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Clinical Regulations Services In Usa New Jersey

4 services found
In New JerseyAvailable In New JerseyNear New Jersey

Regulatory Support

Regulatory Support

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 ...
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Medical & Scientific Writing Services

Medical & Scientific Writing Services

by:HingeClinica   based inPrinceton, NEW JERSEY (USA)
Our Medical and scientific Writing team is an integral part of clinical research. Our Medical Writers closely associate with biostatistics, medical affairs, safety and data management teams to deliver accurate, timely, and cost effective deliverables to the highest quality and scientific standards. We have a wide breadth of experience drawn from the pharmaceutical industry and clinical research ...
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Clinical Trial Management Services

Clinical Trial Management Services

by:HingeClinica   based inPrinceton, NEW JERSEY (USA)
Our clinical operations teams have extensive experience in conduct of multicentric global clinical trials in various therapeutic areas. Our team consists of experienced Clinical Managers, CRAs, Medics, Pharmacologists with excellent medical background and in-depth knowledge on clinical trial regulations and ICH ...
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Clinical Trial and Consulting Services

Clinical Trial and Consulting Services

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 ...
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