Good Medicine to all the world!

solidly believes that every individual matters and should have the right to live the healthiest life possible. Our business is modeled after this belief, and through it, we are impacting people’s lives  around the world.

Providing universal access to medicine is the core purpose of our model, pictured below.

To provide access, we must be able to satisfy the needs of an incredibly diversified global marketplace whose economic and political systems, approaches to delivering and paying for healthcare, languages and traditions, and customer and patient requirements vary by location and over time.

In the United States, the Office of Generic Drugs at the Food and Drug Administration follows a rigorous review process to make sure that, compared to the brand-name (or innovator) medications, the proposed generic medications:

• Contain the same active/key ingredient
• Have the same strength
• Use the same dosage form (for instance, a tablet, capsule, or liquid) and
• Use the same route of administration (for instance, oral, topical, or injectable).

FDA’s review process also ensures that generic medications perform the same way in the human body and have the same intended use as the name brand medication. Healthcare professionals and consumers can be assured that FDA-approved generic drug products have met the same rigid manufacturing standards as the innovator drug. In addition, FDA inspects facilities to make certain the generic manufacturing, packaging, and testing sites pass the same quality standards as those of brand-name drugs.