Analytical Methods (Biopharmaceutical Products)

Coordinating in-process and finished product testing with the completion of batch documentation, we can deliver your drug product within just six weeks of the date of manufacture.

Symbiosis Pharmaceutical Services can manage all of your analytical and microbiologial testing requirements by utili...

Collect all your pharma/biotech data, monitor Pharma OEE and machine utilization, streamline order flow and production execution and achieve operational efficiencies by reducing production costs and increasing throughput

Seamless execution and high-quality results for your early clinical programs. Dedicated to early clinical development, Quotient Sciences can help accelerate your molecule to your first-in-human and proof of concept milestones. We also offer a range of exploratory and regulatory-driven Phase 1 clinical phar...

Max. capacity: 34 m3/h (570 l/min)Max. discharge pressure: 8 bar
Max. temperature: 100 °C
Pump materialss: PE HD1000, PTFE, PP
Certificates: USP VI, FDA, ATEX
Hygienic design and surface uniformityInert and clinically tested materials – no possibility of contamination of the pumped medium
US...

LyoinMSTrack® seamlessly integrates with your existing freeze-dryer, and revolutionizes freeze drying with in-line Mass Spectrometry as a Process Analytical Technology(PAT)，offering real-time, high-precision and non-invasive analysis of moisture, solvent vapor and volatile compounds within the chamber dur...

Customised CMC development and manufacturing for a broad range of advanced biologic modalities. Services include process development, analytical characterisation, scale‑up, and GMP manufacturing, tailored to the characteristics and development stage of each modality.

The loVol®  is a specialized system engineered for low-volume solubility and dissolution testing. Designed for early-stage drug development and formulation screening, loVolr evaluates APIs, powder mixtures, granules, coated pellets, and finished oral dosage forms under both constant pH and dynamic pH ...

Fundamental to your biopharmaceutical chemistry, manufacturing and controls (CMC) development, you will need detailed analytical characterisation data to satisfy regulatory requirements. Our experts strategically deploy orthogonal protein analysis approaches that address key molecular and biological charac...

Lambda provides regulated bioanalytical support for large molecules, biologics and biosimilars across clinical development. Capabilities include large-molecule PK analysis, anti-drug antibody assessment, neutralizing antibody testing, pharmacodynamic biomarkers, functional bioassays, immunogenicity assessm...

Our analytical portfolio comprises 200+ different techniques – all performed by Coriolis’ experts in-house. Our offering includes:
• Aggregate analytics • Particle characterization • Particle identification • Surfactant characterization • Higher order structure analysis • Funcional assays • Chemi...

• 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...

We are a GLP lab specialist in vitro permeation testing, including the bioequivalence tests under the EMA draft guideline. We support pharmaceutical companies through bioequivalence studies. Visit our booth and find out more about our R&D dedicated to this topic.

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...

Automated Technology Platforms:

 
·         E-Scan MicroCurrent HVLDmc  parenterals

·         Vacuum Decay technology for parenterals and other pharmaceutical container format...

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...

Neotron Pharma is able to validate analytical methods developed internally or transmitted by the customer using top of the range equipment such as:
- HPLC-UV / DAD / MSMS
- GC-FID / ECD / MSMS (even in Headspace)
- ICP-MS / AAS / AES / OES
- Post-column derivatization
- Particle si...

Oasis Test House caters to the microbiological requirements for its clients serving them with the below analysis. • Preservative Efficacy Analysis • Sterility Test • Sterility Validation • Microbial Limit Test Validation • Microbial count and pathogens • Bioburden testing • Antibiotics assay • Vitam...

Our GMP-certified in-house laboratory provides integrated analyticalsupport from early development to commercial release. We ensureproduct quality, regulatory compliance, and faster turnaround times.Key Capabilities • Chromatography: GC, HPLC, UPLC, LCMS • Microbiology: USP <51>, <61>, <62&...

Apotek Produktion & Laboratorier AB offers a wide range of analysis services which includes chemical analysis. It can help with chemical and physical/chemical analysis of raw materials for pharmaceuticals and related products. The analysing covers a wide range of preparations such as liquid preparation...

Avara Pharmaceutical Services offers development support services including analytical methods development. Contact us for more information.