The manufacturing, documentation and marketing of health products
classified as pharmaceuticals are closely regulated and controlled by
health authorities. After their development, these products trigger a
long process during which there are numerous sub-projects ranging from
experimental models and preclinical safety to clinical trials of
escalating dimensions. Alongside the clinical documentation, the
pharmaceutical processes aims to get the best possible formulation for
the product to reach its biological targets.
LINK Medical has expert employees and systems that can provide
integrated services throughout the vast process of pharmaceutical
product development. Our experts assist teams with strategic advice,
handling the projects professionally. Our competence within quality
assurance and regulation will support product development in accordance
with the agreed strategy. We have the people and the plans our customers
need to reach the market with a pharmaceutical product.