Clinical Trials Phase I to IV

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...

.Integrated drug development service (CRO/CDMO) including clinical manufacturing and management.
The range of activities offered by Bluepharma includes:
- Clinical material cGMP manufacturing
- Clinical supply management
- clinical material
- placebo
- ...

• 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 s...

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

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

CARBOGEN AMCIS has a DNA in API development, stretching back over 30 years. Our API development teams are selected for their passion for science and experience in the application of phase-appropriate efforts to solve challenging chemistry issues. From taking a promising molecule from our clients' medi...

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
• Technolog...

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.

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 o...

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 st...

At ProRelix Research, our dedicated clinical trial project management team provides Phase 1, 2, 3, and 4 clinical research services in compliance with the principles of ICH & GCP, trustworthy clinical safety services, site selection based on their history of meeting enrollment targets, and consistent d...

Our in-house cost-effective Digital solutions keep you connected at every stage, no matter where in the world your studies run.

Our Digital Solutions are integrated solutions, Regulatory compliant, and it can handle all type of clinical trials.

Our Digital Solution portfolio consist o...

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. A...

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 stud...

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), Bacteri...

•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 manufactu...

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

Gamma scintigraphy is a powerful and versatile technology used to investigate the in-vivo performance of your drug or product. This non-invasive imaging technique allows us to follow the fate of the dosage form and administering it to a volunteer or patient. Not limited to just oral dosage forms, gamma sci...

Our nets community is the place to discuss trends, insights, and future solutions. The philosophy behind each network is to:

• Provide a platform for industry peers to learn and share from one another in an open environment • Deliver benchmark information to compare and measure operational ...

At Navitas Life Sciences our experienced consulting team delivers strategy and change management programs to our clients. We are a leading life sciences consultancy with global reach and some 25 years of experience. We are proud of our track record of results with clients focusing on Patient Safe...

As a proven full services provider, Navitas Life Sciences brings our rich experience from partnering with well over a 100 innovator and generic Life Sciences companies to conduct a significant number of studies, including Phases 2 – 4, NIS, Biosimilars, and BA/BE. We have been a partner of choice for...