Analytical Chemistry (Biopharmaceutical Products)

cUSP - Ready to use standard solutions for Analytical / QC chemist, Analyst , Scientist.  cUSP products are known for their Reliability, Reproducibility, Repetitive results, Consistence results in each analysis.  cUSP series of products are manufactured under strict ISO standards. cUSP products a...

SGS Life Sciences has considerable expertise in the method development of nitrosamine determination in pharmaceutical products. SGS has established a specific method for NDMA which can be applied to various different matrices. Alternatively, a platform method, based on trace-level detection by LC-MSMS, is ...

Physico-Chemical testing
- General identification (TLC, HPLC)
- Assay (UV/VIS, HPLC-UV, GC-FID, LC-MS/MS) and dosage uniformity
- Related substances identification and quantification (HPLC-UV, GC-FID, LC-MS/MS)
- Physical determinations (pH, viscosity, density)
- Moisture...

• GMP Release Testing Services • Product Characterisation • Occupational Hygiene Analysis • Purity Profiling & 5 Batch Studies • Extractables & Leachables • Material Characterisation • Stability Testing Services • Physico-chemical Properties • De-formulation

Clearsynth provides a wide range of high-purity NMR solvents designed to ensure optimal resolution and reliable analysis, supporting both research and quality control applications 

Benzene D6 , Chloroform-D , Dimethyl Sulphoxide D6 (DMSO D6) , Methanol D4 , Deuterium Oxide , Tetrahydrofuran...

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...

• 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...

Sterile sodium hyaluronate
The raw materials of sterile sodium hyaluronate produced by the sterile production process can be used directly by downstream manufacturers for sterile preparations and sterile medical devices without further sterilization procedures.

    ·&nbs...

To support you in bringing even safer medicines to the market, we go far beyond supplying you with the right reference standards. From impurity profiling and working standards outsourcing services, all the way to managing inventory and logistics of your reference standards, we’re fully equipped to provide ...

We celebrate the arrival of our synTQ by Optimal NMR adapter – opening the door to a new world of PAT for the Bruker Fourier 80. This brings a wealth of structural information and direct quantification to online chemical and bioprocess monitoring, resulting in further reductions in risk and cost.

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

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...

HPLC columns from VDS optilab have been impressed customers from all areas of analytics, ranging from universities and government agencies to small and medium-sized companies and large companies in the chemical and pharmaceutical industries. Benefit from the advantages of the VDSpher phases product fa...

Accelerating molecules through to proof-of-concept - Simplify early development and accelerate to Proof-of Concept.Proof-of-concept (POC) is a key milestone in the development of a new drug candidate. We understand the transition to POC needs to be fast and cost-effective.With fully integrated capabil...

Our expert team provides full analytical, microbiology and stability services to ensure that your raw materials, bulk product and finished products are qualified, analyzed and released to cGMP standards.

Our services include:

Analytical
• Raw material and drug product...

We offer a highly professional quality management throughout the organization. In more than 500 m² of laboratory facilities, we annually test approx. 1,500 product Batches . The area of responsibility for quality control already starts with choosing the appropriate suppliers. Hence, in...

UDP-Gal is a nucleotide sugar consisting of the nucleotide uridine 5'-diphosphate and a phosphate-bound monosaccharide, α-D-galactose. Nucleotide sugars are the activated forms of monosaccharides required for cellular metabolism and biosynthesis reactions. UDP-gal serves as a donor substrate for galactosyl...

Largest synthetic acetonitrile and high purity solvents manufacturer. • 35,000 t/a synthetic acetonitrile ; • 25,000 t/a high purity acetonitrile ; • 10,000 t/a HPLC solvents ; • 10,000 t/a solvent blending and packaging capacity.

Rare cannabinoids：CBC Series/CBG Series/CBD Series(CBC/CBCV/CBG/CBGP/CBDV/CBDB/CBDH/CBDP/CBDC8