Topicals Manufacturing

The Environmental Impact of Clinical Trials

For many years it has been almost universally accepted that there are various sources that may impact or cause disease among which biological, social, and environmental differences have all been investigated. Many clinical trials have been conducted to assess the impact of the environment on outcomes e.g., the effect of the environment on the outcome of studies assessing the efficacy of drugs for patients with dry-eye syndrome, the impact of diet on obesity and cardiovascular disease, and the impact of the environment on autoimmune diseases have all been studied, as have many other interactions.

Outsourcing Insights: Focusing On Innovation

In 2011, innovation was a major topic among the various players in the drug development industry. By Kate Hammeke, research manager, Nice Insight

Signant Health, formerly CRF Bracket

The best technology succeeds in the background. Signant Health provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials.

Kemwell Biopharma

With manufacturing locations in Bangalore India, and Uppsala Sweden, Kemwell offers the entire value chain from early & late stage drug development services, clinical trial supply support, to commercial contract drug manufacturing.

NextPharma Technologies LTD

NextPharma is a pharmaceutical contract development and manufacturing organisation serving worldwide markets.

3M Drug Delivery Systems Division

3M provides proven inhalation and transdermal solutions at a full range of cGMP global manufacturing facilitiesto help our partners compete effectively.

Paragon BioServices, Inc.

Founded in 1990, Paragon Bioservices is a CMC Center of Excellence delivering research, development and cGMP manufacturing services to pharmaceutical companies, biotechnology companies and federal agencies

 

InVitro Assays SGS provides several in vitro assays to support drug development and testing.

Quality Assurance

Promoting excellence in clinical research
At Rho, Quality Assurance (QA) is an independent group that promotes excellence by ensuring adherence to our processes, applicable regulations, and Good Clinical Practices (GCP). Our auditors’ focus on quality has been honed by years of multidisciplinary clinical research training, from extensive education on topics from software validation to GCP to FDA requirements.