Clinical Trials Phase I to IV

Recipharm have more than 20 years experience supplying clinical trial material to our clients. Our development facilities cater for a range of clinical trials from preclincal to smaller Phase III trials. We also offer commercial manufacturing for very large clinical batches.

Services for Bioanalysis (GLP/GCP): In our state-of-the-art facilities, we provide GLP/GCP method development, validation, method transfer, sample analysis and pharmacokinetic and toxicokinetic support, along with automated data collection and reporting systems. Over the past 20 years, we have supported th...

The period from preclinical through Phase III is pivotal and sometimes unpredictable for new molecules, particularly today’s complex compounds. With Vetter Development Service, you have a partner you can trust to support you throughout drug product development, clinical manufacturing, and regulatory approval....

GenIbet runs projects covering a broad spectra of Biopharmaceuticals development, including Recombinant proteins, Vaccines, RNA, Live Microbial Products and Cell and Gene Therapy products. GenIbet has experience with mammalian, avian and insect cells (A549, CAP, CHO, EB66, HEK293, SF9, MDCK, Vero), Bacteria a...

When you are looking for a partner who is dedicated to Phase I trials and early clinical development, rely on Quotient Sciences for the experience and expertise to seamlessly deliver your studies with the highest quality service and speed. We accelerate your molecule from first-in-human to proof-of-concept, h...

• Mumbai / Ahmedabad / Hyderabad • 24hr operations 7 days per week, 365 days per year • GDP compliant warehouses in Mumbai • Walk in cold chain facilities for high volume supply of temperature controlled packaging Pre filled Dry shippers for next day supply • Active and passive bulk container spec...

TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing

GALENIC DEVELOPMENT
• Preformulation studies.
• Design and galenic developmen...

Setting the stage for the commercial process:• Route or step rebuild
• Process optimization &demonstration
• Impurities assessment & synthesis
• Full structure characterization &elucidation
• Analytical method development &qualification
• Stress studies & ICH stability stand...

•  Pro-active and flexible system of project management
•  Comprehensive reporting system
•  Additional labeling
•  Returns/recalls
•  All temperature-controlled regimes
•  Temperature and humidity monitoring system
•&...

Our monitors perform on-site clinical trial monitoring visits throughout the length of the study to oversee the collection of data; review clinical laboratory results, source documentation and electronic/paper case report forms; resolve data queries; and confirm regulatory compliance
Our Monitoring Capab...

GenIbet Biopharmaceuticals is a GMP biopharmaceutical CDMO offering highly specialized GMP manufacturing and development services to research groups, Biotech and Pharma companies. GenIbet core activity is the manufacture and supply of materials for use in early stage drug development, pre-clinical studies...

Understanding that early phase clinical testing is a pivotal milestone in the development of your drug product, Quotient offers a clinical trial manufacturing, testing and certification service designed to meet your individual requirements. Our innovative method of building integrated GMP and GCP programs pro...

TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract ManufacturingPilot

Batches and Registration Batches /
• Manufacture in compliance with the principles and guidelines of GMP for medicinal products.
• Transfer of a...

Taking the molecule to market• Fate & purge studies
• Impurities marker synthesis &qualification
• Design of experiments
• Critical process parameters studies
• Preparation for, and execution ofprocess validation
• Continuing CMC support during &after market launch
• Technology t...

Our expert teams help eliminate delays by leading the way from recruitment strategies, medical writing, and clinical logistics, all the way through the regulatory process.

Our in-house eClinical technologies keep you connected at every stage, no matter where in the world your studies run. And with ...

Our Home Nursing service brings the clinical trial directly to the patient. This service allows PI and SI to administer treatments and monitor outcomes in the comfort of the patient’s home. This eliminates the inconvenience of travelling to a site for the patient and may also have benefits for sponsors by...

Intertek offers wide range of pharmaceutical services which includes bioequivalence studies. It belongs to bioanalytical services for preclinical and clinical studies category. Contact us for more information.

Intertek offers wide range of pharmaceutical services which includes large molecule bioanalytical services. It includes immunochemistry services, quantitative immunoassays, immunogenicity assays, biomarkers assays and validation, cell-based neutralization assays, ligand-binding assays, etc.

BizNET-CTM, an end-to-end platform for clinical trials; right from Early phase, Late phase, Oncology to Registry to Post approval trials.

Suite of solutions for Clinical Research:

> eCRF, EDC and Clinical Data Management
> IWRS and Pharmacy Management
> Medic...

•SWIFT accelerates evaluation and optimisation of product performance using in vivo clinical data to direct formulation design in real time.
•SWIFT studies enable you to make decisions on formulation changes based on emerging clinical data. • This integration of formulation development, GMP manufacturin...