Analytical Development & QC
Product Description
Nuvisan GmbH
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Country/Region:Germany
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On CPHI since:2015
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Certificates:2
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Employees:1000 - 4999
Company types
Categories
Nuvisan GmbH
-
Country/Region:Germany
-
On CPHI since:2015
-
Certificates:2
-
Employees:1000 - 4999
Company types
More Products from Nuvisan GmbH (4)
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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... -
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 management, regulatory sup... -
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 labelling services... -
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...
Nuvisan GmbH resources (3)
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Brochure CMC- Clinical trial supplies slutions
Nuvisan experts ensure smooth clinical drug supply from phase I–IV. From supporting first-in-human to global clinical trials, we are prepared to help meet your specific challenges. -
Brochure CMC - Drug substance
Chemical process development includes several stages: from labscale process evaluation through safety and scalability analysis, process optimisation, purification development and solid-state analyses. Our scientific team has extensive knowledge in the development of chemical processes, with a strong focus on process mass intensity (PMI), solid-phase characterisation and impurity profiling. -
Brochure Drug Development - Clinical services
For over 40 years, our CRO has worked closely with pharmaceutical and biotechnology clients to support customised clinical solutions. Our experts provide solutions that meet international standards and deliver relevant strategic insights.



