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Clinical Candidate Developed Services In Usa New Jersey
10 services found
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
Our Biostatistics & SAS programming team has global experience in clinical trials start right from the protocol design to Final analysis. Our team consists of highly educated, professional with Biostatics and SAS programming and has in depth knowledge in ICH GCP, ICH E9, CDISC, CDASH and SDTM standards. We offer full range of integrated, global, therapeutically aligned Biostatistics services ...
Manufactured by:Rocket Pharmaceuticals, Inc. based inCranbury, NEW JERSEY (USA)
Rocket’s Research and Discovery group in the Cranbury, New Jersey facility utilizes approximately 20,000 square feet of state-of-the-art laboratories for designing, optimizing and advancing candidate therapeutics to clinical stage ...
by:Solvias AG based inKaiseraugst, SWITZERLAND
Preformulation Package: Preformulation includes the compiling of solubility profiles (pH dependent and other systems of interest), permeability (logP/D, CaCo2 or other cell-based assays), BCS classification, accelerated chemical stability, basic physico-chemical parameters like pKa, melting point, hygroscopicity, salt screening, and polymorphism ...
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
Our Project Management team has extensive experience in clinical trials project management right from the project kick-off to project closure. Our team consists of highly educated and Project Management certified professional in clinical trial end to end project management. We manage your clinical trials start from the protocol development to Final report submission. Ensuring deliverables are met ...
Manufactured by:Jubilant Therapeutics Inc. based inBedminster, NEW JERSEY (USA)
Jubilant Therapeutics is open for partnering or strategic. collaborations with biotech, pharma, academia, research labs for: Accelerating clinical development and market launch of our ongoing programs. Discovery/development of new programs in synergistic areas. Conducting research with our drug candidates either as monotherapy ...
Manufactured by:Regenity based inParamus, NEW JERSEY (USA)
Securing approvals can be challenging amid a shifting regulatory landscape. With a deep history in collagen-based products and polymer science, we support our clients through global regulatory submissions, claims development, as well as clinical study and protocol development consultations. With years of experience designing preclinical and clinical studies for regenerative devices, our team is ...
by:Freyr Solutions based inPrinceton, NEW JERSEY (USA)
After years of successful clinical research, submission of documents for Health Authority (HA) review requires a specialized skill of clear and precise clinical report writing. Such clear and precise clinical writing aids reviewers to easily comprehend the technicalities of clinical research, as a single error in clinical documentation may prove risky and costly for organizations, causing delays ...
Manufactured by:Cambrex Corporation based inEast Rutherford, NEW JERSEY (USA)
Cambrex has extensive experience in Drug Metabolism and Pharmacokinetic (DMPK), Bioanalytical and Biopharmaceutical Analyses. The Biopharmaceutical Analyses scope supports GMP method development, validation, and routine analysis including but not limited to host cell proteins, host cell DNAs, endotoxins, enzyme kinetics, and even bacteriophage titering assays. The Drug Metabolism and ...
by:HingeClinica based inPrinceton, NEW JERSEY (USA)
HingeClinica is a world class partner for Medical Device services. We render End to End Medical device MDR compliance and Regulatory services, Clinical trial, Pharmacovigilance services to Medical Devices industry. Our Medical Device team has extensive experience in working with US FDA, EMA, PDMA, SFDA, Health Canada, DCGI and ROW, regulatory Submissions and ...
Manufactured by:Cambrex Corporation based inEast Rutherford, NEW JERSEY (USA)
We work closely with biotech start-ups and established biopharma companies to evaluate the quality, purity, safety and other key attributes of candidate viral therapies and large molecules at all phases of the preclinical and clinical development pipeline. We offer a comprehensive suite of testing services for complex biopharmaceutic products, ...