Contract Research

Excipients can have an important impact on the manufacturability and pharmaceutical performance of a formulation. It’s therefore important to identify and control functionality related characteristics (FRCs) of excipient materials in order to achieve safe, robust and stable products. Experie...

Solvias has a solid reputation with market-leading biopharmaceutical companies for the characterization and QC analysis of monoclonal antibodies (mAbs), glycoproteins, PEGylated proteins and peptides and biosimilars (follow-on biologics).. This means that businesses of all sizes, even smaller biotechs, can be...

Take no risk with your analytics when developing new therapeutic monoclonal antibodies. Our analytical teams take advantage of their extensive experience in the analysis of mAbs. Throughout non-clinical and clinical development, our experts provide you with the customised solutions in terms of analytical pro...

Discovery Chemistry, Discovery Biology, Integrated Drug Discovery

Inhalation product analysis and testing services include particle size and droplet characterization, delivered dose testing, as well as aerodynamic particle size analysis – for pressurized metered-dose inhalers (PMDI), dry powder inhalers (DPI), nebulizers, and soft mist inhalers. Our Good Manufacturing P...

August Bioservices can support preclinical research needs as well.

These case studies highlight capabilities from cell line development, high-throughput multi-parametric cell health assays, 3D cell culture high content screening, wound healing assays, and mouse models to study colon cancer and lymphoma...

Neotron Pharma is able to offer you a research and development service. The research and development laboratory, operating under the ISO regime, will be able to develop customized methods for the customer in faster times and with lower costs. Subsequently, the customer will be able to validate the GMP method ...

"A reliable and preferred CRAMS (Contract Research And Manufacturing Services) partner in providing innovative Pharmaceutical solutions"

SERVICES OFFERED:* Early phase drug development* Process research and development* CCS (Custom chemical synthesis)* FTE (Full Time Equivalent) based projects&nbs...

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 materials,...

With a full analytical package for Biologics, Quality Assistance provides scientific and technical support to biopharmaceutical companies developing Antibody-Drug Conjugates. Thanks to our combined experience with small molecule cytotoxics and monoclonal antibodies, we can provide full analyt...

Quality Assistance covers all the analytical technologies needed to support your drug development process: CMC (Quality) studies to be perfomed, including Ab characterisation, development and validation of analytical methods, stability studies and batch testing. For Bioanalysis to be performed in Non-clinical...

Cell-based bioassays that comply with cGMP: Using a variety of techniques, including cell-based assays, ligand and receptor binding assays, and flexible multiple assay approaches – our potency testing experts offer tailored bioassay method development, method transfer and method validation to ICH Q2 (R1) s...

Solvias provides wide range of analytical services which includes quality control and release analysis. The analyses are routinely performed at Solvias according to GMP quality standards for drug substances & products, intermediates, starting materials and excipients. Contact us for more information.

Solvias provides expert testing and consulting services for Extractables & Leachables in single-use process materials and container closure systems. With our proprietary EXLEA database, we provide unique automated high throughput screening of more than 6000 Extractablesusing Accurate Mass LC/MS/MS Technol...

Solvias provides high calibre microbiology, chemistry, toxicology and cell biology services according to GMP, CGMP (FDA), GLP and ISO 17025 standards.Testing for sterile and non-sterile products / Environmental testing / Specialised studies (antibiotics, integrity testing, alternative methods) / Endoxin and p...

Solvias provides an integrated and comprehensive approach to solid-state development – from systematic salt, co-crystal, and polymorph screening to controlled scale-up of the crystallization process, all complemented with the full range of physico-chemical studies performed in our laboratories.

Solvias offers the complete range of stability studies according to ICH guidelines for drug development and follow-up stability studies, covering all ICH standard storage conditions as well as low temperature storage. All our processes take place on one connected site, where there is a high degree of QC exper...

Whatever the type of antigen, Quality Assistance covers a wide range of analytical technologies needed to support vaccine development, including product characterisation, development and validation of analytical methods, stability studies, batch testing and bioanalysis to support immunogenicity and ...

Quality Assistance provides extensive experience and state-of-the-art EMA/FDA audited facilities, equipment and software for your Cell-Based Medicinal Products development. We have developed and validated robust, precise and accurate methods to characterise CBMPs in terms of identity, purity and potency....

To meet your analytical needs, Quality Assistance provides you with scientific and technical support for the development of your New Chemical Entities. Our added-value brings together a sound expertise in small molecules analytical development with state-of-the-art facilities and equipment, all on o...