Inthera Blog

Inthera Blog

Pharmaceutical Industry

Designing and conducting a clinical trial from the perspective of the pharmaceutical industry

D: Clinical trial - What aspects should be considered when designing and conducting it from a pharmaceutical perspective? Here are the answers of Inthera!

Pharmaceutical Industry

Good Clinical Practice (GCP): a framework of requirements in human clinical trials

D: Good Clinical Practice (GCP) is an international framework for the conduct and documentation of clinical trials in humans. Learn more from Inthera’s article!

Pharmaceutical Industry

The safety of clinical trials: protecting participants in medical research

D: The safety of clinical trials - Inthera's article summarises how researchers ensure that trials are safe for participants.

Pharmaceutical Industry

What is GLP (Good Laboratory Practice)? - The most important things to know

What is GLP (Good Laboratory Practice), why is it important in the pharmaceutical industry and what are its key principles? Find out in this Inthera article!

Pharmaceutical Industry

The significance of ISO 9001/2015 certification in the pharmaceutical industry

Inthera has obtained ISO 9001/2015 certification. In our blog post, we explain what this means for pharmaceutical industry players.

Pharmaceutical Industry

The clinical trial phase IV: the final stage of the clinical trial

The clinical trial phase IV, the post-marketing study, is the final stage in development. Inthera has complied the key facts about it.