Clinical Phase I

API In Capsule Vs. The Lost Art Of Formulation Development

Very few businesses have as specialized a set of needs as those in the pharmaceutical sector. The combination of huge product development costs, large amounts of data and intense regulatory control makes it critical for companies to have needed information as soon as possible in order to meet a varied and closely monitored set of business processes. By Todd Daviau, Ph.D

Brochure: Norwich Clinical Services

Norwich Clinical Services is a contract research organization that provides Bioanalytical Services, Pharmacovigilance and Clinical Research Programs to the pharmaceutical and biotech industries.

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.

Lyophilization Technology, Inc.

Lyophilization Technology provides an extensive range of scientific services and technical support for development and production of pharmaceuticals, biologics, diagnostics, biopharmaceuticals, and medical devices.

Pharma Tech Industries

For more than 35 years, Pharma Tech Industries has built an outstanding reputation as a family-owned business, providing exceptional contract development, contract manufacturing and contract packaging services to the world's leading pharmaceutical, medical devices and consumer products companies.

Uman Pharma Inc.

Uman Pharma is a fully-integrated pharmaceutical company that develops, manufactures and markets generic injectable pharmaceutical products and is the only oncology plant in Canada featuring freeze dryer and pre-filled syringes capacity.

Medical Writing

Writers with both industry and therapeutic expertise
Each member of our core regulatory and medical writing team draws on extensive industry knowledge and therapeutic expertise to effectively meet our clients’ product development requirements and provide top notch medical writing services. Each writer is a graduate-level life science scholar. They enhance their scientific and technical expertise through continuing medical education and study-specific training. Our writers also have access to internal therapeutic experts, researchers, and academics to gain sophisticated insight across many therapeutic specialties. Their experience and training enable them to expertly prepare reports in accordance with regional regulations and ICH Guidelines and to create clinical trial and regulatory documentation suitable for submission to regulatory authorities, including FDA and EMA.

Therapeutic Areas Deep therapeutic knowledge and understanding of the key issues combined with clinical development experience drives more effective and efficient pathways to commercialization.