Journal Marti Farm

19 APRIL, 2023. Change is what makes us push boundaries. As our medicines keep evolving, so do Clinical Trial procedures.31st January 2022 marked the start of the transition period that changes the way we submit, authorize, and supervise CTAs. By 31st January 2023...

With marketing authorization application, the applicant is obligated to submit the dossier in the form of an Electronic Common Technical Document (eCTD).

The COVID-19 pandemic impacted every aspect of our lives, including the way we conduct business. Audits are no exception. Remote auditing was already gaining prominence in the last decade.

The regulatory journey of your product does not end with its placement on the market: regular marketing authorisation renewals are also required

An audit is a systematic and independent process for gathering objective evidence and its objective assessment to determine the extent to which auditing criteria are met.

Labeling and packaging development is a combination of regulatory, linguistic, commercial, and design expertise. A range of differing factors impact the quality

One of the most significant aspects is trial location. From the number of patients to the local regulations, clinical trials are highly impacted by location.

On 22 March 2020 Zagreb was struck by a 5.5 magnitude earthquake. More than a hundred aftershocks followed, and more than 7000 buildings were damaged.

Apoptosis is a form of programmed cell death carried out in a series of highly organised biological processes.