A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W |
A medical condition which makes a particular drug treatment or procedure advisable in line with the Product License. Drug approvals for specific indications are controlled in most countries and jurisdictions by a licensing body, including the Food and Drug Administration (FDA) in the US and the European Medical Association (EMA) in the EU.
See also:
Food And Drug Administration (FDA)
License (product)
Prescribing information, Clinical, Control group, Food And Drug Administration (FDA), Investigational new drug (IND), Field experiments, New product development (NPD), Disease mongering, Drug-drug interaction, Over the counter (OTC), Open-label trial, Commission on Human Medicines (CHM), European Medicines Agency, International Clinical Trial Registry Platform (ICTRP), Meta analysis,
Company founder Neil Kendle was a pioneer in opinion leader engagement. In 2003, Neil brought together a small, dedicated team...