Method Validation

From early development, including mammalian cell line development, cell culture development, and process development, through to pre-clinical production and commercial supply, Patheon by Thermo Fisher Scientific provides CDMO services for protein-based biologic therapeutics. Patheon offers biotech and ...

LabAnalysis is a family owned CRO offering innovative and reliable solutions to Quality Controls andResearch and Development Departments. Customer Care and Commitment to Quality are the driving forcesfor our continuous and sustainable growth with a proven track record of long last business partnershipsarou...

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

We offer the development and validation of test methods for identity testing, assay, purity testing and in vitro dissolution for active ingredients, excipients, intermediates, finished products and substance-based medical devices. Our method development and method validation are in accordance wit...

Früh Laboratory Services provide accredited testing and validation for medical device packaging systems. From planning and design validation through to final validation reports, we ensure compliance with international standards. Our laboratory offers integrity testing, material and packaging analysis, and ...

Analytical methods development & validation: We apply a broad range of analytical technologies - including chromatography, mass spectrometry, spectroscopy, biophysical and bioanalytical techniques - across diverse products and methods - to ensure every method is fit for its intended purpose.
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Our mission is to deliver outstanding pharmaceutical services at affordable prices, with an emphasis on speed, accuracy, and clear communication, ensuring every client receives dependable results and a seamless experience.

We invite attendees to visit Booth 915 to discuss how CRC Labs can...

GMP analyticsQuality control of raw materials, excipients, active pharmaceutical ingredients (APIs), and finished medicinal products
Batch release (EU retest)
Method validation, verification, and transfer
Biopharmaceutical studies
Human and veterinary sectors

Nelson Labs offers a full trifecta of services to meet the requirements of ISO 10993 for Extractables & Leachables, Biocompatibility and Toxicological Assessments of medical devices. Biocompatibility testing is very common in the medical device industry. However, with 24 possible categories, each with...

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...

testo Saveris - Data monitoring systems with automated and uninterrupted measurement data recording of temperature and humidity values in the environment and in processes. Offers centralized documentation as well as an alarm function thusly saving time. It guarantees the safety of your measurement data...

Generic manufacturers registering into CARICOM run their bioequivalence studies outside the region or through a small number of bridging facilities elsewhere in the Caribbean. Either route adds cost and schedule to every submission, with in vivo studies running to six figures per product.

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Curida offers Lab services1 chemical lab 
3 microbiological labs, including sterility lab and lab for test organisms


Main services:
Quality Control 
Method development and validation 
Stability testing 
Contract laboratory

Lambda offers integrated laboratory services supporting clinical development and biosimilar programs, with capabilities spanning regulated bioanalysis, biosimilar characterization, immunogenicity testing, microbiological testing, and central clinical laboratory services. Bioanalytical capabilities support ...

At PLD Pharma Services our analytical testing lab is also a development lab where we develop and optimize analytical methods that are robust and QC-friendly. We ensure that methods are efficient, reproducible, and aligned with both regulatory expectations and commercial manufacturing needs. 
q...

Nelson Labs Europe offers a comprehensive approach toward Extractables & Leachables testing for the pharmaceutical industry. Our approach combines technical and analytical expertise, polymer knowledge and understanding of regulatory requirements, all combined in a tailored approach for our customers.

• Multiple MOC swab frame • Multiple MOC swab frame with handle • Telescopic device for holding swab frame • Telescopic device for holding swab stick • Telescopic device with mirror and torch • Multiple MOC swab templates

Our GMP compliant laboratories provide pharmaceutical impurity testing for new drug substances (ICH Q3A(R2)) and new drug products (ICH Q3B(R2)) that can support your product development from an early stage and across the lifecycle of your drug product. Our scientists are adept at method routinely overcome...

Nelson Labs Europe offers a comprehensive approach toward Extractables & Leachables testing for the pharmaceutical industry. Our approach combines technical and analytical expertise, polymer knowledge and understanding of regulatory requirements, all combined in a tailored approach for our customers.

Manufacturing facilities and processes can be a primary source of product contamination. Nelson Labs offers a range of services to assess these manufacturing environmental conditions, in addition to water system validations, raw material screening and residual manufacturing material tests.