What DeepC knows.

Regulations

Guidelines, approval packages, assessment reports, labels and product information from medicines agencies around the world, read section by section with their figures.

Excipient and pharmacopoeial standards

Excipient grades and the levels already accepted for each route and dosage form, recommended dissolution conditions, and the harmonised pharmacopoeial texts.

Approved products

What is already authorised, and where: national product registers, the excipients declared in approved labels, and inspected manufacturing sites.

Toxicology and safety

Toxicology studies, reference doses, exposure limits and hazard classifications, with adverse event reports from use in patients.

Clinical trials

Trial records with their design, eligibility, sponsors and outcomes, and the protocols and analysis plans behind them.

Literature

The biomedical literature, and the web for anything newer, cited like everything else.

Patents

Patents across the major jurisdictions, with their claims and families, for freedom to operate and for drafting.

Physicochemical data

Physicochemical properties and identifiers for drugs and excipients, with descriptors, solubility and drug-likeness calculated on demand.

Biologics

Approved biologics and biosimilars, antibody structures and sequences, protein references and lipid nanoparticle formulations.

Your documents

Your organisation’s library, your own references, project files and connected Microsoft 365 libraries, with each person’s permissions respected.