D Research and Development

    The Pharmaceutical Analyses Department of Spark-Lab conducts research and development work in cooperation with pharmaceutical and cosmetics manufacturing plants. The Laboratory provides services through its highly skilled personnel and state-of-the-art equipment at the initial phase of works on a g...
  • Product Nebulised Drug Development Services

    Intertek Melbourn have been supporting clients’ product development for nearly 30 years across all classes of inhaled and nasal delivery technologies including nebulized therapeutics. We provide expert OINDP formulation development, product performance testing and analysis, in vitro bioequivalence studies,...
  • Product Clinical Trial Supply

    NUVISAN has over 40 years of experience providing clinical trial supplies services, offering a comprehensive range of solutions. These solutions include regulatory consultancy, manufacturing services, packaging and labeling, randomization list creation, analytical testing, just-in-time labeling and distrib...